Donor Profile : Donor 5371

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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This donor is no longer active in the program.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: 5371

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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 24, 2024 10:32 PM EST


Document ID: C2495B76E081B8311F6A0660C29FF9B27B7EB1795CE0DDA3B006DF3FEBF91AF6

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Donor's "Name": Amari

Year of Birth: 1995

Marital Status: Single

Number of Children: 0

Occupation:
(last reported)
Student

Education:

Blood Type: A +

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

Race: Asian

CMV Status: POS
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Last Medical History Update: 09/12/2017

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

ADDITIONAL DONOR DETAILS

  • Height:
    6'02" (187.96 cm)
    Weight:
    171 lbs (77 kg)
    Eye Color:
    Black
    Hair Color:
    Black
    Hair Texture:
    Thick
    Hair Loss:
    None
    Hair Type:
    Average
    Body Build:
    Medium
    Freckles:
    None
    Skin Tone:
    Brown, 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 24 genes.

    Alpha-Thalassemia
    Normal complete blood count and hemoglobin analysis; does not exclude silent carrier status or alpha thalassemia minor
    Beta-Thalassemia
    Normal complete blood count and hemoglobin analysis
    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
    FKTN-Related Disorders including Walker-Warburg Syndrome (FKTN)
    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 1A (BCKDHA)
    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
    Sickle Cell Disease
    Normal complete blood count and hemoglobin analysis
    Spinal Muscular Atrophy (SMN1)
    No disease-causing mutations detected (3 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 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:
    Golf, Guitar

  • In School:
    Yes
    In School Major:
    Supply Chain Engineering
    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 Grandfather X 45
    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
    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: Black Eyesight:
    Freckles: None Hair Texture:
    Health Status: Good Skin Tone: Brown, Light Dominant Hand:
    Year of Birth: 1999 Cause of Death: Hair Loss:
    Height: 5'02" (157.48 cm) Age at Death: Body Hair: Straight
    Weight: 110 lbs. (49 kg) Occupation: Student Eye Color: Black
    Half Siblings: No Education: High School Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: He has a Widow’s Peak. Enjoys video games, basketball, and soccer.
    FAMILY MEMBER: Father
    Hair Color: Black Eyesight:
    Freckles: None Hair Texture:
    Health Status: Good Skin Tone: Brown, Medium Dominant Hand:
    Year of Birth: 1963 Cause of Death: Hair Loss:
    Height: 5'10" (177.8 cm) Age at Death: Body Hair: Straight
    Weight: 220 lbs. (99 kg) Occupation: Statistics Professor Eye Color: Black
    Half Siblings: No Education: Ph.D. Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: He has large ears. Enjoys poker.
    FAMILY MEMBER: Mother
    Hair Color: Black Eyesight:
    Freckles: None Hair Texture:
    Health Status: Good Skin Tone: Brown, Dark Dominant Hand:
    Year of Birth: 1965 Cause of Death: Hair Loss:
    Height: 5'01" (154.94 cm) Age at Death: Body Hair: Straight
    Weight: 150 lbs. (68 kg) Occupation: Accountant Eye Color: Black
    Half Siblings: No Education: College Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: She has a Roman nose. Enjoys reading.
  • 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:
    Freckles: None Hair Texture:
    Health Status: Fair Skin Tone: Brown, Light Dominant Hand:
    Year of Birth: 1940 Cause of Death: Hair Loss:
    Height: 5'08" (172.72 cm) Age at Death: Body Hair: Straight
    Weight: 190 lbs. (86 kg) Occupation: Accountant Eye Color: Black
    Half Siblings: Education: College Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Health Condition: Diabetes (Insulin Dependent) at age 45
    FAMILY MEMBER: Grandmother
    Hair Color: Black Eyesight:
    Freckles: None Hair Texture:
    Health Status: Good Skin Tone: Brown, Medium Dominant Hand:
    Year of Birth: 1943 Cause of Death: Hair Loss: Thinning
    Height: 5'02" (157.48 cm) Age at Death: Body Hair:
    Weight: 160 lbs. (72 kg) Occupation: Homemaker Eye Color: Black
    Half Siblings: Education: High School Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: She enjoys knitting.
  • 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:
    Freckles: None Hair Texture:
    Health Status: Fair Skin Tone: Brown, Dark Dominant Hand:
    Year of Birth: 1937 Cause of Death: Hair Loss:
    Height: 5'08" (172.72 cm) Age at Death: Body Hair: Straight
    Weight: 170 lbs. (77 kg) Occupation: Entrepreneur Eye Color: Black
    Half Siblings: Education: College Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: He has dimples.
    FAMILY MEMBER: Grandmother
    Hair Color: Black Eyesight:
    Freckles: None Hair Texture:
    Health Status: Fair Skin Tone: Fair Dominant Hand:
    Year of Birth: 1939 Cause of Death: Hair Loss:
    Height: 5'00" (152.4 cm) Age at Death: Body Hair: Wavy
    Weight: 120 lbs. (54 kg) Occupation: Homemaker Eye Color: Brown, Dark
    Half Siblings: Education: College (Some) Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: She has dimples and a Widow’s Peak.

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