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Donor Profile : Donor 3122

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Retired Donor

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Donor ID: 3122

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Meet The Donor

Extremely athletic, his list of sports is extensive. He doesn't just dabble, either. He's all in, whether it's mountain bike racing, soccer, basketball, ultimate frisbee, skateboarding, or baseball, Donor 3122 loves staying fit. He's a history buff, too, having studied sports history, Aboriginal History, and garden history and mythology. Speaking of, he comes from a long line of gardeners, and is a Certified Nursery Professional who enjoys growing his own food.

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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:
June 3, 2023 8:22 PM EST


Document ID: DB85EE7E33CA6868B775FEF9EF510C747E97C8FACBEAE4625C802649A777F62E

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Donor's "Name": Cedric

Year of Birth: 1982

Marital Status: Married

Number of Children: 0

Occupation:
(last reported) College Graduate

Education: Bachelor of Science in Agriculture, Horticulture, Bachelor of Business Administration, Management

Blood Type: O +

Nationality:
(self reported) Maternal: Irish
Scottish
Paternal: Irish
Scottish

Race: White Or Caucasian

CMV Status: NEG
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Last Medical History Update: 06/28/2019

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

  • Height:
    6'2" (187.96 cm)
    Weight:
    237 lbs (107 kg)
    Eye Color:
    Brown
    Hair Color:
    Brown
    Hair Texture:
    Fine
    Hair Loss:
    None
    Hair Type:
    Straight
    Body Build:
    Large
    Freckles:
    Few
    Skin Tone:
    Fair

  • 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 43 conditions.

    3-Phosphoglycerate Dehydrogenase Deficiency, PHGDH-Related (PHGDH)
    No disease-causing mutations detected
    Abetalipoproteinemia (MTTP)
    No disease-causing mutations detected
    Alpha-Thalassemia
    Normal complete blood count and hemoglobin analysis; does not exclude silent carrier status or alpha thalassemia minor
    Alport Syndrome, COL4A3-Related (COL4A3)
    No disease-causing mutations detected
    Arthrogryposis, Mental Retardation, and Seizures (AMRS)
    No disease-causing mutations detected
    Bardet-Biedl Syndrome, BBS2-Related (BBS2)
    No disease-causing mutations detected
    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
    Carnitine Palmitoyltransferase II Deficiency (CPT2)
    No disease-causing mutations detected
    Chromosome Analysis (Karyotype)
    Normal male karyotype
    Congenital Amegakaryocytic Thrombocytopenia (MPL)
    No disease-causing mutations detected
    Congenital Disorder of Glycosylation Type 1a, PMM2-Related (PMM2)
    No disease-causing mutations detected
    Cystic Fibrosis and Other CFTR-Related Disorders (CFTR)
    No disease-causing mutations detected
    Dyskeratosis Congenita, RTEL1-Related (RTEL1)
    No disease-causing mutations detected
    Ehlers-Danlos Syndrome, Type VIIC (ADAMTS2)
    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
    Galactosemia, GALT-Related (GALT)
    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
    Multiple Sulphatase Deficiency (SUMF1)
    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
    Polycystic Kidney Disease, Autosomal Recessive (PKHD1)
    No disease-causing mutations detected
    Retinitis Pigmentosa 59 (DHDDS)
    No disease-causing mutations detected
    Sickle Cell Disease
    Normal complete blood count and hemoglobin analysis
    Smith-Lemli-Opitz Syndrome (DHCR7)
    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
    Tyrosinemia Type 1 (FAH)
    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
    Wilson Disease (ATP7B)
    No disease-causing mutations detected
    Zellweger Spectrum Disorder, PEX2-Related (PEX2)
    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:
    Yes
    Back Problems:
    No
    Bronchitis:
    No
    Chicken Pox:
    Yes
    Chicken Pox Age:
    7
    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:
    Photography, Gardening, Basketball, Weightlifting

  • 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 in Agriculture
    Degree Status:
    Graduated
    Major:
    Horticulture
    Minor:
    N/A
    Degree Earned/Working towards:
    Bachelor of Business Administration
    Degree Status:
    Graduated
    Major:
    Management
    Minor:
    N/A
    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 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.)?
    Yes
    Type Of Training:
    Master Gardener
    Training Body:
    Certificate(s) 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 (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 Grandfather,Grandmother X 92,93
    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 (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 or urinary tract disorder X Grandmother X 90
    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 Grandfather X 87
    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
    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 Donor Conceived Child* N/A
    Eczema X
    Pigmentation disorders (including Vitiligo) X
    Psoriasis X
    Skin Disease X
    *Donor-Conceived Child refers to a child conceived with the donor’s sperm by a Xytex client, not a child of the donor and his reproductive partner.
    Comments:
    The donor has not been tested to confirm that he is a carrier of oculocutaneous albinism.

  • 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, Dark Eyesight:
    Freckles: Few Hair Texture:
    Health Status: Good Skin Tone: Fair Dominant Hand:
    Year of Birth: 1951 Cause of Death: Hair Loss:
    Height: 6'04" (193.04 cm) Age at Death: Body Hair: Straight
    Weight: 190 lbs. (86 kg) Occupation: Real Estate Lawyer Eye Color: Brown, Dark
    Half Siblings: No Education: College Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: He plays cello weekly at assisted living facilities for senior citizens. Also plays piano, racquetball, tennis, and basketball.
    FAMILY MEMBER: Mother
    Hair Color: Brown, Dark Eyesight:
    Freckles: Few Hair Texture:
    Health Status: Good Skin Tone: Fair Dominant Hand:
    Year of Birth: 1953 Cause of Death: Hair Loss:
    Height: 5'08" (172.72 cm) Age at Death: Body Hair: Straight
    Weight: 140 lbs. (63 kg) Occupation: Retired Nurse, Homemaker Eye Color: Brown, Dark
    Half Siblings: No Education: College Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: She is part of the choir at church and an avid singer. Loves to cook, play piano, garden, and donate time to charity.
    FAMILY MEMBER: Brother
    Hair Color: Red, Dark Eyesight:
    Freckles: Few Hair Texture:
    Health Status: Good Skin Tone: Fair Dominant Hand:
    Year of Birth: 1985 Cause of Death: Hair Loss:
    Height: 6'03" (190.5 cm) Age at Death: Body Hair: Straight
    Weight: 150 lbs. (68 kg) Occupation: Website Manager/ Content Developer Eye Color: Brown, Dark
    Half Siblings: No Education: Masters Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: He loves to live a frugal lifestyle and learn how to make things from scratch. Enjoys computer programming, yoga, and hiking.

  • 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: Few Hair Texture:
    Health Status: Skin Tone: Fair Dominant Hand:
    Year of Birth: 1920 Cause of Death: Dementia Hair Loss: Receding
    Height: 6'02" (187.96 cm) Age at Death: 88 Body Hair:
    Weight: 200 lbs. (90 kg) Occupation: College Educator Eye Color: Brown, Dark
    Half Siblings: Education: Ph.D. Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: He was constantly trying to improve the education of others in locations he traveled to around the world (process development). Enjoyed sailing and traveling the world.
    FAMILY MEMBER: Grandmother
    Hair Color: Brown, Medium Eyesight:
    Freckles: Few Hair Texture:
    Health Status: Skin Tone: Fair Dominant Hand:
    Year of Birth: 1924 Cause of Death: Kidney failure Hair Loss:
    Height: 5'06" (167.64 cm) Age at Death: 90 Body Hair: Straight
    Weight: 130 lbs. (59 kg) Occupation: Homemaker Eye Color: Brown, Dark
    Half Siblings: Education: College Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: She collected roses and had over 50 varieties in her garden. Enjoyed cooking, gardening, knitting, and crocheting.

  • 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: Few Hair Texture:
    Health Status: Skin Tone: Fair Dominant Hand:
    Year of Birth: 1920 Cause of Death: Heart attack Hair Loss: Receding
    Height: 6'01" (185.42 cm) Age at Death: 92 Body Hair: Straight
    Weight: 170 lbs. (77 kg) Occupation: Accountant Eye Color: Brown, Light
    Half Siblings: Education: Masters Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: He built cabinets and dressers in his wood shop for my parents and other relatives. Enjoyed flying planes, sailing, and hunting.
    FAMILY MEMBER: Grandmother
    Hair Color: Brown, Light Eyesight:
    Freckles: Few Hair Texture:
    Health Status: Skin Tone: Fair Dominant Hand:
    Year of Birth: 1922 Cause of Death: Heart attack Hair Loss:
    Height: 5'04" (162.56 cm) Age at Death: 93 Body Hair: Straight
    Weight: 120 lbs. (54 kg) Occupation: Homemaker Eye Color: Brown, Light
    Half Siblings: Education: College Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: She knitted blankets that I used as a kid. Enjoyed gardening and cooking.

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Vial Types Available for Donor #3122

All prices shown are in USD.

$1125 per vial xyIdentity Disclosure Washed

$1125 per vial xyIdentity Disclosure Unwashed

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

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