Donor Profile : Donor 4927

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This is an xyLimited Donor.

xyLimited Donors are restricted to 15 worldwide family units. Clients must purchase at least 3 vials.

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*Family units are determined by the number of births reported by clients, the geographical location of reported births, and the amount of time a donor is participating in the program.

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This donor is no longer active in the program.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: 4927

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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:
April 19, 2024 5:23 AM EST


Document ID: D3C85D149D52510D2E2DA1FB0510D4CC03F2421CCE4A9BE180624E632BA18526

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Donor's "Name": Byron

Year of Birth: 1989

Marital Status: Single

Number of Children: 0

Occupation:
(last reported)
Student

Education:

Blood Type: O +

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

Race: Hispanic Or Latino

CMV Status: POS
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Last Medical History Update: 12/30/2015

  • Reported Pregnancy/Birth
  • xyIdentity Disclosure
  • Available Inventory
  • Retired

ADDITIONAL DONOR DETAILS

  • Height:
    5'08" (172.72 cm)
    Weight:
    148 lbs (67 kg)
    Eye Color:
    Brown, Dark
    Hair Color:
    Brown, Dark
    Hair Texture:
    Average
    Hair Loss:
    None
    Hair Type:
    Straight
    Body Build:
    Medium
    Freckles:
    None
    Skin Tone:
    Medium
  • 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 21 genes.

    Beta-Thalassemia, Sickle Cell Disease, and Beta-Globin Disorders (HBB)
    No disease-causing mutations detected; normal complete blood count
    Bloom Syndrome (BLM)
    No disease-causing mutations detected
    Canavan Disease (ASPA)
    No disease-causing mutations detected
    Chromosome Analysis (Karyotype)
    Normal male karyotype
    Cystic Fibrosis and Other CFTR-Related Disorders (CFTR)
    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
    Fanconi Anemia Type C (FANCC)
    No disease-causing mutations detected
    Gaucher Disease (GBA)
    No disease-causing mutations detected
    Glycogen Storage Disease Type Ia (G6PC)
    No disease-causing mutations detected
    Joubert Syndrome 2 (TMEM216)
    No disease-causing mutations detected
    Maple Syrup Urine Disease Type 1B (BCKDHB)
    No disease-causing mutations detected
    Maple Syrup Urine Disease Type 3 also known as Dihyrolipoamide Dehydrogenase Deficiency (DLD)
    No disease-causing mutations detected
    Mucolipidosis Type IV (MCOLN1)
    No disease-causing mutations detected
    Nemaline Myopathy 2 (NEB)
    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
    Spinal Muscular Atrophy (SMN1)
    No disease-causing mutations detected (2 copies detected)
    Tay-Sachs Disease also known as Hexosaminidase A Deficiency (HEXA)
    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
  • 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
    Eyesight Correction:
    No
    Near or Far Sighted:
    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:
    Cooking, Hiking, Reading

  • In School:
    Yes
    In School Major:
    Business
    Post Graduate:
    No
    Training Type:
    Degrees Earned:
  • 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 (Lung) X
    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
    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 (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 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
    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
    ADD or ADHD X
    Autism/ Asperger X
    Canavan's disease X
    Cerebral Palsy 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 (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 (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
    Fragile X X
    Klinefelter X
    Noonan or Turner Syndrome X
    Other - Early Death X Grandfather X 23
    Other - Early Death X Grandmother X 44
    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 (Glaucoma) X
    Eyesight (Other) X
    Eyesight (Red-Green Color Blindness) 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: Brother
    Hair Color: Brown, Medium Eyesight: Good
    Freckles: None Hair Texture: Average
    Health Status: Good Skin Tone: Fair Dominant Hand: Right
    Year of Birth: 1987 Cause of Death: Hair Loss: None
    Height: 5'10" (177.8 cm) Age at Death: Body Hair: Straight
    Weight: 175 lbs. (79 kg) Occupation: Lab Technician Eye Color: Brown, Dark
    Half Siblings: No Education: College Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    FAMILY MEMBER: Father
    Hair Color: Black Eyesight: Good
    Freckles: None Hair Texture: Average
    Health Status: Good Skin Tone: Medium Dominant Hand: Right
    Year of Birth: 1952 Cause of Death: Hair Loss: None
    Height: 5'10" (177.8 cm) Age at Death: Body Hair: Straight
    Weight: 185 lbs. (83 kg) Occupation: Chef Eye Color: Brown, Dark
    Half Siblings: No Education: College (Some) Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    FAMILY MEMBER: Mother
    Hair Color: Brown, Medium Eyesight: Excellent
    Freckles: None Hair Texture: Fine
    Health Status: Good Skin Tone: Medium Dominant Hand: Right
    Year of Birth: 1966 Cause of Death: Hair Loss: None
    Height: 5'05" (165.1 cm) Age at Death: Body Hair: Straight
    Weight: 125 lbs. (56 kg) Occupation: Homemaker Eye Color: Black
    Half Siblings: No Education: High School Body Build: Medium
    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: Good
    Freckles: None Hair Texture: Average
    Health Status: Deceased Skin Tone: Medium Dominant Hand: Right
    Year of Birth: 1921 Cause of Death: Natural Causes Hair Loss: None
    Height: 5'11" (180.34 cm) Age at Death: 83 Body Hair: Straight
    Weight: 190 lbs. (86 kg) Occupation: Telegrapher Eye Color: Black
    Half Siblings: Education: High School Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    FAMILY MEMBER: Grandmother
    Hair Color: Black Eyesight: Good
    Freckles: Hair Texture: Fine
    Health Status: Deceased Skin Tone: Fair Dominant Hand: Right
    Year of Birth: 1930 Cause of Death: Natural Causes Hair Loss: None
    Height: 5'05" (165.1 cm) Age at Death: 79 Body Hair: Wavy
    Weight: 140 lbs. (63 kg) Occupation: Homemaker Eye Color: Hazel/Green
    Half Siblings: Education: High School Body Build: Small
    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: Black Eyesight: Good
    Freckles: None Hair Texture:
    Health Status: Deceased Skin Tone: Brown, Light Dominant Hand: Right
    Year of Birth: 1943 Cause of Death: Work Accident Hair Loss: None
    Height: 5'10" (177.8 cm) Age at Death: 23 Body Hair: Straight
    Weight: 130 lbs. (59 kg) Occupation: Construction Worker Eye Color: Black
    Half Siblings: Education: High School Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Health Condition: Other - Early Death at age 23
    Work Accident
    FAMILY MEMBER: Grandmother
    Hair Color: Brown, Dark Eyesight: Good
    Freckles: Hair Texture:
    Health Status: Deceased Skin Tone: Fair Dominant Hand: Right
    Year of Birth: 1944 Cause of Death: Motor Vehicle Accident Hair Loss: None
    Height: 5'06" (167.64 cm) Age at Death: 44 Body Hair: Straight
    Weight: 140 lbs. (63 kg) Occupation: Homemaker Eye Color: Brown, Dark
    Half Siblings: Education: High School Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Health Condition: Other - Early Death at age 44
    Motor Vehicle Accident

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Vial Types Available for Donor #4927

All prices shown are in USD.

$1650 per vial Identity Disclosure xyLimited Washed

$1650 per vial Identity Disclosure xyLimited Unwashed

$1050 per vial Identity Disclosure xyLimited ART

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