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Donor Profile : Donor 5684

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Advisory

Retired Donor

This donor is no longer active in the program. The number of vials available represents the remainder of the donor's inventory.

Donor ID: 5684

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Meet The Donor

A day hike and a steak dinner make a good day for Donor 5684! Ambition and determination were the driving forces that guided Donor 5684 2,193 miles as he hiked the Appalachian Trail. This was one of his biggest challenges and most proud accomplishments. Donor 5684 attributes overcoming challenges such as this to his unwavering discipline leading to his success. He is skilled in digital design and software engineering and is intrigued by electric cars and rockets!

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Genetic Testing Performed: Please review the list of genetic tests performed before choosing a donor because donors have different levels of testing. Genetics is very complicated and testing can only reduce but not eliminate the risk of a donor being a carrier of a particular condition.


Any potential new health information will be indicated here. Please check periodically for medical updates. This profile is current as of:
July 16, 2025 7:48 AM EST


Document ID: 2D3912FACF2823375F2F3127718F305BF501455A06D7D943F97A4315D25B07FB

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Donor's "Name": Xander

Year of Birth: 2002

Marital Status: Single

Number of Children: 0

Occupation:
(last reported) College Graduate

Education: Bachelor of Science, Computer Science

Blood Type: AB +

Nationality:
(self reported) Maternal: English
Paternal: English

Race: White Or Caucasian

CMV Status: NEG
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Last Medical History Update: 04/24/2025

  • Reported Pregnancy/Birth
  • xyIdentity Disclosure
  • Available Inventory
  • Retired
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ADDITIONAL DONOR DETAILS

  • Height:
    5'11" (180.34 cm)
    Weight:
    165 lbs (74 kg)
    Eye Color:
    Blue
    Hair Color:
    Blonde, Dark
    Hair Texture:
    Coarse
    Hair Loss:
    None
    Hair Type:
    Straight
    Dominant Hand:
    Right
    Hairy Chest:
    Yes
    Hairy:
    Yes
    Ear Lobes:
    Attached
    Beard Color:
    Blonde, Dark
    Eyebrows:
    Medium
    Dimples:
    Yes
    Acne:
    No
    Acne Information:
    Shoe Size:
    10
    Body Build:
    Medium
    Freckles:
    None
    Skin Tone:
    Fair
    Face Shape:
    Oval
    Lips:
    Normal
    Nose Shape:
    Normal
    Long Eyelashes:
    No

  • Challenges are part of life that cause you to reconsider, grow, adapt, and overcome struggles which often lead you to become a better and wiser person. For this reason, I have always looked at challenges and struggles to be essential. There are multiple instances where most would say that I strayed from the normal path in my teenage years that allowed me to grow and learn as a young adult. My most proud accomplishment was multiple years in the making and is a type of endeavor that is worth highlighting.
    I grew up in an area without mountains, seasons, or much terrain. I really enjoyed what we had, it was coastal, and watersports were often on the agenda. My parents encouraged my brother and I to always be involved in a sport and ensure we got enough time outside. My brother and I have and always have had a close relationship with my parents, and with each other, only being a year and a half apart. Often the two of us would tend to want to join my father in his adventures. One year, my dad joined a group of guys on a week-long trip to the mountains. They were going to go backpacking on a section of the Appalachian Trail during the summer. You can probably imagine the jealousy of two early teenage boys watching their father go hiking, out of state, to the mountains which we have never explored. A few years later we convinced him to take us along on the adventure. The first few trips we went on, we had our fair share of challenges. The Appalachian Trail is a tough trail, it’s 2,193 miles long, travels through 14 states, and has many other significant statistics. While on the trail, we met people doing a so-called “Thru-Hike” of the entire trail. This meant that they were going to hike all 2,193 miles during a single calendar year! I thought of them as legends at camp. Since that moment, I knew it was something I wanted to accomplish.
    With the goal in mind of successfully becoming a Thru-Hiker, I had some challenges to consider. I needed to allocate time for what is often a 6-month adventure, learn everything there is to know about backpacking gear and safety, convince my parents that I could handle it, and lastly, I needed to fund the trip. Our yearly trips turned into my training, providing plenty of time to understand what you do and don’t need to bring onto the trail, as anything you want to bring is carried on your back. Allocating the time is tough, imagine trying to take 6 months off work to hike a trail. Luckily, I took advanced classes in high school and was able to graduate a year early. This allotted me the time to work and purchase everything I would need, and to complete the trip while staying on the same timeline for college as my peers. Convincing my parents was relatively simple, I had to be 18, which I turned a week before setting off on my adventure. Once they were okay with it, I had their full support. This adventure is something my dad would have loved to do, so he was there every step of the way.
    My parents took me to the start of the Appalachian Trail, hiked a few miles with me and we said our goodbyes. This was a very tough moment for me. As a young adult who was dreaming of accomplishing this goal and had thought that I planned every step of the way was immediately hit with an awakening of reality. I’m hugging both of my parents at a fork in the trail, where I’m going to leave one way and my parents will be heading the other. It’s like dropping your child off at college, except they’ll be living in the woods with other strangers, and they may or may not have cell service. That was a significant point in my life that has developed who I am today. About a month down the trail, I was hit with another fork in the road along with the rest of the planet. The news of COVID was accruing, and things started to get weird. The small towns I came to had less and less food as shipments slowed down, meaning it would be tougher and tougher to resupply. My parents left the decision to me but encouraged me to let them pick me up. I agreed. This is one of the moments that I’ll always remember about their ongoing support for my endeavors. At a moment’s notice they drove through multiple states to pick me up and take me home. Although less significant than the pandemic that was occurring, my dream now felt like a possible failure.
    Two months later, the small towns I would need to resupply in became more stable as the world adjusted. We decided that it would be okay to continue my adventure. Once again, at a moment’s notice my parents drove me back to where they picked me up, we said our goodbyes and I was off. Now I have a new challenge, I did not prepare for this 2-month break, and my first college semester was approaching. To complete the trail prior to college, I had to average 22 miles per day over the mountainous terrain for the next 1,800 miles. My previous average was approximately 12 miles per day, as I had plenty of time on my hands. This was particularly difficult because it did not account for breaks. If I wanted a day off hiking to spend in town, I would have to make up that mileage somewhere. I find myself to be quite a disciplined person, and when I set my mind to something, I really set my mind to it. My first couple of days back were approximately 17-mile days, and I soon increased that to where my goal was a minimum of 22 miles, and if I could go further than I did. My furthest day was 34 miles. Towards the middle of September my parents purchased their plane tickets to come meet me at the northern terminus in Maine, 14 states away from where I started. We hiked the final mountain together and it was the most incredible feeling. My dad was my eyes in the sky, he kept an Excel sheet of where I was on what day, how many miles I completed, with notes about what I mentioned to him.
    After the hike, we talked about their thoughts of sending me back to the trail with what seemed like an impossible deadline. They had told me things like “just have fun and make the most of the time that you have” soon after taking me back, knowing that I would have been tough on myself if I wasn’t able to complete my goal. This was incredibly encouraging to me, even though they knew the odds were stacked against me, they kept encouraging me and showed me that I had their full support. For that reason, the preparation, execution, and challenges of the hike is one of the most influential and important parts of my life.

    Sincerely,
    Donor 5684

  • ADVISORY

    This donor is a carrier of one or more genetic conditions.

    The list below includes the condition(s) that the donor carries. To view a complete list of the genes included in the donor's carrier testing click the relevant link below. To download the donor's test reports click the relevant link below. To purchase this donor's sperm, the intended parent/recipient must sign an acknowledgement form. For more information, please contact us.

    Over the years, Xytex has expanded genetic testing of donors as genetic knowledge and technology have advanced. As a result, not all donors have been tested for the same conditions or with the same methods. For more information about genetic testing view our Genetics FAQs.

    This donor has been evaluated for carrier status of the listed conditions. A negative result reduces, but does not eliminate, the likelihood of the donor being a carrier. If you are a known carrier of a genetic condition, please use the advanced search features to find donors who have tested negative for the condition(s) that you carry. Click the relevant link below to download the donor's test reports to share with your physician and/or genetic counselor.

    This donor's carrier testing included 569 genes.

    Alpha-Thalassemia (HBA1/HBA2)
    Silent carrier (aa/a-)
    Medium/Short-Chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency (HADH)
    Carrier
    Usher Syndrome Type IIA (USH2A)
    Carrier
    17-Beta Hydroxysteroid Dehydrogenase 3 Deficiency (HSD17B3)
    No disease-causing variants detected
    2-Methyl-3-Hydroxybutyric Aciduria, X-Linked (HSD17B10)
    No disease-causing variants detected
    21-Alpha-Hydroxylase-Deficient Congenital Adrenal Hyperplasia (CYP21A2)
    No disease-causing variants detected
    3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (HMGCL)
    No disease-causing variants detected
    3-Methylcrotonyl-CoA Carboxylase Deficiency, MCCC1-Related (MCCC1)
    No disease-causing variants detected
    3-Methylcrotonyl-CoA Carboxylase Deficiency, MCCC2-Related (MCCC2)
    No disease-causing variants detected
    3-Methylglutaconic Aciduria Type III also known as Costeff Optic Atrophy (OPA3)
    No disease-causing variants detected
    3-Phosphoglycerate Dehydrogenase Deficiency, PHGDH-Related (PHGDH)
    No disease-causing variants detected
    6-Pyruvoyl-Tetrahydropterin Synthase Deficiency (PTS)
    No disease-causing variants detected
    ABCA3-Related Disorders (ABCA3)
    No disease-causing variants detected
    ABCA4-Related Disorders (ABCA4)
    No disease-causing variants detected
    Abetalipoproteinemia (MTTP)
    No disease-causing variants detected
    Achromatopsia (CNGB3)
    No disease-causing variants detected
    Acrodermatitis Enteropathica (SLC39A4)
    No disease-causing variants detected
    Acute Infantile Liver Failure (TRMU)
    No disease-causing variants detected
    Acyl-CoA Oxidase I Deficiency (ACOX1)
    No disease-causing variants detected
    Adenosine Deaminase Deficiency (ADA)
    No disease-causing variants detected
    ADGRV1-Related Disorders (ADGRV1)
    No disease-causing variants detected
    Adrenoleukodystrophy, X-Linked (ABCD1)
    No disease-causing variants detected
    Agammaglobulinemia, X-Linked (BTK)
    No disease-causing variants detected
    AHI1-Related Disorders (AHI1)
    No disease-causing variants detected
    Aicardi-Goutieres Syndrome (SAMHD1)
    No disease-causing variants detected
    Aicardi-Goutieres Syndrome 2 (RNASEH2B)
    No disease-causing variants detected
    Aicardi-Goutieres Syndrome 3 (RNASEH2C)
    No disease-causing variants detected
    Aicardi-Goutieres Syndrome 4 (RNASEH2A)
    No disease-causing variants detected
    Aldosterone Synthase Deficiency also known as Corticosterone Methyloxidase Deficiency (CYP11B2)
    No disease-causing variants detected
    ALG13-Related Disorders, X-Linked (ALG13)
    No disease-causing variants detected
    Alkaptonuria (HGD)
    No disease-causing variants detected
    Alpha-1 Antitrypsin Deficiency (SERPINA1)
    No disease-causing variants detected
    Alpha-Mannosidosis (MAN2B1)
    No disease-causing variants detected
    Alpha-N-Acetylgalactosaminidase Deficiency (NAGA)
    No disease-causing variants detected
    Alpha-Thalassemia Intellectual Disability Syndrome, X-Linked (ATRX)
    No disease-causing variants detected
    Alport Syndrome, COL4A3-Related (COL4A3)
    No disease-causing variants detected
    Alport Syndrome, COL4A4-Related (COL4A4)
    No disease-causing variants detected
    Alport Syndrome, X-Linked (COL4A5)
    No disease-causing variants detected
    Alstrom Syndrome (ALMS1)
    No disease-causing variants detected
    Andermann Syndrome (SLC12A6)
    No disease-causing variants detected
    Androgen Insensitivity Syndrome, X-Linked (AR)
    No disease-causing variants detected
    Arginase Deficiency also known as Argininemia (ARG1)
    No disease-causing variants detected
    Argininosuccinic Aciduria (ASL)
    No disease-causing variants detected
    ARL6-Related Disorders (ARL6)
    No disease-causing variants detected
    Aromatase Deficiency (CYP19A1)
    No disease-causing variants detected
    Arthrogryposis, Mental Retardation, and Seizures (SLC35A3)
    No disease-causing variants detected
    ARX-Related Disorders, X-Linked (ARX)
    No disease-causing variants detected
    Asparagine Synthetase Deficiency (ASNS)
    No disease-causing variants detected
    Aspartylglucosaminuria (AGA)
    No disease-causing variants detected
    Ataxia With Vitamin E Deficiency (TTPA)
    No disease-causing variants detected
    Ataxia-Telangiectasia (ATM)
    No disease-causing variants detected
    Ataxia-Telangiectasia-Like Disorder 1 (MRE11)
    No disease-causing variants detected
    ATP8B1-Related Disorders (ATP8B1)
    No disease-causing variants detected
    Atransferrinemia (TF)
    No disease-causing variants detected
    Autosomal Recessive Congenital Ichthyosis, ABCA12-Related (ABCA12)
    No disease-causing variants detected
    AVPR2-Related Disorders, X-Linked (AVPR2)
    No disease-causing variants detected
    Bardet-Biedl Syndrome, BBS1-Related (BBS1)
    No disease-causing variants detected
    Bardet-Biedl Syndrome, BBS10-Related (BBS10)
    No disease-causing variants detected
    Bardet-Biedl Syndrome, BBS12-Related (BBS12)
    No disease-causing variants detected
    Bardet-Biedl Syndrome, BBS2-Related (BBS2)
    No disease-causing variants detected
    Bardet-Biedl Syndrome, BBS4-Related (BBS4)
    No disease-causing variants detected
    Bardet-Biedl Syndrome, BBS5-Related (BBS5)
    No disease-causing variants detected
    Bardet-Biedl Syndrome, BBS7-Related (BBS7)
    No disease-causing variants detected
    Bardet-Biedl Syndrome, BBS9-Related (BBS9)
    No disease-causing variants detected
    Barth Syndrome, X-Linked (TAZ)
    No disease-causing variants detected
    Bartter Syndrome Type 1 (SLC12A1)
    No disease-causing variants detected
    Bartter Syndrome Type 2 (KCNJ1)
    No disease-causing variants detected
    Bartter Syndrome, Type 4A (BSND)
    No disease-causing variants detected
    Bernard-Soulier Syndrome, Type A1 (GP1BA)
    No disease-causing variants detected
    Bernard-Soulier Syndrome, Type C (GP9)
    No disease-causing variants detected
    Beta-Ketothiolase Deficiency (ACAT1)
    No disease-causing variants detected
    Beta-mannosidosis (MANBA)
    No disease-causing variants detected
    Beta-Thalassemia, Sickle Cell Disease, and Beta-Globin Disorders (HBB)
    No disease-causing mutations detected; normal hemoglobin analysis
    Biopterin-Deficient Hyperphenylalaninemia, PCBD1-Related (PCBD1)
    No disease-causing variants detected
    Biopterin-Deficient Hyperphenylalaninemia, QDPR-Related (QDPR)
    No disease-causing variants detected
    Biotin-Responsive Basal Ganglia Disease (SLC19A3)
    No disease-causing variants detected
    Biotinidase Deficiency (BTD)
    No disease-causing variants detected
    Bloom Syndrome (BLM)
    No disease-causing variants detected
    BRIP1-Related Disorders (BRIP1)
    No disease-causing variants detected
    Brittle Cornea Syndrome, PRDM5-Related (PRDM5)
    No disease-causing variants detected
    Brittle Cornea Syndrome, ZNF469-Related (ZNF469)
    No disease-causing variants detected
    Canavan Disease (ASPA)
    No disease-causing variants detected
    Carbamoylphosphate Synthetase I Deficiency (CPS1)
    No disease-causing variants detected
    Cardioencephalomyopathy (SCO2)
    No disease-causing variants detected
    Carnitine Palmitoyltransferase IA Deficiency (CPT1A)
    No disease-causing variants detected
    Carnitine Palmitoyltransferase II Deficiency (CPT2)
    No disease-causing variants detected
    Carnitine-Acylcarnitine Translocase Deficiency (SLC25A20)
    No disease-causing variants detected
    Carpenter Syndrome (RAB23)
    No disease-causing variants detected
    Cartilage-Hair Hypoplasia (RMRP)
    No disease-causing variants detected
    Catecholaminergic Polymorphic Ventricular Tachycardia, CASQ2-Related (CASQ2)
    No disease-causing variants detected
    CC2D2A-Related Disorders (CC2D2A)
    No disease-causing variants detected
    Cerebellar Ataxia, Intellectual Disability, and Dysequilibrium Syndrome 1 (VLDLR)
    No disease-causing variants detected
    Cerebral Creatine Deficiency Syndrome 1, X-Linked (SLC6A8)
    No disease-causing variants detected
    Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Keratoderma (SNAP29)
    No disease-causing variants detected
    Cerebrotendinous Xanthomatosis (CYP27A1)
    No disease-causing variants detected
    Charcot-Marie-Tooth Disease, Type 4D (NDRG1)
    No disease-causing variants detected
    Charcot-Marie-Tooth Disease, Type 5 / Arts Syndrome, X-Linked (PRPS1)
    No disease-causing variants detected
    Charcot-Marie-Tooth Disease, X-Linked (GJB1)
    No disease-causing variants detected
    Chediak-Higashi Syndrome (LYST)
    No disease-causing variants detected
    Childhood-Onset Dystonia with Optic Atrophy and Basal Ganglia Abnormalities (MECR)
    No disease-causing variants detected
    Chondrodysplasia Punctata Type 1, X-Linked (ARSL)
    No disease-causing variants detected
    Choreoacanthocytosis (VPS13A)
    No disease-causing variants detected
    Choroidemia, X-Linked (CHM)
    No disease-causing variants detected
    Chromosome Analysis (Karyotype)
    Normal male karyotype
    Chronic Granulomatous Disease, CYBA-Related (CYBA)
    No disease-causing variants detected
    Chronic Granulomatous Disease, CYBB-Related, X-Linked (CYBB)
    No disease-causing variants detected
    Chronic Granulomatous Disease, NCF2-Related (NCF2)
    No disease-causing variants detected
    Citrin Deficiency (SLC25A13)
    No disease-causing variants detected
    Citrullinemia Type 1 (ASS1)
    No disease-causing variants detected
    Cobalamin F Deficiency (LMBRD1)
    No disease-causing variants detected
    Cockayne Syndrome Type A (ERCC8)
    No disease-causing variants detected
    Cockayne Syndrome Type B (ERCC6)
    No disease-causing variants detected
    Cohen Syndrome (VPS13B)
    No disease-causing variants detected
    COL11A2-Related Disorders (COL11A2)
    No disease-causing variants detected
    COL17A1-Related Disorders (COL17A1)
    No disease-causing variants detected
    Combined Malonic and Methylmalonic Aciduria (ACSF3)
    No disease-causing variants detected
    Combined Oxidative Phosphorylation Deficiency 1 (GFM1)
    No disease-causing variants detected
    Combined Oxidative Phosphorylation Deficiency 3 (TSFM)
    No disease-causing variants detected
    Combined Pituitary Hormone Deficiency 2 (PROP1)
    No disease-causing variants detected
    Combined Pituitary Hormone Deficiency 3 (LHX3)
    No disease-causing variants detected
    Combined Pituitary Hormone Deficiency, POU1F1-Related (POU1F1)
    No disease-causing variants detected
    Combined SAP Deficiency (PSAP)
    No disease-causing variants detected
    Congenital Adrenal Hyperplasia due to 11-Beta-Hydroxylase Deficiency (CYP11B1)
    No disease-causing variants detected
    Congenital Adrenal Hyperplasia due to 17-Alpha-Hydroxylase Deficiency (CYP17A1)
    No disease-causing variants detected
    Congenital Adrenal Hyperplasia due to 3-Beta-Hydroxysteroid Dehydrogenase Type II Deficiency (HSD3B2)
    No disease-causing variants detected
    Congenital Adrenal Hypoplasia, X-Linked (NR0B1)
    No disease-causing variants detected
    Congenital Adrenal Insufficiency (CYP11A1)
    No disease-causing variants detected
    Congenital Amegakaryocytic Thrombocytopenia (MPL)
    No disease-causing variants detected
    Congenital Disorder of Glycosylation Type 1a, PMM2-Related (PMM2)
    No disease-causing variants detected
    Congenital Disorder of Glycosylation Type 1b (MPI)
    No disease-causing variants detected
    Congenital Disorder of Glycosylation Type Ik (ALG1)
    No disease-causing variants detected
    Congenital Disorder of Glycosylation Type Iv (NGLY1)
    No disease-causing variants detected
    Congenital Disorder of Glycosylation, Type Ic (ALG6)
    No disease-causing variants detected
    Congenital Dyserythropoietic Anemia Type II (SEC23B)
    No disease-causing variants detected
    Congenital Hydrocephalus-1 (CCDC88C)
    No disease-causing variants detected
    Congenital Hypothyroidism, TSHB-Related (TSHB)
    No disease-causing variants detected
    Congenital Insensitivity to Pain with Anhidrosis (NTRK1)
    No disease-causing variants detected
    Congenital Myasthenic Syndrome (CHRNE)
    No disease-causing variants detected
    Congenital Myasthenic Syndrome (RAPSN)
    No disease-causing variants detected
    Congenital Myasthenic Syndrome, CHAT-Related (CHAT)
    No disease-causing variants detected
    Congenital Neutropenia (HAX1)
    No disease-causing variants detected
    Congenital Neutropenia, VPS45-Related (VPS45)
    No disease-causing variants detected
    Congenital Secretory Chloride Diarrhea (SLC26A3)
    No disease-causing variants detected
    Corneal Dystrophy and Perceptive Deafness (SLC4A11)
    No disease-causing variants detected
    CTSC-Related Disorders (CTSC)
    No disease-causing variants detected
    CYP1B1-Related Disorders (CYP1B1)
    No disease-causing variants detected
    CYP7B1-Related Disorders (CYP7B1)
    No disease-causing variants detected
    Cystic Fibrosis and Other CFTR-Related Disorders (CFTR)
    No disease-causing variants detected
    Cystinosis (CTNS)
    No disease-causing variants detected
    Cytochrome P450 Oxidoreductase Deficiency (POR)
    No disease-causing variants detected
    D-Bifunctional Protein Deficiency (HSD17B4)
    No disease-causing variants detected
    Deafness, Autosomal Recessive 77 (LOXHD1)
    No disease-causing variants detected
    Desbuquois Dysplasia Type 1 (CANT1)
    No disease-causing variants detected
    Developmental and Epileptic Encephalopathy, CAD-Related (CAD)
    No disease-causing variants detected
    DGUOK-Related Disorders (DGUOK)
    No disease-causing variants detected
    DOK7-Related Disorders (DOK7)
    No disease-causing variants detected
    Donnai-Barrow Syndrome (LRP2)
    No disease-causing variants detected
    Dubin-Johnson Syndrome (ABCC2)
    No disease-causing variants detected
    DUOX2-Related Disorders (DUOX2)
    No disease-causing variants detected
    DYNC2H1-Related Disorders (DYNC2H1)
    No disease-causing variants detected
    Dyskeratosis Congenita Spectrum Disorders, DKC1-Related, X-Linked (DKC1)
    No disease-causing variants detected
    Dyskeratosis Congenita Spectrum Disorders, TERT-Related (TERT)
    No disease-causing variants detected
    Dyskeratosis Congenita, RTEL1-Related (RTEL1)
    No disease-causing variants detected
    Dystrophic Epidermolysis Bullosa (COL7A1)
    No disease-causing variants detected
    Dystrophinopathies, DMD-Related, X-Linked (DMD)
    No disease-causing variants detected
    Ehlers-Danlos Syndrome, Kyphoscoliotic Type (PLOD1)
    No disease-causing variants detected
    Ehlers-Danlos Syndrome, Type VIIC (ADAMTS2)
    No disease-causing variants detected
    Ellis-Van Creveld Syndrome, EVC-Related (EVC)
    No disease-causing variants detected
    Ellis-Van Creveld Syndrome, EVC2-Related (EVC2)
    No disease-causing variants detected
    Emery-Dreifuss Muscular Dystrophy, X-Linked (EMD)
    No disease-causing variants detected
    Enhanced S-Cone Syndrome (NR2E3)
    No disease-causing variants detected
    Epidermolysis Bullosa with Pyloric Atresia, ITGB4-Related (ITGB4)
    No disease-causing variants detected
    Epimerase Deficiency Galactosemia (GALE)
    No disease-causing variants detected
    ERCC2-Related Disorders (ERCC2)
    No disease-causing variants detected
    Ethylmalonic Encephalopathy (ETHE1)
    No disease-causing variants detected
    F5-Related Disorders (F5)
    No disease-causing variants detected
    Fabry Disease, X-Linked (GLA)
    No disease-causing variants detected
    Factor IX Deficiency, X-Linked (F9)
    No disease-causing variants detected
    Factor XI Deficiency (F11)
    No disease-causing variants detected
    Familial Dysautonomia (ELP1)
    No disease-causing variants detected
    Familial Hemophagocytic Lymphohistiocytosis Type 2 (PRF1)
    No disease-causing variants detected
    Familial Hemophagocytic Lymphohistiocytosis Type 3 (UNC13D)
    No disease-causing variants detected
    Familial Hemophagocytic Lymphohistiocytosis Type 4 (STX11)
    No disease-causing variants detected
    Familial Hemophagocytic Lymphohistiocytosis Type 5 (STXBP2)
    No disease-causing variants detected
    Familial Hypercholesterolemia (LDLR)
    No disease-causing variants detected
    Familial Hypercholesterolemia (LDLRAP1)
    No disease-causing variants detected
    Familial Hyperinsulinism and Other ABCC8-Related Disorders (ABCC8)
    No disease-causing variants detected
    Familial Hyperinsulinism and Other KCNJ11-Related Disorders (KCNJ11)
    No disease-causing variants detected
    Familial Mediterranean Fever (MEFV)
    No disease-causing variants detected
    Fanconi Anemia Type A (FANCA)
    No disease-causing variants detected
    Fanconi Anemia Type B, X-Linked (FANCB)
    No disease-causing variants detected
    Fanconi Anemia Type C (FANCC)
    No disease-causing variants detected
    Fanconi Anemia Type D2 (FANCD2)
    No disease-causing variants detected
    Fanconi Anemia Type E (FANCE)
    No disease-causing variants detected
    Fanconi Anemia Type I (FANCI)
    No disease-causing variants detected
    Fanconi Anemia Type L (FANCL)
    No disease-causing variants detected
    Fanconi Anemia, Type G (FANCG)
    No disease-causing variants detected
    FHL1-Related Disorders, X-Linked (FHL1)
    No disease-causing variants detected
    FKBP10-Related Disorders (FKBP10)
    No disease-causing variants detected
    FKTN-Related Disorders including Walker-Warburg Syndrome (FKTN)
    No disease-causing variants detected
    Foveal Hypoplasia, SLC38A8-Related (SLC38A8)
    No disease-causing variants detected
    FOXN1-Related Disorders (FOXN1)
    No disease-causing variants detected
    Fragile X Syndrome, X-Linked (FMR1)
    No disease-causing mutations detected; CGG repeat number within normal range
    Fraser Syndrome, FRAS1-Related (FRAS1)
    No disease-causing variants detected
    Fraser Syndrome, FREM2-Related (FREM2)
    No disease-causing variants detected
    Fraser Syndrome, GRIP1-Related (GRIP1)
    No disease-causing variants detected
    Fructose-1,6-Bisphosphatase Deficiency (FBP1)
    No disease-causing variants detected
    Fucosidosis (FUCA1)
    No disease-causing variants detected
    Fumarase Deficiency (FH)
    No disease-causing variants detected
    Galactokinase Deficiency (GALK1)
    No disease-causing variants detected
    Galactosemia, GALT-Related (GALT)
    No disease-causing variants detected
    Galactosialidosis (CTSA)
    No disease-causing variants detected
    GATM-Related Disorders (GATM)
    No disease-causing variants detected
    Gaucher Disease (GBA)
    No disease-causing variants detected
    GCH1-Related Disorders (GCH1)
    No disease-causing variants detected
    GDF5-Related Disorders (GDF5)
    No disease-causing variants detected
    Geroderma Osteodysplastica (GORAB)
    No disease-causing variants detected
    GHR-Related Disorders (GHR)
    No disease-causing variants detected
    Gitelman Syndrome (SLC12A3)
    No disease-causing variants detected
    GJB2-Related DFNB1 Nonsyndromic Hearing Loss and Deafness (GJB2)
    No disease-causing variants detected
    Glucose-6-Phosphate Dehydrogenase Deficiency, X-Linked (G6PD)
    No disease-causing variants detected
    Glutaric Acidemia Type 1 (GCDH)
    No disease-causing variants detected
    Glutaric Acidemia Type IIB (ETFB)
    No disease-causing variants detected
    Glutaric Acidemia, Type IIa (ETFA)
    No disease-causing variants detected
    Glutaric Acidemia, Type IIc (ETFDH)
    No disease-causing variants detected
    Glutathione Synthetase Deficiency (GSS)
    No disease-causing variants detected
    Glycine Encephalopathy, AMT-Related (AMT)
    No disease-causing variants detected
    Glycine Encephalopathy, GLDC-Related (GLDC)
    No disease-causing variants detected
    Glycogen Storage Disease Type Ia (G6PC)
    No disease-causing variants detected
    Glycogen Storage Disease Type Ib (SLC37A4)
    No disease-causing variants detected
    Glycogen Storage Disease Type III (AGL)
    No disease-causing variants detected
    Glycogen Storage Disease Type IXb (PHKB)
    No disease-causing variants detected
    Glycogen Storage Disease Type IXc (PHKG2)
    No disease-causing variants detected
    Glycogen Storage Disease Type V (PYGM)
    No disease-causing variants detected
    Glycogen Storage Disease, Type IV also known as Adult Polyglucosan Body Disease (GBE1)
    No disease-causing variants detected
    Glycogen Storage Disease, Type VII (PFKM)
    No disease-causing variants detected
    GM3 Synthase Deficiency (ST3GAL5)
    No disease-causing variants detected
    GRACILE Syndrome (BCS1L)
    No disease-causing variants detected
    Guanidinoacetate Methyltransferase Deficiency also known as Cerebral Creatine Deficiency Syndrome 2 (GAMT)
    No disease-causing variants detected
    GUCY2D-Related Disorders (GUCY2D)
    No disease-causing variants detected
    HCFC1-Related Disorders, X-Linked (HCFC1)
    No disease-causing variants detected
    Heme Oxygenase 1 Deficiency (HMOX1)
    No disease-causing variants detected
    Hemochromatosis, Type 3 (TFR2)
    No disease-causing variants detected
    Hemolytic Anemia, CD59-Mediated (CD59)
    No disease-causing variants detected
    Hereditary Fructose Intolerance (ALDOB)
    No disease-causing variants detected
    Hereditary Hemochromatosis (HJV)
    No disease-causing variants detected
    Hereditary Hemochromatosis Type 1 (HFE)
    No disease-causing variants detected
    Hereditary Hemochromatosis Type 2, HAMP-Related (HAMP)
    No disease-causing variants detected
    Hereditary Spastic Paraparesis 49 (TECPR2)
    No disease-causing variants detected
    Hermansky-Pudlak Syndrome Type 4 (HPS4)
    No disease-causing variants detected
    Hermansky-Pudlak Syndrome Type 5 (HPS5)
    No disease-causing variants detected
    Hermansky-Pudlak Syndrome Type 6 (HPS6)
    No disease-causing variants detected
    Hermansky-Pudlak Syndrome Type 8 (BLOC1S3)
    No disease-causing variants detected
    Hermansky-Pudlak Syndrome Type 9 (BLOC1S6)
    No disease-causing variants detected
    Hermansky-Pudlak Syndrome, Type 1 (HPS1)
    No disease-causing variants detected
    Hermansky-Pudlak Syndrome, Type 3 (HPS3)
    No disease-causing variants detected
    Holocarboxylase Synthetase Deficiency (HLCS)
    No disease-causing variants detected
    Homocystinuria (CBS)
    No disease-causing variants detected
    Homocystinuria due to Cobalamin G Deficiency (MTR)
    No disease-causing variants detected
    Homocystinuria due to MTHFR Deficiency (MTHFR)
    No disease-causing variants detected
    Homocystinuria, Cobalamin E Type (MTRR)
    No disease-causing variants detected
    HPRT1-Related Disorders, X-Linked (HPRT1)
    No disease-causing variants detected
    Hydrolethalus Syndrome (HYLS1)
    No disease-causing variants detected
    Hyper-IgM Immunodeficiency, CD40-Related (CD40)
    No disease-causing variants detected
    Hyper-IgM Immunodeficiency, X-Linked (CD40LG)
    No disease-causing variants detected
    Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome (SLC25A15)
    No disease-causing variants detected
    Hyperphosphatemic Familial Tumoral Calcinosis, GALNT3-Related (GALNT3)
    No disease-causing variants detected
    Hypohidrotic Ectodermal Dysplasia, X-Linked (EDA)
    No disease-causing variants detected
    Hypomyelinating Leukodystrophy-12 (VPS11)
    No disease-causing variants detected
    Hypophosphatasia, Autosomal Recessive (ALPL)
    No disease-causing variants detected
    Ichthyosis Prematurity Syndrome (SLC27A4)
    No disease-causing variants detected
    IGHMBP2-Related Disorders (IGHMBP2)
    No disease-causing variants detected
    IKBKB-Related Disorders (IKBKB)
    No disease-causing variants detected
    Imerslund-Gr Sbeck Syndrome (AMN)
    No disease-causing variants detected
    Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 (DNMT3B)
    No disease-causing variants detected
    Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 2 (ZBTB24)
    No disease-causing variants detected
    Inclusion Body Myopathy 2 (GNE)
    No disease-causing variants detected
    Isolated Ectopia Lentis (ADAMTSL4)
    No disease-causing variants detected
    Isovaleric Acidemia (IVD)
    No disease-causing variants detected
    ITGB3-Related Disorders (ITGB3)
    No disease-causing variants detected
    Johanson-Blizzard Syndrome (UBR1)
    No disease-causing variants detected
    Joubert Syndrome 2 (TMEM216)
    No disease-causing variants detected
    Joubert Syndrome 7 also known as Meckel Syndrome 5 (RPGRIP1L)
    No disease-causing variants detected
    Junctional Epidermolysis Bullosa (LAMA3)
    No disease-causing variants detected
    Junctional Epidermolysis Bullosa (LAMB3)
    No disease-causing variants detected
    Junctional Epidermolysis Bullosa (LAMC2)
    No disease-causing variants detected
    Junctional Epidermolysis Bullosa with Pyloric Atresia, ITGA6-Related (ITGA6)
    No disease-causing variants detected
    Juvenile Retinoschisis, X-Linked (RS1)
    No disease-causing variants detected
    Krabbe Disease (GALC)
    No disease-causing variants detected
    L1 Syndrome, X-Linked (L1CAM)
    No disease-causing variants detected
    Leber Congenital Amaurosis (AIPL1)
    No disease-causing variants detected
    Leber Congenital Amaurosis 10 and Other CEP290-Related Ciliopathies (CEP290)
    No disease-causing variants detected
    Leber Congenital Amaurosis 13 (RDH12)
    No disease-causing variants detected
    Leber Congenital Amaurosis 2 also known as Retinitis Pigmentosa 20 (RPE65)
    No disease-causing variants detected
    Leber Congenital Amaurosis 5 (LCA5)
    No disease-causing variants detected
    Leber Congenital Amaurosis 8 also known as Retinitis Pigmentosa 12 (CRB1)
    No disease-causing variants detected
    Leigh Syndrome, French-Canadian Type (LRPPRC)
    No disease-causing variants detected
    Lethal Congenital Contracture Syndrome 1 (GLE1)
    No disease-causing variants detected
    Leukoencephalopathy with Vanishing White Matter, EIF2B1-Related (EIF2B1)
    No disease-causing variants detected
    Leukoencephalopathy with Vanishing White Matter, EIF2B2-Related (EIF2B2)
    No disease-causing variants detected
    Leukoencephalopathy with Vanishing White Matter, EIF2B3-Related (EIF2B3)
    No disease-causing variants detected
    Leukoencephalopathy with Vanishing White Matter, EIF2B4-Related (EIF2B4)
    No disease-causing variants detected
    LIG4 Syndrome (LIG4)
    No disease-causing variants detected
    Limb-Girdle Muscular Dystrophy Type 2A also known as Calpainopathy (CAPN3)
    No disease-causing variants detected
    Limb-Girdle Muscular Dystrophy Type 2B also known as Dysferlinopathy (DYSF)
    No disease-causing variants detected
    Limb-Girdle Muscular Dystrophy Type 2C also known as Gamma-Sarcoglycanopathy (SGCG)
    No disease-causing variants detected
    Limb-Girdle Muscular Dystrophy Type 2D also known as Alpha-Sarcoglycanopathy (SGCA)
    No disease-causing variants detected
    Limb-Girdle Muscular Dystrophy Type 2E also known as Beta-Sarcoglycanopathy (SGCB)
    No disease-causing variants detected
    Limb-Girdle Muscular Dystrophy Type 2F also known as Delta-Sarcoglycanopathy (SGCD)
    No disease-causing variants detected
    Limb-Girdle Muscular Dystrophy Type 2I (FKRP)
    No disease-causing variants detected
    Lipoid Adrenal Hyperplasia (STAR)
    No disease-causing variants detected
    Lipoprotein Lipase Deficiency (LPL)
    No disease-causing variants detected
    Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (HADHA)
    No disease-causing variants detected
    LRAT-Related Disorders (LRAT)
    No disease-causing variants detected
    Lysinuric Protein Intolerance (SLC7A7)
    No disease-causing variants detected
    Lysosomal Acid Lipase Deficiency including Wolman Disease and Cholesteryl Ester Storage Disease (LIPA)
    No disease-causing variants detected
    Major Histocompatibility Complex Class II Deficiency also known as Bare Lymphocyte Syndrome Type II (CIITA)
    No disease-causing variants detected
    Malonyl-CoA Decarboxylase Deficiency (MLYCD)
    No disease-causing variants detected
    Maple Syrup Urine Disease Type 1A (BCKDHA)
    No disease-causing variants detected
    Maple Syrup Urine Disease Type 1B (BCKDHB)
    No disease-causing variants detected
    Maple Syrup Urine Disease Type 2 (DBT)
    No disease-causing variants detected
    Maple Syrup Urine Disease Type 3 also known as Dihyrolipoamide Dehydrogenase Deficiency (DLD)
    No disease-causing variants detected
    MECP2-Related Disorders, X-Linked (MECP2)
    No disease-causing variants detected
    Medium Chain Acyl-CoA Dehydrogenase Deficiency (ACADM)
    No disease-causing variants detected
    MEDNIK Syndrome (AP1S1)
    No disease-causing variants detected
    Megalencephalic Leukoencephalopathy With Subcortical Cysts Type 1 (MLC1)
    No disease-causing variants detected
    Menkes Disease and Other ATP7A-Related Disorders, X-Linked (ATP7A)
    No disease-causing variants detected
    Merosin-Deficient Muscular Dystrophy (LAMA2)
    No disease-causing variants detected
    Metabolic Crises with Rhabdomyolysis, Cardiac Arrhythmias and Neurodegeneration (TANGO2)
    No disease-causing variants detected
    Metachromatic Leukodystrophy (ARSA)
    No disease-causing variants detected
    Methylmalonic Acidemia (MMAA)
    No disease-causing variants detected
    Methylmalonic Acidemia (MMAB)
    No disease-causing variants detected
    Methylmalonic Acidemia (MUT)
    No disease-causing variants detected
    Methylmalonic Acidemia, MCEE-Related (MCEE)
    No disease-causing variants detected
    Methylmalonic Aciduria and Homocystinuria, Cobalamin C Type (MMACHC)
    No disease-causing variants detected
    Methylmalonic Aciduria and Homocystinuria, Cobalamin D Type (MMADHC)
    No disease-causing variants detected
    Microcephalic Osteodysplastic Primordial Dwarfism Type II (PCNT)
    No disease-causing variants detected
    Microphthalmia and Anophthalmia (VSX2)
    No disease-causing variants detected
    Mitochondrial Complex I Deficiency (ACAD9)
    No disease-causing variants detected
    Mitochondrial Complex I Deficiency 1 (NDUFS4)
    No disease-causing variants detected
    Mitochondrial Complex I Deficiency 10 (NDUFAF2)
    No disease-causing variants detected
    Mitochondrial Complex I Deficiency 12 (PET100)
    No disease-causing variants detected
    Mitochondrial Complex I Deficiency 16 (NDUFAF5)
    No disease-causing variants detected
    Mitochondrial Complex I Deficiency 19 (FOXRED1)
    No disease-causing variants detected
    Mitochondrial Complex I Deficiency 3 (NDUFS7)
    No disease-causing variants detected
    Mitochondrial Complex I Deficiency 4 (NDUFV1)
    No disease-causing variants detected
    Mitochondrial Complex I Deficiency 6 (COX15)
    No disease-causing variants detected
    Mitochondrial Complex I Deficiency, NDUFS6-Related (NDUFS6)
    No disease-causing variants detected
    Mitochondrial DNA Depletion Syndrome 6 also known as Navajo Neurohepatopathy (MPV17)
    No disease-causing variants detected
    Mitochondrial DNA Depletion Syndrome-2 (TK2)
    No disease-causing variants detected
    Mitochondrial Myopathy and Sideroblastic Anemia 1 (PUS1)
    No disease-causing variants detected
    Mitochondrial Neurogastrointestinal Encephalopathy Disease (TYMP)
    No disease-causing variants detected
    Mitochondrial Trifunctional Protein Deficiency, HADHB-Related (HADHB)
    No disease-causing variants detected
    MKKS-Related Disorders (MKKS)
    No disease-causing variants detected
    MKS1-Related Disorders, including Bardet-Biedl Syndrome 13, Joubert Syndrome 28, and Meckel Syndrome 1 (MKS1)
    No disease-causing variants detected
    Molybdenum Cofactor Deficiency, MOCS1-Related (MOCS1)
    No disease-causing variants detected
    Molybdenum Cofactor Deficiency, MOCS2A-Related (MOCS2A)
    No disease-causing variants detected
    Molybdenum Cofactor Deficiency, MOCS2B-Related (MOCS2B)
    No disease-causing variants detected
    Mucolipidosis II and IIIA (GNPTAB)
    No disease-causing variants detected
    Mucolipidosis III Gamma (GNPTG)
    No disease-causing variants detected
    Mucolipidosis Type IV (MCOLN1)
    No disease-causing variants detected
    Mucopolysaccharidosis Type I also known as Hurler Syndrome (IDUA)
    No disease-causing variants detected
    Mucopolysaccharidosis Type II also known as Hunter Syndrome, X-Linked (IDS)
    No disease-causing variants detected
    Mucopolysaccharidosis Type IIIA also known as Sanfilippo A Syndrome (SGSH)
    No disease-causing variants detected
    Mucopolysaccharidosis Type IIIB also known as Sanfilippo B Syndrome (NAGLU)
    No disease-causing variants detected
    Mucopolysaccharidosis Type IIIC also known as Sanfilippo C Syndrome (HGSNAT)
    No disease-causing variants detected
    Mucopolysaccharidosis Type IIID (GNS)
    No disease-causing variants detected
    Mucopolysaccharidosis Type IVA (GALNS)
    No disease-causing variants detected
    Mucopolysaccharidosis Type IVb also known as GM1 Gangliosidosis (GLB1)
    No disease-causing variants detected
    Mucopolysaccharidosis Type VI (ARSB)
    No disease-causing variants detected
    Mucopolysaccharidosis Type VII (GUSB)
    No disease-causing variants detected
    Mucopolysaccharidosistype IX (HYAL1)
    No disease-causing variants detected
    Mulibrey Nanism (TRIM37)
    No disease-causing variants detected
    Multiple Pterygium Syndrome (CHRNG)
    No disease-causing variants detected
    Multiple Sulphatase Deficiency (SUMF1)
    No disease-causing variants detected
    Muscle-Eye-Brain Disease (POMGNT1)
    No disease-causing variants detected
    Muscular Dystrophy-Dystroglycanopathy, LARGE1-Related (LARGE1)
    No disease-causing variants detected
    Muscular Dystrophy-Dystroglycanopathy, POMT1-Related (POMT1)
    No disease-causing variants detected
    Muscular Dystrophy-Dystroglycanopathy, POMT2-Related (POMT2)
    No disease-causing variants detected
    Muscular Dystrophy-Dystroglycanopathy, RXYLT1-Related (RXYLT1)
    No disease-causing variants detected
    MUSK-Related Disorders (MUSK)
    No disease-causing variants detected
    MVK-Related Disorders (MVK)
    No disease-causing variants detected
    Myotonia Congenita (CLCN1)
    No disease-causing variants detected
    Myotubular Myopathy, X-Linked (MTM1)
    No disease-causing variants detected
    N-Acetylglutamate Synthase Deficiency (NAGS)
    No disease-causing variants detected
    Nemaline Myopathy 2 (NEB)
    No disease-causing variants detected
    Nephrogenic Diabetes Insipidus, Type II (AQP2)
    No disease-causing variants detected
    Nephronophthisis, INVS-Related (INVS)
    No disease-causing variants detected
    Nephronophthisis, NPHP1-Related (NPHP1)
    No disease-causing variants detected
    Nephrotic Syndrome, NPHS1-Related also known as Congenital Finnish Nephrosis (NPHS1)
    No disease-causing variants detected
    Nephrotic Syndrome, NPHS2-Related also known as Steroid-Resistant Nephrotic Syndrome (NPHS2)
    No disease-causing variants detected
    Neuronal Ceroid Lipofuscinosis Type 10 (CTSD)
    No disease-causing variants detected
    Neuronal Ceroid-Lipofuscinosis, CLN3-Related (CLN3)
    No disease-causing variants detected
    Neuronal Ceroid-Lipofuscinosis, CLN5-Related (CLN5)
    No disease-causing variants detected
    Neuronal Ceroid-Lipofuscinosis, CLN6-Related (CLN6)
    No disease-causing variants detected
    Neuronal Ceroid-Lipofuscinosis, CLN8-Related also known as Northern Epilepsy (CLN8)
    No disease-causing variants detected
    Neuronal Ceroid-Lipofuscinosis, MFSD8-Related (MFSD8)
    No disease-causing variants detected
    Neuronal Ceroid-Lipofuscinosis, PPT1-Related (PPT1)
    No disease-causing variants detected
    Neuronal Ceroid-Lipofuscinosis, TPP1-Related (TPP1)
    No disease-causing variants detected
    Niemann-Pick Disease Type A/B (SMPD1)
    No disease-causing variants detected
    Niemann-Pick Disease Type C, NPC1-Related (NPC1)
    No disease-causing variants detected
    Niemann-Pick Disease Type C, NPC2-Related (NPC2)
    No disease-causing variants detected
    Nijmegen Breakage Syndrome (NBN)
    No disease-causing variants detected
    Nonsyndromic Deafness, MYO15A-Related (MYO15A)
    No disease-causing variants detected
    Nonsyndromic Deafness, OTOA-Related (OTOA)
    No disease-causing variants detected
    Nonsyndromic Deafness, OTOF-Related (OTOF)
    No disease-causing variants detected
    Nonsyndromic Deafness, SYNE4-Related (SYNE4)
    No disease-causing variants detected
    Nonsyndromic Deafness, TMC1-Related (TMC1)
    No disease-causing variants detected
    Nonsyndromic Deafness, TMPRSS3-Related (TMPRSS3)
    No disease-causing variants detected
    Nonsyndromic Intellectual Disability, CC2D1A-Related (CC2D1A)
    No disease-causing variants detected
    NSMCE3 Deficiency (NSMCE3)
    No disease-causing variants detected
    OCRL-Related Disorders, X-Linked (OCRL)
    No disease-causing variants detected
    Oculocutaneous Albinism Type 2 (OCA2)
    No disease-causing variants detected
    Oculocutaneous Albinism Type 3 (TYRP1)
    No disease-causing variants detected
    Oculocutaneous Albinism Type 4 (SLC45A2)
    No disease-causing variants detected
    Oculocutaneous Albinism Types 1A and 1B (TYR)
    No disease-causing variants detected
    Odonto-Onycho-Dermal Dysplasia also known as Schopf-Schulz-Passarge Syndrome (WNT10A)
    No disease-causing variants detected
    Omenn Syndrome and Severe Combined Immunodeficiency, Athabaskan-Type (DCLRE1C)
    No disease-causing variants detected
    Omenn Syndrome, RAG2-Related (RAG2)
    No disease-causing variants detected
    Opitz GBBB Syndrome, MID1-Related, X-Linked (MID1)
    No disease-causing variants detected
    Ornithine Aminotransferase Deficiency (OAT)
    No disease-causing variants detected
    Ornithine Transcarbamylase Deficiency, X-Linked (OTC)
    No disease-causing variants detected
    Osteochondrodysplasias, Sulfate Transporter-Related (SLC26A2)
    No disease-causing variants detected
    Osteogenesis Imperfecta, BMP1-Related (BMP1)
    No disease-causing variants detected
    Osteogenesis Imperfecta, CRTAP-Related (CRTAP)
    No disease-causing variants detected
    Osteogenesis Imperfecta, P3H1-Related (P3H1)
    No disease-causing variants detected
    Osteopetrosis Type 1 (TCIRG1)
    No disease-causing variants detected
    OSTM1 Deficiency Associated Osteopetrosis (OSTM1)
    No disease-causing variants detected
    Pantothenate Kinase-Associated Neurodegeneration (PANK2)
    No disease-causing variants detected
    Parkinson Disease 15 (FBXO7)
    No disease-causing variants detected
    Pendred Syndrome (SLC26A4)
    No disease-causing variants detected
    Peroxisome Biogenesis Disorder, Type 3 (PEX12)
    No disease-causing variants detected
    PEX5-Related Disorders (PEX5)
    No disease-causing variants detected
    PGM3-Gongenital Disorder of Glycosylation (PGM3)
    No disease-causing variants detected
    Phenylalanine Hydroxylase Deficiency also known as Phenylketonuria (PAH)
    No disease-causing variants detected
    PIGN-Congenital Disorder of Glycosylation (PIGN)
    No disease-causing variants detected
    PJVK-Related Disorders (PJVK)
    No disease-causing variants detected
    PLA2G6-Related Disorders (PLA2G6)
    No disease-causing variants detected
    PLEKHG5-Related Disorders (PLEKHG5)
    No disease-causing variants detected
    PLP1-Related Disorders, X-Linked (PLP1)
    No disease-causing variants detected
    POLG-Related Disorders (POLG)
    No disease-causing variants detected
    Polycystic Kidney Disease, Autosomal Recessive (PKHD1)
    No disease-causing variants detected
    Polyglandular Autoimmune Syndrome Type 1 (AIRE)
    No disease-causing variants detected
    Polymicrogyria (ADGRG1)
    No disease-causing variants detected
    Pompe Disease also known as Glycogen Storage Disease Type II (GAA)
    No disease-causing variants detected
    Pontocerebellar Hypoplasia Type 1A (VRK1)
    No disease-causing variants detected
    Pontocerebellar Hypoplasia Type 1B (EXOSC3)
    No disease-causing variants detected
    Pontocerebellar Hypoplasia Type 6 (RARS2)
    No disease-causing variants detected
    Pontocerebellar Hypoplasia, TSEN54-Related (TSEN54)
    No disease-causing variants detected
    Postnatal Progressive Microcephaly also known as Infantile Cerebral and Cerebellar Atrophy (MED17)
    No disease-causing variants detected
    Primary Carnitine Deficiency (SLC22A5)
    No disease-causing variants detected
    Primary Ciliary Dyskinesia, CCDC103-Related (CCDC103)
    No disease-causing variants detected
    Primary Ciliary Dyskinesia, CCDC39-Related (CCDC39)
    No disease-causing variants detected
    Primary Ciliary Dyskinesia, DNAH11-Related (DNAH11)
    No disease-causing variants detected
    Primary Ciliary Dyskinesia, DNAH5-Related (DNAH5)
    No disease-causing variants detected
    Primary Ciliary Dyskinesia, DNAI1-Related (DNAI1)
    No disease-causing variants detected
    Primary Ciliary Dyskinesia, DNAI2-Related (DNAI2)
    No disease-causing variants detected
    Primary Hyperoxaluria Type 1 (AGXT)
    No disease-causing variants detected
    Primary Hyperoxaluria Type 2 (GRHPR)
    No disease-causing variants detected
    Primary Hyperoxaluria, Type 3 (HOGA1)
    No disease-causing variants detected
    Primary Microcephaly, MCPH1-Related (MCPH1)
    No disease-causing variants detected
    Progressive Cerebello-Cerebral Atrophy (SEPSECS)
    No disease-causing variants detected
    Progressive Early-Onset Encepahlopathy with Brain Atrophy and Thin Corpus Callosum (TBCD)
    No disease-causing variants detected
    Progressive Familial Intrahepatic Cholestasis 3 (ABCB4)
    No disease-causing variants detected
    Progressive Familial Intrahepatic Cholestasis Type 2 (ABCB11)
    No disease-causing variants detected
    Progressive Pseudorheumatoid Dysplasia (WISP3)
    No disease-causing variants detected
    Prolidase Deficiency (PEPD)
    No disease-causing variants detected
    Propionic Acidemia, PCCA-Related (PCCA)
    No disease-causing variants detected
    Propionic Acidemia, PCCB-Related (PCCB)
    No disease-causing variants detected
    Protein-Losing Enteropathy (DGAT1)
    No disease-causing variants detected
    Prothrombin-Related Thrombophilia (F2)
    No disease-causing variants detected
    Pycnodysostosis (CTSK)
    No disease-causing variants detected
    Pyridoxal 5'-Phosphate-Dependent Epilepsy (PNPO)
    No disease-causing variants detected
    Pyridoxine-Dependent Epilepsy, ALDH7A1-Related (ALDH7A1)
    No disease-causing variants detected
    Pyruvate Carboxylase Deficiency (PC)
    No disease-causing variants detected
    Pyruvate Dehydrogenase E1-Alpha Deficiency, X-Linked (PDHA1)
    No disease-causing variants detected
    Pyruvate Dehydrogenase E1-Beta Deficiency (PDHB)
    No disease-causing variants detected
    Refsum Disease (PHYH)
    No disease-causing variants detected
    Renal Tubular Acidosis and Deafness (ATP6V1B1)
    No disease-causing variants detected
    Retinitis Pigmentosa 2, X-Linked (RP2)
    No disease-causing variants detected
    Retinitis Pigmentosa 25 (EYS)
    No disease-causing variants detected
    Retinitis Pigmentosa 26 (CERKL)
    No disease-causing variants detected
    Retinitis Pigmentosa 28 (FAM161A)
    No disease-causing variants detected
    Retinitis Pigmentosa 36 (PRCD)
    No disease-causing variants detected
    Retinitis Pigmentosa 59 (DHDDS)
    No disease-causing variants detected
    Retinitis Pigmentosa 62 (MAK)
    No disease-causing variants detected
    Rhizomelic Chondrodysplasia Punctata Type 1 (PEX7)
    No disease-causing variants detected
    Rhizomelic Chondrodysplasia Punctata Type 2 (GNPAT)
    No disease-causing variants detected
    Rhizomelic Chondrodysplasia Punctata Type 3 (AGPS)
    No disease-causing variants detected
    RLBP1-Related Disorders (RLBP1)
    No disease-causing variants detected
    Roberts Syndrome (ESCO2)
    No disease-causing variants detected
    RYR1-Related Disorders (RYR1)
    No disease-causing variants detected
    Salla Disease (SLC17A5)
    No disease-causing variants detected
    SAMD9-Related Disorders (SAMD9)
    No disease-causing variants detected
    Sandhoff Disease (HEXB)
    No disease-causing variants detected
    Schimke Immunoosseous Dysplasia (SMARCAL1)
    No disease-causing variants detected
    Seckel Syndrome, CEP152-Related (CEP152)
    No disease-causing variants detected
    Sepiapterin Reductase Deficiency (SPR)
    No disease-causing variants detected
    Severe Combined Immunodeficiency due to CD3-Delta Deficiency (CD3D)
    No disease-causing variants detected
    Severe Combined Immunodeficiency due to CD3-Epsilon Deficiency (CD3E)
    No disease-causing variants detected
    Severe Combined Immunodeficiency due to CD45 Deficiency (PTPRC)
    No disease-causing variants detected
    Severe Combined Immunodeficiency due to IL7R-Alpha Deficiency (IL7R)
    No disease-causing variants detected
    Severe Combined Immunodeficiency due to JAK3 Deficiency (JAK3)
    No disease-causing variants detected
    Severe Combined Immunodeficiency due to RAG1 Deficiency (RAG1)
    No disease-causing variants detected
    Severe Combined Immunodeficiency, X-Linked (IL2RG)
    No disease-causing variants detected
    Severe Congenital Neutropenia due to G6PC3 Deficiency (G6PC3)
    No disease-causing variants detected
    Sialidosis (NEU1)
    No disease-causing variants detected
    Sjogren-Larsson Syndrome (ALDH3A2)
    No disease-causing variants detected
    Smith-Lemli-Opitz Syndrome (DHCR7)
    No disease-causing variants detected
    Spastic Ataxia of Charlevoix-Saguenay, Autosomal Recessive (SACS)
    No disease-causing variants detected
    Spastic Paraplegia, Type 15 (ZFYVE26)
    No disease-causing variants detected
    Spastic Tetraplegia, Thin Corpus Callosum, and Progressive Microcephaly (SLC1A4)
    No disease-causing variants detected
    SPG11-Related Disorders (SPG11)
    No disease-causing variants detected
    Spinal Muscular Atrophy (SMN1)
    No disease-causing mutations detected (2 copies detected)
    Spinocerebellar Ataxia, ANO10-Related (ANO10)
    No disease-causing variants detected
    Spondylocostal Dysostosis, DLL3-Related (DLL3)
    No disease-causing variants detected
    Spondylothoracic Dysostosis (MESP2)
    No disease-causing variants detected
    Steel Syndrome (COL27A1)
    No disease-causing variants detected
    Steroid 5-Alpha-Reductase Deficiency (SRD5A2)
    No disease-causing variants detected
    Stuve-Wiedemann Syndrome (LIFR)
    No disease-causing variants detected
    Sulfite Oxidase Deficiency (SUOX)
    No disease-causing variants detected
    SURF1-Related Disorders (SURF1)
    No disease-causing variants detected
    Tay-Sachs Disease also known as Hexosaminidase A Deficiency (HEXA)
    No disease-causing variants detected
    TBCE-Related Disorders (TBCE)
    No disease-causing variants detected
    TGM1-Related Autosomal Recessive Congenital Ichthyosis (TGM1)
    No disease-causing variants detected
    Thiamine-Responsive Megaloblastic Anemia (SLC19A2)
    No disease-causing variants detected
    Thyroid Dyshormonogenesis, SLC5A5-Related (SLC5A5)
    No disease-causing variants detected
    Thyroid Dyshormonogenesis, TG-Related (TG)
    No disease-causing variants detected
    Thyroid Dyshormonogenesis, TPO-Related (TPO)
    No disease-causing variants detected
    TMEM67-Related Disorders (TMEM67)
    No disease-causing variants detected
    Transcobalamin II Deficiency (TCN2)
    No disease-causing variants detected
    TREX1-Related Disorders (TREX1)
    No disease-causing variants detected
    Trichohepatoenteric Syndrome, SKIC2-Related (SKIC2)
    No disease-causing variants detected
    Trichohepatoenteric Syndrome, TTC37-Related (TTC37)
    No disease-causing variants detected
    TRIM32-Related Disorders (TRIM32)
    No disease-causing variants detected
    Trimethylaminuria (FMO3)
    No disease-causing variants detected
    Triple A Syndrome (AAAS)
    No disease-causing variants detected
    TSHR-Related Disorders (TSHR)
    No disease-causing variants detected
    TULP1-Related Disorders (TULP1)
    No disease-causing variants detected
    Tyrosine Hydroxylase Deficiency (TH)
    No disease-causing variants detected
    Tyrosinemia Type 1 (FAH)
    No disease-causing variants detected
    Tyrosinemia Type III (HPD)
    No disease-causing variants detected
    Tyrosinemia, Type II (TAT)
    No disease-causing variants detected
    Usher Syndrome Type IB (MYO7A)
    No disease-causing variants detected
    Usher Syndrome Type IC (USH1C)
    No disease-causing variants detected
    Usher Syndrome Type ID (CDH23)
    No disease-causing variants detected
    Usher Syndrome Type IF (PCDH15)
    No disease-causing variants detected
    Usher Syndrome Type IIIA (CLRN1)
    No disease-causing variants detected
    Vanishing White Matter Disease (EIF2B5)
    No disease-causing variants detected
    Very Long Chain Acyl-CoA Dehydrogenase Deficiency (ACADVL)
    No disease-causing variants detected
    Vici Syndrome (EPG5)
    No disease-causing variants detected
    Vitamin D-Dependent Rickets Type 1A (CYP27B1)
    No disease-causing variants detected
    Vitamin D-Dependent Rickets Type 2A (VDR)
    No disease-causing variants detected
    VPS53-Related Disorders (VPS53)
    No disease-causing variants detected
    Warsaw Syndrome (DDX11)
    No disease-causing variants detected
    WAS-Related Disorders, X-Linked (WAS)
    No disease-causing variants detected
    Werner Syndrome (WRN)
    No disease-causing variants detected
    Wilson Disease (ATP7B)
    No disease-causing variants detected
    Wolcott-Rallison Syndrome (EIF2AK3)
    No disease-causing variants detected
    Woodhouse-Sakati Syndrome (DCAF17)
    No disease-causing variants detected
    Xeroderma Pigmentosum, Group A (XPA)
    No disease-causing variants detected
    Xeroderma Pigmentosum, Group C (XPC)
    No disease-causing variants detected
    Xeroderma Pigmentosum, Variant Type (POLH)
    No disease-causing variants detected
    Zellweger Spectrum Disorder, PEX13-Related (PEX13)
    No disease-causing variants detected
    Zellweger Spectrum Disorder, PEX16-Related (PEX16)
    No disease-causing variants detected
    Zellweger Spectrum Disorder, PEX2-Related (PEX2)
    No disease-causing variants detected
    Zellweger Spectrum Disorder, PEX26-Related (PEX26)
    No disease-causing variants detected
    Zellweger Spectrum Disorder, PEX6-Related (PEX6)
    No disease-causing variants detected
    Zellweger Syndrome Spectrum (PEX1)
    No disease-causing variants detected
    Zellweger Syndrome Spectrum, PEX10- Related (PEX10)
    No disease-causing variants detected
  • Medication Allergy:
    No
    Food Allergy:
    No
    Pet Allergy:
    No
    Hay Fever Allergy:
    No
    Insect Allergy:
    No
    Vaccine Allergy:
    No
    Healthy Teeth:
    Yes
    Braces:
    Yes
    Back Problems:
    No
    Bronchitis:
    No
    Chicken Pox:
    No
    Chicken Pox Age:
    Vertigo:
    No
    Eyesight Correction:
    Yes
    Near or Far Sighted:
    Nearsighted
    Skin Infection:
    No
    Gallstones:
    No
    Removed Gall Bladder:
    No
    Hernia:
    No
    Mumps:
    No
    Measles:
    No
    Measles Age:
    German Measles:
    No
    German Measles Age:
    Sinus Infection:
    Yes
    Stomach Ulcers:
    No

  • ATHLETIC

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    COUCH POTATO

    OPTIMISTIC

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    PESSIMISTIC

    ASSERTIVE

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    PASSIVE

    LEADER

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    FOLLOWER

    EASY GOING

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    CONTROLLING, RIGID

    ARTISTIC

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    MICHELANGELO WHO?

    EXTROVERT

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    INTROVERT

    Celebrity Look Alike: Will Poulter

    Vegetarian: No

    Adjectives: Disciplined, Ambitious, Trustworthy

    Fine Art Skills: Digital Design

    Technical/Mechanical Ability: Software Engineering, mechanically inclined

    Skills, Hobbies and Interests: Hiking, cycling, puzzles, software development, anything handy.

  • Carried to Term:
    Yes
    Pregnancy Complications:
    No
    Birth Weight:
    10 lbs ounces
    Childhood Health:
    Excellent
    Birth Length:
    22 inches
    Twin:
    No
    Twin Type:
    In School:
    No
    Is the donor currently enrolled in or does the donor hold an undergraduate degree?
    Yes
    Degree Earned/Working towards:
    Bachelor of Science
    Degree Status:
    Graduated
    Major:
    Computer Science
    Minor:
    None
    Is the donor currently enrolled in or does the donor hold a graduate degree?
    No
    Is the donor currently enrolled in or does the donor have any specialized training (Including Military, Police, Firefighter, EMS, Real Estate, etc.)?
    No

  • The following medical conditions apply to the donor and his BLOOD RELATIVES ONLY (grandparents, parents, aunts, uncles, cousins, brothers, sisters, nieces, nephews and children of the donor).

    If a donor answers "yes" to any high-risk question on his Medical History Questionnaire, the donor is ineligible.

    Autoimmune Diseases Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    CREST Syndrome X
    Lupus X
    Scleroderma X
    Sjogren's Syndrome X
    Blood Diseases Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Anemia X
    Fanconi Anemia X
    Hemophilia X
    Immunodeficiency X
    Leukemia X
    Sickle Cell X
    Thalassemia X
    Von Willebrand's disease X
    Cancer Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Cancer (Breast) X
    Cancer (Colon) X
    Cancer (Leukemia) X
    Cancer (Lung) X
    Cancer (Other) X
    Cancer (Skin) X
    Lymphoma X
    Melanoma X
    Prostate X
    Tumor X
    Cardio Vascular Diseases Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Congenital Heart Disease X
    Heart Attack X
    Heart Disease X
    High Blood Pressure X
    High Cholesterol/Triglycerides X
    Stroke X
    Cardio Vascular (Other) X
    Congenital Malformations Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Deviated Septum X
    Malformations (Cleft Lip) X
    Malformations (Cleft Palate) X
    Malformations (Club Foot) X
    Malformations (Hypospadias) X
    Malformations (Other) X
    Malformations (Polydactyly) X
    Malformations (Syndactyly) X
    Undescended Testicles X
    Gastro-Intestinal Diseases Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Gallstones X
    GI (Crohn's) X
    GI (Diverticulitis) X
    GI (Other) X
    GI (Pyloric Stenosis) X
    GI (Ulcerative Colitis) X
    GI (Ulcers) X
    Hemochromatosis X
    Hepatitis X
    Kidney Diseases Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Adrenal Hyperplasia X
    Born with 1 kidney X
    Kidney (Other) X
    Kidney disease or urinary tract disorder X
    Kidney Disorder X
    Polycystic Kidney Disease X
    Progressive Kidney Disease X
    Mental Health Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Anxiety disorder X
    Mental (Depression) X
    Mental (Manic Depressive) X
    Mental (Schizophrenia) X
    Mental Retardation X
    Obsessive-compulsive disorder X
    Metabolic/Endrocrine Dis. Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Diabetes (Insulin Dependent) X
    Diabetes (Non-Insulin Dependent) X
    Galactosemia X
    Gaucher's disease X
    Goiter X
    Hypoglycemia X
    Maple Syrup disease X
    PKU or Inherited Metabolic Disorder X
    Tay Sachs X
    Thyroid Disorder X
    Muscular/Bones/Joint Disease Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Achondroplasia (Dwarfism) X
    Arthritis (Other) X
    Congenital Hip Disease X
    Gout X
    Loss of Muscle Coordination X
    Marfan's Disease X
    Muscular Dystrophy X
    Osteoarthritis X
    Osteoporosis X
    Rheumatoid Arthritis X
    Scoliosis X
    Spinal Muscular Atrophy X
    Neurological Diseases Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Learning Disorder: ADD, ADHD, Dyslexia X
    Autism/ Asperger X
    Canavan's disease X
    Cerebral Palsy X
    Dementia X
    Disorders of the spinal cord X
    Dyslexia X
    Familial dysautonomia X
    Lesch-Nyhan Syndrome X
    Migraines X
    Mucolipidosis type IV X
    Neurologic (Alzheimer) X
    Neurologic (Creutzfeldt-Jakob Disease) X
    Neurologic (Epilepsy) X
    Neurologic (Guillain Barre) X
    Neurologic (Huntington's) X
    Neurologic (JC Virus) X
    Neurologic (Lou Gehrig's Disease) X
    Neurologic (Multiple Sclerosis) X
    Neurologic (Neural Tube Defect) X
    Neurologic (Neurofibromatosis) X
    Neurologic (Parkinson's Disease) X
    Neurologic (Subacute Sclerosing Panencephalitis) X
    Nieman-Pick X
    Spongiform encephalopathy/prion disease X
    Tourette Syndrome X
    Other Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Alcoholism X
    Bloom syndrome X
    Cystic Fibrosis X
    Down Syndrome X
    Drug Abuse X
    Encephalitis: viral or of unknown origin X
    Fragile X X
    Klinefelter X
    Meningitis X
    Noonan or Turner Syndrome X
    Other - Early Death X
    Other - Inherited Genetic Condition X
    Other Disease/Condition X
    Premature Organ Degeneration X
    Radiation Exposure X
    SIDS X
    Toxic Chemical Exposure X
    Turner's Syndrome X
    West Nile (suspected or confirmed by lab testing) X
    Respiratory Disease Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Allergies (Drug) X
    Allergies (Food) X
    Allergies (Hay Fever) X
    Allergies (Insect) X
    Allergies (Other) X
    Allergies (Pet) X
    Asthma X
    Emphysema X
    SARS X
    Tuberculosis X
    Sight/Sound/Smell Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Cataracts X
    Deafness X
    Deafness (before age 50) X
    Ear deformity X
    Eyesight (Blindness) X
    Eyesight (Red-Green Color Blindness) X
    Eyesight (Glaucoma) X
    Eyesight (Other) X
    Eyesight (Retinoblastoma) X
    Macular degeneration X
    Skin Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Albinism X
    Eczema X
    Pigmentation disorders (including Vitiligo) X
    Psoriasis X
    Skin Disease X

  • Information displayed in this profile is provided by the donor. Blank fields are intentional and indicate that the information is not available.

    FAMILY MEMBER: Father
    Hair Color: Blonde, Medium Eyesight:
    Freckles: Few Hair Texture: Fine
    Health Status: Good Skin Tone: Medium Dominant Hand:
    Year of Birth: 1976 Cause of Death: Hair Loss: Receding
    Height: 5'10" (177.8 cm) Age at Death: Body Hair: Straight
    Weight: 215 lbs. (97 kg) Occupation: Technical Architect Eye Color: Blue/Green
    Half Siblings: No Education: College Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has dimples and corrected vision. Family oriented. Great father figure. Incredibly supportive of his children’s endeavors. Enjoys hiking, cycling, and working with his hands.
    FAMILY MEMBER: Mother
    Hair Color: Brown, Medium Eyesight:
    Freckles: None Hair Texture: Thick
    Health Status: Good Skin Tone: Olive Dominant Hand:
    Year of Birth: 1977 Cause of Death: Hair Loss:
    Height: 5'06" (167.64 cm) Age at Death: Body Hair: Wavy
    Weight: 155 lbs. (70 kg) Occupation: Bank Teller Eye Color: Hazel/Green
    Half Siblings: No Education: College Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has dimples. Very outgoing and passionate. In my early life, she was a homemaker. She has always been supportive. Interests include overall health. Enjoys crafts, gardening, and homesteading.
    FAMILY MEMBER: Brother
    Hair Color: Brown, Medium Eyesight:
    Freckles: Few Hair Texture: Thick
    Health Status: Good Skin Tone: Olive Dominant Hand:
    Year of Birth: 2000 Cause of Death: Hair Loss:
    Height: 5'10" (177.8 cm) Age at Death: Body Hair: Straight
    Weight: 230 lbs. (104 kg) Occupation: Maintenance, Internet Company Eye Color: Hazel/Green
    Half Siblings: No Education: High School Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has dimples. Very outgoing. Joyful. Enjoys hunting, swimming, and grilling.

  • Information displayed in this profile is provided by the donor. Blank fields are intentional and indicate that the information is not available.

    FAMILY MEMBER: Grandfather
    Hair Color: Brown, Dark Eyesight:
    Freckles: Few Hair Texture:
    Health Status: Good Skin Tone: Fair Dominant Hand:
    Year of Birth: 1954 Cause of Death: Hair Loss: Receding
    Height: 5'09" (175.26 cm) Age at Death: Body Hair: Straight
    Weight: 230 lbs. (104 kg) Occupation: Software Engineer Eye Color: Brown, Light
    Half Siblings: Education: College Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision. Worked in the Army. Enjoyed programming computers.
    FAMILY MEMBER: Grandmother
    Hair Color: Brown, Dark Eyesight:
    Freckles: Few Hair Texture: Fine
    Health Status: Good Skin Tone: Fair Dominant Hand:
    Year of Birth: 1956 Cause of Death: Hair Loss:
    Height: 5'02" (157.48 cm) Age at Death: Body Hair: Straight
    Weight: 330 lbs. (149 kg) Occupation: Hospital Receptionist Eye Color: Hazel/Blue
    Half Siblings: Education: College Body Build: Very Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Raised children while grandfather was in the Army. Enjoys arts and crafts.

  • Information displayed in this profile is provided by the donor. Blank fields are intentional and indicate that the information is not available.

    FAMILY MEMBER: Grandfather
    Hair Color: Brown, Medium Eyesight:
    Freckles: Numerous Hair Texture: Thick
    Health Status: Fair Skin Tone: Medium Dominant Hand:
    Year of Birth: 1957 Cause of Death: Hair Loss:
    Height: 5'08" (172.72 cm) Age at Death: Body Hair: Straight
    Weight: 240 lbs. (108 kg) Occupation: School Bus Mechanic Eye Color: Hazel/Green
    Half Siblings: Education: College Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has dimples. Enjoys working on vehicles and riding motorcycles.
    FAMILY MEMBER: Grandmother
    Hair Color: Brown, Dark Eyesight:
    Freckles: Numerous Hair Texture: Fine
    Health Status: Fair Skin Tone: Medium Dominant Hand:
    Year of Birth: 1958 Cause of Death: Hair Loss:
    Height: 5'07" (170.18 cm) Age at Death: Body Hair: Straight
    Weight: 130 lbs. (59 kg) Occupation: Homemaker Eye Color: Brown, Light
    Half Siblings: Education: High School Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has dimples. Enjoys arts and crafts and playing with her cats.
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