Donor Profile : Donor 5499

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Donor ID: 5499

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Meet The Donor

He plays guitar and piano, and his mother is his hero. She signed him up for a Filipino pen pal at age 8, piquing his interest in travel, other cultures, and helping those in need. Donor 5499's plan for a career in the Peace Corps fulfills his ultimate desire to help others.

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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.

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Donor's "Name": Barrett

Year of Birth: 1987

Marital Status: Single

Number of Children: 0

Religion: None

Occupation:
(last reported)
Lead Merchandiser

Blood Type: O +

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

Race: White Or Caucasian

CMV Status: POS
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Last Medical History Update: 07/28/2020

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

  • Height:
    5'10" (177.8 cm)
    Weight:
    175 lbs (79 kg)
    Eye Color:
    Blue
    Hair Color:
    Brown, Dark
    Hair Texture:
    Thick
    Hair Loss:
    None
    Hair Type:
    Wavy
    Body Build:
    Medium
    Freckles:
    Numerous
    Skin Tone:
    Medium
  • ADVISORY

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

    Below is a list of all conditions for which donor 5499 was tested, including the condition(s) of which he is a carrier. To purchase units from this donor, the intended parent must sign an acknowledgment 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 contact us, and we will provide a copy of the donor's test reports to your physician and/or genetic counselor.

    This donor was tested for 171 conditions.

    Galactosemia, GALT-Related (GALT)
    Carrier of Duarte variant
    Smith-Lemli-Opitz Syndrome (DHCR7)
    Carrier
    Tay-Sachs Disease also known as Hexosaminidase A Deficiency (HEXA)
    Carrier of pseudodeficiency allele
    21-Alpha-Hydroxylase-Deficient Congenital Adrenal Hyperplasia (CYP21A2)
    No disease-causing mutations detected
    3-Hydroxy-3-Methylglutaryl-CoA (HMG-CoA) Lyase Deficiency (HMGCL)
    No disease-causing mutations detected
    3-Methylglutaconic Aciduria Type III also known as Costeff Optic Atrophy (OPA3)
    No disease-causing mutations detected
    6-Pyruvoyl-Tetrahydropterin Synthase Deficiency (PTS)
    No disease-causing mutations detected
    Adenosine Deaminase Deficiency (ADA)
    No disease-causing mutations detected
    Alpha-Mannosidosis (MAN2B1)
    No disease-causing mutations detected
    Alpha-Thalassemia (HBA1/HBA2)
    No disease-causing mutations detected; normal red blood cell indices and hemoglobin analysis
    Alport Syndrome, COL4A3-Related (COL4A3)
    No disease-causing mutations detected
    Alport Syndrome, COL4A4-Related (COL4A4)
    No disease-causing mutations detected
    Alstrom Syndrome (ALMS1)
    No disease-causing mutations detected
    Andermann Syndrome (SLC12A6)
    No disease-causing mutations detected
    Arginase Deficiency also known as Argininemia (ARG1)
    No disease-causing mutations detected
    Argininosuccinic Aciduria (ASL)
    No disease-causing mutations detected
    Aspartylglucosaminuria (AGA)
    No disease-causing mutations detected
    Ataxia With Vitamin E Deficiency (TTPA)
    No disease-causing mutations detected
    Ataxia-Telangiectasia (ATM)
    No disease-causing mutations detected
    Bardet-Biedl Syndrome 13 also known as Meckel Syndrome 1 (MKS1)
    No disease-causing mutations detected
    Bardet-Biedl Syndrome, BBS1-Related (BBS1)
    No disease-causing mutations detected
    Bardet-Biedl Syndrome, BBS10-Related (BBS10)
    No disease-causing mutations detected
    Bardet-Biedl Syndrome, BBS12-Related (BBS12)
    No disease-causing mutations detected
    Bardet-Biedl Syndrome, BBS2-Related (BBS2)
    No disease-causing mutations detected
    Beta-Thalassemia, Sickle Cell Disease, and Beta-Globin Disorders (HBB)
    No disease-causing mutations detected; normal red blood cell indices and hemoglobin analysis
    Biotinidase Deficiency (BTD)
    No disease-causing mutations detected
    Bloom Syndrome (BLM)
    No disease-causing mutations detected
    Canavan Disease (ASPA)
    No disease-causing mutations detected
    Carbamoylphosphate Synthetase I Deficiency (CPS1)
    No disease-causing mutations detected
    Carnitine Palmitoyltransferase IA Deficiency (CPT1A)
    No disease-causing mutations detected
    Carnitine Palmitoyltransferase II Deficiency (CPT2)
    No disease-causing mutations detected
    Cartilage-Hair Hypoplasia (RMRP)
    No disease-causing mutations detected
    Cerebrotendinous Xanthomatosis (CYP27A1)
    No disease-causing mutations detected
    Chromosomal Analysis
    Normal male karyotype
    Citrullinemia Type 1 (ASS1)
    No disease-causing mutations detected
    Cockayne Syndrome Type A (ERCC8)
    No disease-causing mutations detected
    Cockayne Syndrome Type B (ERCC6)
    No disease-causing mutations detected
    Cohen Syndrome (VPS13B)
    No disease-causing mutations detected
    Combined Pituitary Hormone Deficiency 2 (PROP1)
    No disease-causing mutations detected
    Congenital Adrenal Hyperplasia due to 11-Beta-Hydroxylase Deficiency (CYP11B1)
    No disease-causing mutations detected
    Congenital Disorder of Glycosylation Type 1a, PMM2-Related (PMM2)
    No disease-causing mutations detected
    Congenital Disorder of Glycosylation Type 1b (MPI)
    No disease-causing mutations detected
    Congenital Disorder of Glycosylation, Type Ic (ALG6)
    No disease-causing mutations detected
    Cystic Fibrosis and Other CFTR-Related Disorders (CFTR)
    No disease-causing mutations detected
    Cystinosis (CTNS)
    No disease-causing mutations detected
    D-Bifunctional Protein Deficiency (HSD17B4)
    No disease-causing mutations detected
    Delta-Sarcoglycanopathy (SGCD)
    No disease-causing mutations detected
    Dyskeratosis Congenita, RTEL1-Related (RTEL1)
    No disease-causing mutations detected
    Dystrophinopathies, DMD-Related, X-Linked (DMD)
    No disease-causing mutations detected
    Ellis-Van Creveld Syndrome, EVC-Related (EVC)
    No disease-causing mutations detected
    Ellis-Van Creveld Syndrome, EVC2-Related (EVC2)
    No disease-causing mutations detected
    Fabry Disease, X-Linked (GLA)
    No disease-causing mutations detected
    Familial Dysautonomia (IKBKAP)
    No disease-causing mutations detected
    Familial Hyperinsulinism and Other ABCC8-Related Disorders (ABCC8)
    No disease-causing mutations detected
    Familial Hyperinsulinism and Other KCNJ11-Related Disorders (KCNJ11)
    No disease-causing mutations detected
    Familial Mediterranean Fever (MEFV)
    No disease-causing mutations detected
    Fanconi Anemia Type A (FANCA)
    No disease-causing mutations detected
    Fanconi Anemia Type C (FANCC)
    No disease-causing mutations detected
    FKTN-Related Disorders including Walker-Warburg Syndrome (FKTN)
    No disease-causing mutations detected
    Galactokinase Deficiency (GALK1)
    No disease-causing mutations detected
    Gaucher Disease (GBA)
    No disease-causing mutations detected
    GJB2-Related DFNB1 Nonsyndromic Hearing Loss and Deafness (GJB2)
    No disease-causing mutations detected
    Glutaric Acidemia Type 1 (GCDH)
    No disease-causing mutations detected
    Glycine Encephalopathy, AMT-Related (AMT)
    No disease-causing mutations detected
    Glycine Encephalopathy, GLDC-Related (GLDC)
    No disease-causing mutations detected
    Glycogen Storage Disease Type Ia (G6PC)
    No disease-causing mutations detected
    Glycogen Storage Disease Type Ib (SLC37A4)
    No disease-causing mutations detected
    Glycogen Storage Disease Type III (AGL)
    No disease-causing mutations detected
    GRACILE Syndrome (BCS1L)
    No disease-causing mutations detected
    Hereditary Fructose Intolerance (ALDOB)
    No disease-causing mutations detected
    Holocarboxylase Synthetase Deficiency (HLCS)
    No disease-causing mutations detected
    Homocystinuria (CBS)
    No disease-causing mutations detected
    Hydrolethalus Syndrome (HYLS1)
    No disease-causing mutations detected
    Hypophosphatasia, Autosomal Recessive (ALPL)
    No disease-causing mutations detected
    Inclusion Body Myopathy 2 (GNE)
    No disease-causing mutations detected
    Isovaleric Acidemia (IVD)
    No disease-causing mutations detected
    Joubert Syndrome 2 (TMEM216)
    No disease-causing mutations detected
    Junctional Epidermolysis Bullosa (LAMA3)
    No disease-causing mutations detected
    Junctional Epidermolysis Bullosa (LAMB3)
    No disease-causing mutations detected
    Junctional Epidermolysis Bullosa (LAMC2)
    No disease-causing mutations detected
    Krabbe Disease (GALC)
    No disease-causing mutations detected
    Leigh Syndrome, French-Canadian Type (LRPPRC)
    No disease-causing mutations detected
    Limb-Girdle Muscular Dystrophy Type 2A also known as Calpainopathy (CAPN3)
    No disease-causing mutations detected
    Limb-Girdle Muscular Dystrophy Type 2B also known as Dysferlinopathy (DYSF)
    No disease-causing mutations detected
    Limb-Girdle Muscular Dystrophy Type 2C also known as Gamma-Sarcoglycanopathy (SGCG)
    No disease-causing mutations detected
    Limb-Girdle Muscular Dystrophy Type 2D also known as Alpha-Sarcoglycanopathy (SGCA)
    No disease-causing mutations detected
    Limb-Girdle Muscular Dystrophy Type 2E also known as Beta-Sarcoglycanopathy (SGCB)
    No disease-causing mutations detected
    Limb-Girdle Muscular Dystrophy Type 2I (FKRP)
    No disease-causing mutations detected
    Lipoid Adrenal Hyperplasia (STAR)
    No disease-causing mutations detected
    Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (HADHA)
    No disease-causing mutations detected
    Lysosomal Acid Lipase Deficiency including Wolman Disease and Cholesteryl Ester Storage Disease (LIPA)
    No disease-causing mutations detected
    Maple Syrup Urine Disease Type 1A (BCKDHA)
    No disease-causing mutations detected
    Maple Syrup Urine Disease Type 1B (BCKDHB)
    No disease-causing mutations detected
    Maple Syrup Urine Disease Type 2 (DBT)
    No disease-causing mutations detected
    Maple Syrup Urine Disease Type 3 also known as Dihyrolipoamide Dehydrogenase Deficiency (DLD)
    No disease-causing mutations detected
    Medium Chain Acyl-CoA Dehydrogenase Deficiency (ACADM)
    No disease-causing mutations detected
    Megalencephalic Leukoencephalopathy With Subcortical Cysts Type 1 (MLC1)
    No disease-causing mutations detected
    Menkes Disease and Other ATP7A-Related Disorders, X-Linked (ATP7A)
    No disease-causing mutations detected
    Merosin-Deficient Muscular Dystrophy (LAMA2)
    No disease-causing mutations detected
    Metachromatic Leukodystrophy (ARSA)
    No disease-causing mutations detected
    Methylmalonic Acidemia (MMAA)
    No disease-causing mutations detected
    Methylmalonic Acidemia (MMAB)
    No disease-causing mutations detected
    Methylmalonic Acidemia (MUT)
    No disease-causing mutations detected
    Methylmalonic Aciduria and Homocystinuria, Cobalamin C Type (MMACHC)
    No disease-causing mutations detected
    Mucolipidosis II and IIIA (GNPTAB)
    No disease-causing mutations detected
    Mucolipidosis III Gamma (GNPTG)
    No disease-causing mutations detected
    Mucolipidosis Type IV (MCOLN1)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type I also known as Hurler Syndrome (IDUA)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type II also known as Hunter Syndrome, X-Linked (IDS)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type IIIA also known as Sanfilippo A Syndrome (SGSH)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type IIIB also known as Sanfilippo B Syndrome (NAGLU)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type IIIC also known as Sanfilippo C Syndrome (HGSNAT)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type IVb also known as GM1 Gangliosidosis (GLB1)
    No disease-causing mutations detected
    Muscle-Eye-Brain Disease (POMGNT1)
    No disease-causing mutations detected
    Nemaline Myopathy 2 (NEB)
    No disease-causing mutations detected
    Nephrotic Syndrome, NPHS1-Related also known as Congenital Finnish Nephrosis (NPHS1)
    No disease-causing mutations detected
    Nephrotic Syndrome, NPHS2-Related also known as Steroid-Resistant Nephrotic Syndrome (NPHS2)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, CLN3-Related (CLN3)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, CLN5-Related (CLN5)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, CLN6-Related (CLN6)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, CLN8-Related also known as Northern Epilepsy (CLN8)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, PPT1-Related (PPT1)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, TPP1-Related (TPP1)
    No disease-causing mutations detected
    Niemann-Pick Disease Type A/B (SMPD1)
    No disease-causing mutations detected
    Niemann-Pick Disease Type A/B (SMPD1)
    No disease-causing mutations detected
    Niemann-Pick Disease Type C, NPC1-Related (NPC1)
    No disease-causing mutations detected
    Niemann-Pick Disease Type C, NPC2-Related (NPC2)
    No disease-causing mutations detected
    Nijmegen Breakage Syndrome (NBN)
    No disease-causing mutations detected
    Ornithine Transcarbamylase Deficiency, X-Linked (OTC)
    No disease-causing mutations detected
    Osteochondrodysplasias, Sulfate Transporter-Related (SLC26A2)
    No disease-causing mutations detected
    Osteopetrosis Type 1 (TCIRG1)
    No disease-causing mutations detected
    Pendred Syndrome (SLC26A4)
    No disease-causing mutations detected
    Peroxisome Biogenesis Disorder, Type 3 (PEX12)
    No disease-causing mutations detected
    Phenylalanine Hydroxylase Deficiency also known as Phenylketonuria (PAH)
    No disease-causing mutations detected
    Polycystic Kidney Disease, Autosomal Recessive (PKHD1)
    No disease-causing mutations detected
    Polyglandular Autoimmune Syndrome Type 1 (AIRE)
    No disease-causing mutations detected
    Pompe Disease also known as Glycogen Storage Disease Type II (GAA)
    No disease-causing mutations detected
    Primary Carnitine Deficiency (SLC22A5)
    No disease-causing mutations detected
    Primary Hyperoxaluria Type 1 (AGXT)
    No disease-causing mutations detected
    Primary Hyperoxaluria Type 2 (GRHPR)
    No disease-causing mutations detected
    Primary Hyperoxaluria, Type 3 (HOGA1)
    No disease-causing mutations detected
    Propionic Acidemia, PCCA-Related (PCCA)
    No disease-causing mutations detected
    Propionic Acidemia, PCCB-Related (PCCB)
    No disease-causing mutations detected
    Pycnodysostosis (CTSK)
    No disease-causing mutations detected
    Pyruvate Carboxylase Deficiency (PC)
    No disease-causing mutations detected
    Rhizomelic Chondrodysplasia Punctata Type 1 (PEX7)
    No disease-causing mutations detected
    Salla Disease (SLC17A5)
    No disease-causing mutations detected
    Sandhoff Disease (HEXB)
    No disease-causing mutations detected
    Segawa Syndrome (TH)
    No disease-causing mutations detected
    Short Chain Acyl-CoA Dehydrogenase Deficiency (ACADS)
    No disease-causing mutations detected
    Sjogren-Larsson Syndrome (ALDH3A2)
    No disease-causing mutations detected
    Spastic Ataxia of Charlevoix-Saguenay, Autosomal Recessive (SACS)
    No disease-causing mutations detected
    Spastic Paraplegia, Type 15 (ZFYVE26)
    No disease-causing mutations detected
    Spinal Muscular Atrophy (SMN1)
    No disease-causing mutations detected (2 copies detected)
    Spondylothoracic Dysostosis (MESP2)
    No disease-causing mutations detected
    TGM1-Related Autosomal Recessive Congenital Ichthyosis (TGM1)
    No disease-causing mutations detected
    Tyrosinemia Type 1 (FAH)
    No disease-causing mutations detected
    Tyrosinemia, Type II (TAT)
    No disease-causing mutations detected
    Usher Syndrome Type IB (MYO7A)
    No disease-causing mutations detected
    Usher Syndrome Type IC (USH1C)
    No disease-causing mutations detected
    Usher Syndrome Type IF (PCDH15)
    No disease-causing mutations detected
    Usher Syndrome Type IIA (USH2A)
    No disease-causing mutations detected
    Usher Syndrome Type IIIA (CLRN1)
    No disease-causing mutations detected
    Very Long Chain Acyl-CoA Dehydrogenase Deficiency (ACADVL)
    No disease-causing mutations detected
    Wilson Disease (ATP7B)
    No disease-causing mutations detected
    Xeroderma Pigmentosum, Group A (XPA)
    No disease-causing mutations detected
    Xeroderma Pigmentosum, Group C (XPC)
    No disease-causing mutations detected
    Zellweger Spectrum Disorder, PEX1-Related (PEX1)
    No disease-causing mutations detected
    Zellweger Spectrum Disorder, PEX2-Related (PEX2)
    No disease-causing mutations detected
    Zellweger Spectrum Disorder, PEX6-Related (PEX6)
    No disease-causing mutations detected
    Zellweger Syndrome Spectrum, PEX10- Related (PEX10)
    No disease-causing mutations detected
  • Medication Allergy:
    No
    Food Allergy:
    No
    Pet Allergy:
    No
    Hay Fever Allergy:
    No
    Insect Allergy:
    No
    Vaccine Allergy:
    No
    Healthy Teeth:
    Yes
    Braces:
    No
    Back Problems:
    No
    Bronchitis:
    No
    Chicken Pox:
    No
    Chicken Pox Age:
    Vertigo:
    No
    Comments:
    Donor is a Pescatarian.
    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:
    No
    Stomach Ulcers:
    No
  • Skills, Hobbies and Interests:
    Reading, writing, board games, archery, krav maga

  • In School:
    Yes
    Is the donor currently enrolled in or does the donor hold an undergraduate degree?
    Yes
    Degree Earned/Working towards:
    Bachelor of Arts
    Degree Status:
    Graduated
    Major:
    Anthropology
    Minor:
    Environmental Ethics
    Is the donor currently enrolled in or does the donor hold a graduate degree?
    Yes
    Degree Earned/Working towards:
    Master of Arts
    Degree Status:
    Currently enrolled
    Major:
    Anthropology
    Minor:
    Ethnology
    Is the donor currently enrolled in or does the donor hold a post 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
    Sjorgen'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
    VonWillebrand'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 Grandfather X 67
    Cancer (Other) X
    Cancer (Skin) X
    Lymphoma X
    Melanoma 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
    Undescended Testicles X
    Gastro-Intestinal Diseases Yes No Which
    Relative
    Father's
    Side
    Mother's
    Side
    Age of
    Onset
    Gallstones X
    GI (Crohns) X
    GI (Diverticulitis) X
    GI (Other) X
    GI (Pyloric Stenosis) X
    GI (Ulcerative Colitis) X
    GI (Ulcers) X
    Hemochromatosis X
    Hepatitis X
    Kidney Disease 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 of 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
    Acondroplasia (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/ Aspergers 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's) X
    Neurologic (Creutzfeld-Jacob 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 (Neurofibrimatosis) X
    Neurologic (Parkinson's Disease) X
    Neurologic (Subacute Sclerosing Panencephalitis) X
    Nieman-Pick X
    Spongioform 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 (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: Brown, Medium Eyesight:
    Freckles: Few Hair Texture: Fine
    Health Status: Good Skin Tone: Medium Dominant Hand:
    Year of Birth: 1954 Cause of Death: Hair Loss:
    Height: 5'09" (175.26 cm) Age at Death: Body Hair: Straight
    Weight: 170 lbs. (77 kg) Occupation: Carpenter Eye Color: Blue
    Half Siblings: No Education: High School Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision. Enjoys woodworking.
    FAMILY MEMBER: Mother
    Hair Color: Brown, Dark Eyesight:
    Freckles: None Hair Texture: Fine
    Health Status: Good Skin Tone: Medium Dominant Hand:
    Year of Birth: 1954 Cause of Death: Hair Loss:
    Height: 5'05" (165.1 cm) Age at Death: Body Hair: Straight
    Weight: 128 lbs. (58 kg) Occupation: Bookkeeper Eye Color: Hazel/Green
    Half Siblings: No Education: High School Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: She has one dimple on her left cheek. Enjoys sewing, art, and writing.
    FAMILY MEMBER: Brother
    Hair Color: Brown, Medium Eyesight:
    Freckles: Few Hair Texture:
    Health Status: Good Skin Tone: Fair Dominant Hand:
    Year of Birth: 1993 Cause of Death: Hair Loss:
    Height: 5'07" (170.18 cm) Age at Death: Body Hair: Straight
    Weight: 190 lbs. (86 kg) Occupation: Cook Eye Color: Hazel/Green
    Half Siblings: No Education: High School Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has dimples. He’s a very gifted guitar player.
    FAMILY MEMBER: Sister
    Hair Color: Brown, Medium Eyesight:
    Freckles: Few Hair Texture: Fine
    Health Status: Good Skin Tone: Olive Dominant Hand:
    Year of Birth: 1979 Cause of Death: Hair Loss:
    Height: 5'03" (160.02 cm) Age at Death: Body Hair: Straight
    Weight: 115 lbs. (52 kg) Occupation: Cabinet Builder Eye Color: Brown, Light
    Half Siblings: Yes Education: GED Body Build: Small
    Half Siblings Parent: Mother Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision, a Cleft chin, and high cheek bones. She’s a history buff and a collector of fine things.
  • 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: Few Hair Texture: Thick
    Health Status: Good Skin Tone: Medium Dominant Hand:
    Year of Birth: 1937 Cause of Death: Hair Loss:
    Height: 6'" (182.88 cm) Age at Death: Body Hair: Wavy
    Weight: 180 lbs. (81 kg) Occupation: Factory Worker Eye Color: Blue
    Half Siblings: Education: High School Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Enjoys baseball.
    FAMILY MEMBER: Grandmother
    Hair Color: Brown, Dark Eyesight:
    Freckles: Numerous Hair Texture: Thick
    Health Status: Good Skin Tone: Medium Dominant Hand:
    Year of Birth: 1937 Cause of Death: Hair Loss:
    Height: 5'" (152.4 cm) Age at Death: Body Hair: Wavy
    Weight: 95 lbs. (43 kg) Occupation: Homemaker, Retail Sales Eye Color: Brown, Dark
    Half Siblings: Education: High School Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    FAMILY MEMBER: Uncle
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1957 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    FAMILY MEMBER: Uncle
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1960 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    FAMILY MEMBER: Uncle
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1965 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    FAMILY MEMBER: Uncle
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1966 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
  • 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: None Hair Texture:
    Health Status: Skin Tone: Medium Dominant Hand:
    Year of Birth: 1921 Cause of Death: Lung cancer Hair Loss:
    Height: 5'09" (175.26 cm) Age at Death: 67 Body Hair: Straight
    Weight: 180 lbs. (81 kg) Occupation: Military, Small Business Owner Eye Color: Blue
    Half Siblings: Education: College (Some) Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Had corrected vision. He was a master mechanic. Spoke 4 languages. Enjoyed woodworking.
    FAMILY MEMBER: Grandmother
    Hair Color: Brown, Dark Eyesight:
    Freckles: None Hair Texture:
    Health Status: Good Skin Tone: Medium Dominant Hand:
    Year of Birth: 1927 Cause of Death: Hair Loss:
    Height: 5'06" (167.64 cm) Age at Death: Body Hair: Wavy
    Weight: 145 lbs. (65 kg) Occupation: Homemaker Eye Color: Grey
    Half Siblings: Education: High School Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Enjoys needlework/sewing.
    FAMILY MEMBER: Uncle
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Fair Skin Tone: Dominant Hand:
    Year of Birth: 1949 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    FAMILY MEMBER: Uncle
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1951 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    FAMILY MEMBER: Uncle
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1960 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    FAMILY MEMBER: Aunt
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1955 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    FAMILY MEMBER: Aunt
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Fair Skin Tone: Dominant Hand:
    Year of Birth: 1958 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:

Purchase Bundle Options

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Unit Types Available for Donor #5499

All prices shown are in USD.

$1195 per unit Identity Disclosure xyGene Washed

Due to inventory, above prices do not guarantee that listed unit types are currently available. Please contact our team to check availability.

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