Donor Profile : Donor 6767

of Profiles
 in your search results

Donor ID: 6767

Save to Favorites

View Donor Photos

Donor 6767 has more photos.

Click here to view them.

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:
August 2, 2025 5:36 AM EST


Document ID: 8C0795745455DEC15D5AF42D3D9604C197FFB657358C398776F132098AA9ABC5

Sign in or Create an Account to view Enhanced Profile

Donor's "Name": Franklin

Year of Birth: 1994

Marital Status: Single

Number of Children: 0

Occupation:
(last reported)
Bank Teller

Education:

Blood Type: O +

Nationality:
(self reported)
Maternal: Indigenous American
African
Paternal: Irish
African

Race: Black Or African American

CMV Status: NEG
Learn More

Last Medical History Update: 06/07/2018

  • Reported Pregnancy/Birth
  • xyIdentity Disclosure
  • Available Inventory

ADDITIONAL DONOR DETAILS

  • Height:
    6'01" (185.42 cm)
    Weight:
    165 lbs (74 kg)
    Eye Color:
    Brown, Dark
    Hair Color:
    Black
    Hair Texture:
    Thick
    Hair Loss:
    None
    Hair Type:
    Wavy
    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 104 genes.

    21-Alpha-Hydroxylase-Deficient Congenital Adrenal Hyperplasia (CYP21A2)
    No disease-causing variants detected
    3-Methylglutaconic Aciduria Type III also known as Costeff Optic Atrophy (OPA3)
    No disease-causing variants detected
    Achromatopsia (CNGB3)
    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-Thalassemia (HBA1/HBA2)
    No disease-causing mutations detected; normal red blood cell indices and hemoglobin analysis
    Andermann Syndrome (SLC12A6)
    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
    Bardet-Biedl Syndrome, BBS1-Related (BBS1)
    No disease-causing variants detected
    Bardet-Biedl Syndrome, BBS10-Related (BBS10)
    No disease-causing variants 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 variants detected
    Bloom Syndrome (BLM)
    No disease-causing variants detected
    Canavan Disease (ASPA)
    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
    Cartilage-Hair Hypoplasia (RMRP)
    No disease-causing variants detected
    Choroidemia, X-Linked (CHM)
    No disease-causing variants detected
    Chromosome Analysis (Karyotype)
    Normal male karyotype
    Citrullinemia Type 1 (ASS1)
    No disease-causing variants detected
    Cohen Syndrome (VPS13B)
    No disease-causing variants detected
    Combined Pituitary Hormone Deficiency 2 (PROP1)
    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
    Cystic Fibrosis and Other CFTR-Related Disorders (CFTR)
    No disease-causing variants detected
    Cystinosis (CTNS)
    No disease-causing variants detected
    D-Bifunctional Protein Deficiency (HSD17B4)
    No disease-causing variants detected
    Factor XI Deficiency (F11)
    No disease-causing variants detected
    Familial Dysautonomia (IKBKAP)
    No disease-causing variants detected
    Familial Hyperinsulinism and Other ABCC8-Related Disorders (ABCC8)
    No disease-causing variants detected
    Familial Mediterranean Fever (MEFV)
    No disease-causing variants detected
    Fanconi Anemia Type C (FANCC)
    No disease-causing variants detected
    Galactosemia, GALT-Related (GALT)
    No disease-causing variants detected
    Gaucher Disease (GBA)
    No disease-causing variants detected
    GJB2-Related DFNB1 Nonsyndromic Hearing Loss and Deafness (GJB2)
    No disease-causing variants detected
    Glutaric Acidemia Type 1 (GCDH)
    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 V (PYGM)
    No disease-causing variants detected
    GRACILE Syndrome (BCS1L)
    No disease-causing variants detected
    Hereditary Fructose Intolerance (ALDOB)
    No disease-causing variants detected
    Hereditary Thymine-Uraciluria also known as Dihydropyrimidine Dehydrogenase Deficiency (DPYD)
    No disease-causing variants detected
    Homocystinuria (CBS)
    No disease-causing variants detected
    Hypophosphatasia, Autosomal Recessive (ALPL)
    No disease-causing variants detected
    Inclusion Body Myopathy 2 (GNE)
    No disease-causing variants detected
    Isovaleric Acidemia (IVD)
    No disease-causing variants detected
    Joubert Syndrome 2 (TMEM216)
    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
    Juvenile Retinoschisis, X-Linked (RS1)
    No disease-causing variants detected
    Krabbe Disease (GALC)
    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
    Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (HADHA)
    No disease-causing variants detected
    Maple Syrup Urine Disease Type 1B (BCKDHB)
    No disease-causing variants detected
    Maple Syrup Urine Disease Type 3 also known as Dihyrolipoamide Dehydrogenase Deficiency (DLD)
    No disease-causing variants detected
    Medium Chain Acyl-CoA Dehydrogenase Deficiency (ACADM)
    No disease-causing variants detected
    Megalencephalic Leukoencephalopathy With Subcortical Cysts Type 1 (MLC1)
    No disease-causing variants detected
    Metachromatic Leukodystrophy (ARSA)
    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
    Muscle-Eye-Brain Disease (POMGNT1)
    No disease-causing variants detected
    Nemaline Myopathy 2 (NEB)
    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, CLN3-Related (CLN3)
    No disease-causing variants detected
    Neuronal Ceroid-Lipofuscinosis, CLN5-Related (CLN5)
    No disease-causing variants detected
    Neuronal Ceroid-Lipofuscinosis, CLN8-Related also known as Northern Epilepsy (CLN8)
    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 A/B (SMPD1)
    No disease-causing variants detected
    Niemann-Pick Disease Type C, NPC1-Related (NPC1)
    No disease-causing variants detected
    Nijmegen Breakage Syndrome (NBN)
    No disease-causing variants detected
    Osteochondrodysplasias, Sulfate Transporter-Related (SLC26A2)
    No disease-causing variants detected
    Pendred Syndrome (SLC26A4)
    No disease-causing variants detected
    Phenylalanine Hydroxylase Deficiency also known as Phenylketonuria (PAH)
    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
    Pompe Disease also known as Glycogen Storage Disease Type II (GAA)
    No disease-causing variants detected
    Primary Carnitine Deficiency (SLC22A5)
    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
    Pseudocholinesterase Deficiency (BCHE)
    No disease-causing variants detected
    Pycnodysostosis (CTSK)
    No disease-causing variants detected
    Rhizomelic Chondrodysplasia Punctata Type 1 (PEX7)
    No disease-causing variants detected
    Salla Disease (SLC17A5)
    No disease-causing variants detected
    Segawa Syndrome (TH)
    No disease-causing variants detected
    Short Chain Acyl-CoA Dehydrogenase Deficiency (ACADS)
    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
    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 variants detected
    Tyrosinemia Type 1 (FAH)
    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
    Very Long Chain Acyl-CoA Dehydrogenase Deficiency (ACADVL)
    No disease-causing variants detected
    Wilson Disease (ATP7B)
    No disease-causing variants detected
    Zellweger Spectrum Disorder, PEX1-Related (PEX1)
    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:
    No
    Back Problems:
    No
    Bronchitis:
    No
    Chicken Pox:
    Yes
    Chicken Pox Age:
    2
    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:
    Basketball, Business, Cooking, Exercising, Football, Mathematics, Philosophy, Public Speaking, Reading, Sales, Traveling

  • In School:
    Yes
    In School Major:
    Business Accounting
    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 Grandmother X 34
    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 Grandfather X 55
    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 (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
    Fragile X X
    Klinefelter X
    Noonan or Turner Syndrome X
    Other - Early Death X Grandmother X 34
    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, Medium Dominant Hand:
    Year of Birth: 1989 Cause of Death: Hair Loss:
    Height: 5'04" (162.56 cm) Age at Death: Body Hair: Wavy
    Weight: 138 lbs. (62 kg) Occupation: Insurance Customer Service Eye Color: Brown, Dark
    Half Siblings: No Education: College Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision. Enjoys music and sports.
    FAMILY MEMBER: Brother
    Hair Color: Black Eyesight:
    Freckles: None Hair Texture:
    Health Status: Good Skin Tone: Brown, Medium Dominant Hand: Left
    Year of Birth: 1987 Cause of Death: Hair Loss:
    Height: 5'08" (172.72 cm) Age at Death: Body Hair: Wavy
    Weight: 180 lbs. (81 kg) Occupation: Contractor Tech for Comcast Eye Color: Brown, Dark
    Half Siblings: No Education: College Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: He’s left-handed. Enjoys basketball, football, reading, film, music, golf, and boarding.
    FAMILY MEMBER: Father
    Hair Color: Black Eyesight:
    Freckles: None Hair Texture:
    Health Status: Good Skin Tone: Black Dominant Hand:
    Year of Birth: 1967 Cause of Death: Hair Loss:
    Height: 5'09" (175.26 cm) Age at Death: Body Hair: Straight
    Weight: 185 lbs. (83 kg) Occupation: Engineer for Oil Company Eye Color: Brown, Dark
    Half Siblings: No Education: College Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Enjoys traveling, reading, watching movies, writing, and cars.
    FAMILY MEMBER: Mother
    Hair Color: Black Eyesight:
    Freckles: None Hair Texture:
    Health Status: Good Skin Tone: Brown, Light Dominant Hand: Left
    Year of Birth: 1967 Cause of Death: Hair Loss:
    Height: 5'06" (167.64 cm) Age at Death: Body Hair: Curly
    Weight: 105 lbs. (47 kg) Occupation: Analyst for CDC Eye Color: Brown, Light
    Half Siblings: No Education: College Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision and is left-handed. She’s very generous. Enjoys traveling, dancing old school slides, singing, cooking, and financial advising.
  • 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: Deceased Skin Tone: Brown, Dark Dominant Hand:
    Year of Birth: 1930 Cause of Death: Old Age Hair Loss:
    Height: 5'11" (180.34 cm) Age at Death: 65 Body Hair: Straight
    Weight: 180 lbs. (81 kg) Occupation: Former Custodian, Painter, Cook Eye Color: Black
    Half Siblings: Education: College (Some) Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Enjoyed cooking, and working with others. He cooked for the Tuskegee Airmen at an airfield.
    FAMILY MEMBER: Grandmother
    Hair Color: Black Eyesight:
    Freckles: None Hair Texture:
    Health Status: Good Skin Tone: Black Dominant Hand:
    Year of Birth: 1947 Cause of Death: Hair Loss:
    Height: 5'07" (170.18 cm) Age at Death: Body Hair: Straight
    Weight: 200 lbs. (90 kg) Occupation: Retired Teacher Eye Color: Brown, Dark
    Half Siblings: Education: College Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Enjoys reading, writing, and walking.
  • 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: Good Skin Tone: Brown, Dark Dominant Hand:
    Year of Birth: 1937 Cause of Death: Hair Loss:
    Height: 5'11" (180.34 cm) Age at Death: Body Hair: Wavy
    Weight: 207 lbs. (93 kg) Occupation: Food Industry, Shoemaker Eye Color: Brown, Dark
    Half Siblings: Education: High School Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Enjoys basketball, football, and music.
    Health Condition: High Blood Pressure at age 55
    FAMILY MEMBER: Grandmother
    Hair Color: Black Eyesight:
    Freckles: None Hair Texture:
    Health Status: Deceased Skin Tone: Brown, Light Dominant Hand:
    Year of Birth: 1939 Cause of Death: Breast Cancer Hair Loss:
    Height: 5'06" (167.64 cm) Age at Death: 34 Body Hair: Curly
    Weight: 132 lbs. (59 kg) Occupation: Homemaker Eye Color: Brown, Light
    Half Siblings: Education: High School Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Health Condition: Cancer (Breast) at age 34
    Health Condition: Other - Early Death at age 34
    Breast Cancer
    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: 1962 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: 1964 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

Purchase Bundle Options

No vials are available for this donor at this time. If you would like more info about this donor, please contact us.