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Donor Profile : Donor 5506

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Donor ID: 5506

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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 26, 2024 11:13 PM EST


Document ID: A4CE428D4216995BD83049C518112F01CF34BBBB72DC5ADDB1F7EBDAF1E90F05

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Donor's "Name": Dean

Year of Birth: 1992

Marital Status: Single

Number of Children: 0

Occupation:
(last reported) Emergency Care Tech

Education: Advanced EMT, AEMT, Nursing, Nursing

Blood Type: O -

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

Race: White Or Caucasian

CMV Status: POS
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Last Medical History Update: 06/10/2020

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

  • Height:
    5'11" (180.34 cm)
    Weight:
    205 lbs (93 kg)
    Eye Color:
    Brown
    Hair Color:
    Brown
    Hair Texture:
    Thick
    Hair Loss:
    None
    Hair Type:
    Wavy
    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 42 genes.

    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:
    4
    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:
    Anything outdoors and spending time with family and friends

  • In School:
    Yes
    Is the donor currently enrolled in or does the donor hold an undergraduate degree?
    Yes
    Degree Earned/Working towards:
    Advanced EMT
    Degree Status:
    Graduated
    Major:
    AEMT
    Minor:
    AEMT
    Is the donor currently enrolled in or does the donor hold a graduate degree?
    Yes
    Degree Earned/Working towards:
    Nursing
    Degree Status:
    Currently enrolled
    Major:
    Nursing
    Minor:
    Nursing
    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:
    AEMT
    Training Body:
    Technical College
    Certificate(s) Earned:
    AEMT

  • 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 Grandmother X 81
    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
    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
    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
    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 (Red-Green 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: Black Eyesight:
    Freckles: None Hair Texture:
    Health Status: Good Skin Tone: Medium Dominant Hand:
    Year of Birth: 1961 Cause of Death: Hair Loss:
    Height: 6'05" (195.58 cm) Age at Death: Body Hair: Wavy
    Weight: 235 lbs. (106 kg) Occupation: Program Manager Eye Color: Brown, Dark
    Half Siblings: No Education: College Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision. Great with computers and loves to sing.
    FAMILY MEMBER: Mother
    Hair Color: Blonde, Light Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Medium Dominant Hand:
    Year of Birth: 1960 Cause of Death: Hair Loss:
    Height: 5'03" (160.02 cm) Age at Death: Body Hair: Curly
    Weight: 145 lbs. (65 kg) Occupation: Recruiting Firm Owner Eye Color: Hazel/Green
    Half Siblings: No Education: College (Some) Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Enjoys tennis, billiards, rollerblading, and hiking.
    FAMILY MEMBER: Sister
    Hair Color: Blonde, Medium Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Medium Dominant Hand:
    Year of Birth: 1989 Cause of Death: Hair Loss:
    Height: 5'08" (172.72 cm) Age at Death: Body Hair: Curly
    Weight: 130 lbs. (59 kg) Occupation: Recruiter and Yoga/Pilates Instructor Eye Color: Brown, Dark
    Half Siblings: No Education: College Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: She’s very interested in organic food and being healthy. Enjoys yoga, hiking, and Pilates.

  • 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: Medium Dominant Hand:
    Year of Birth: 1940 Cause of Death: Hair Loss:
    Height: 5'10" (177.8 cm) Age at Death: Body Hair: Wavy
    Weight: 220 lbs. (99 kg) Occupation: Farmer Eye Color: Hazel/Green
    Half Siblings: Education: High School Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: He’s very strong mentally and physically.
    FAMILY MEMBER: Grandmother
    Hair Color: Black Eyesight:
    Freckles: None Hair Texture:
    Health Status: Good Skin Tone: Medium Dominant Hand:
    Year of Birth: 1941 Cause of Death: Hair Loss:
    Height: 5'08" (172.72 cm) Age at Death: Body Hair: Wavy
    Weight: 160 lbs. (72 kg) Occupation: Farmer Eye Color: Brown, Dark
    Half Siblings: Education: High School Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision. She’s a great cook.

  • 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, Light Eyesight:
    Freckles: Hair Texture:
    Health Status: Skin Tone: Medium Dominant Hand:
    Year of Birth: 1935 Cause of Death: Old age Hair Loss:
    Height: 5'08" (172.72 cm) Age at Death: 82 Body Hair: Wavy
    Weight: 180 lbs. (81 kg) Occupation: Mechanical Engineer Eye Color: Blue
    Half Siblings: Education: College (Some) Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Enjoyed golf and billiards.
    FAMILY MEMBER: Grandmother
    Hair Color: Brown, Dark Eyesight:
    Freckles: Hair Texture:
    Health Status: Skin Tone: Medium Dominant Hand:
    Year of Birth: 1935 Cause of Death: Cancer Hair Loss:
    Height: 5'01" (154.94 cm) Age at Death: 81 Body Hair: Wavy
    Weight: 150 lbs. (68 kg) Occupation: Textile Worker Eye Color: Brown, Dark
    Half Siblings: Education: High School Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Enjoyed knitting.

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$1195 per vial xyIdentity Disclosure Washed

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