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Donor Profile : Donor 92107

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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This donor is no longer active in the program.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: 92107

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Meet The Donor

Donor 92107 is very close to his family, thanks to a series of moves during his childhood. So much so, his sister is his hero. In his spare time, he plays tennis and tries not to watch too much YouTube.

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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:
November 22, 2024 2:56 AM EST


Document ID: 1CAC047A84FC2C152C88FAEDD77EC0085E4841F4E89F457A41A2BDB26E2F8A40

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Donor's "Name": Nova

Year of Birth: 1999

Marital Status: Single

Number of Children: 0

Occupation:
(last reported) Student

Education: Bachelor, Mechanical Engineering, Bachelor, Finance

Blood Type: O +

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

Race: Hispanic Or Latino

CMV Status: NEG
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Last Medical History Update: 02/05/2024

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

  • Height:
    5'8" (172.72 cm)
    Weight:
    145 lbs (65 kg)
    Eye Color:
    Brown, Dark
    Hair Color:
    Black
    Hair Texture:
    Thick
    Hair Loss:
    None
    Hair Type:
    Curly
    Dominant Hand:
    Right
    Hairy Chest:
    No
    Hairy:
    No
    Ear Lobes:
    Attached
    Beard Color:
    Black
    Eyebrows:
    Medium
    Dimples:
    No
    Acne:
    No
    Acne Information:
    Shoe Size:
    11
    Body Build:
    Medium
    Freckles:
    None
    Skin Tone:
    Brown, Light
    Face Shape:
    Oval
    Lips:
    Thick
    Nose Shape:
    Roman
    Long Eyelashes:
    Yes

  • I immigrated to the United States when I was roughly two years old. I would move various times over the years due to my dad’s occupation. As a result, I’ve lived in about seven states and three countries. The consistent moving around meant that my family became very tight-knit and my older sister and I became very comfortable being in new environments and meeting different people. I was very fortunate growing up, and the experiences I was able to have molded me into the person that I am.
    I’m not a particularly shy person, since I would constantly meet new people from a very young age. Because of this, I am typically very direct with just about anyone. Coupling this directness with my rather dry humor, some people may get the incorrect impression that I’m rude. It’s never my intention to upset anyone, but if there’s something I greatly dislike its people who aren’t straightforward, hence my insistence on being as direct as possible. I mean what I say when I say it, and I appreciate it when people reciprocate that mindset. In all aspects of life, I tend to prefer the quickest and most direct routes. This goes for conversations, traveling, and anything in between. Due to this general mindset, I can be somewhat impatient, and I generally dislike small talk and slow walkers. I like high-energy and passionate people. I think it’s fantastic when someone can describe what they’re passionate about in vivid detail and show that they’re actively working to improve and refine what it is that they’re passionate about.
    In terms of hobbies, I greatly enjoy playing tennis, working out, binging YouTube, and working on hands-on projects. I’m passionate about anything that moves, whether it’s a car, a plane, or anything along those lines. In my free time, I like working on personal projects that I know will result in a tangible item, such as an RC plane or model car. I’m currently working towards completing my bachelor’s degree in mechanical engineering and so far, I’m enjoying it a lot. In school, I’m able to work on designing and creating physical products that I’m able to hold and use in the end.
    Some advice I might give is that none of us should be too concerned with how others choose to perceive us. Everyone’s entitled to their opinion, but no one is entitled to my time. Another big one would be that it’s never too late to start something, whether it’s school or just a hobby. On that note, no one should feel discouraged if they initially struggle to grasp something that’s new to them. Things take time, and persistence and effort are always key to accomplishing one’s goals.

    Sincerely,
    Donor 92107

  • ADVISORY

    This donor is a carrier of one or more genetic conditions.

    The list below includes the condition(s) that the donor carries. To view a complete list of the genes included in the donor's carrier testing click the relevant link below. To download the donor's test reports click the relevant link below. To purchase this donor's sperm, the intended parent/recipient must sign an acknowledgement form. For more information, please contact us.

    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 301 genes.

    Cartilage-Hair Hypoplasia (RMRP)
    Carrier
    Schimke Immunoosseous Dysplasia (SMARCAL1)
    Carrier
    21-Alpha-Hydroxylase-Deficient Congenital Adrenal Hyperplasia (CYP21A2)
    No disease-causing mutations detected
    3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (HMGCL)
    No disease-causing mutations detected
    3-Methylcrotonyl-CoA Carboxylase Deficiency, MCCC1-Related (MCCC1)
    No disease-causing mutations detected
    3-Methylcrotonyl-CoA Carboxylase Deficiency, MCCC2-Related (MCCC2)
    No disease-causing mutations detected
    3-Methylglutaconic Aciduria Type III also known as Costeff Optic Atrophy (OPA3)
    No disease-causing mutations detected
    3-Phosphoglycerate Dehydrogenase Deficiency, PHGDH-Related (PHGDH)
    No disease-causing mutations detected
    6-Pyruvoyl-Tetrahydropterin Synthase Deficiency (PTS)
    No disease-causing mutations detected
    Abetalipoproteinemia (MTTP)
    No disease-causing mutations detected
    Achromatopsia (CNGB3)
    No disease-causing mutations detected
    Acrodermatitis Enteropathica (SLC39A4)
    No disease-causing mutations detected
    Acute Infantile Liver Failure (TRMU)
    No disease-causing mutations detected
    Acyl-CoA Oxidase I Deficiency (ACOX1)
    No disease-causing mutations detected
    Adenosine Deaminase Deficiency (ADA)
    No disease-causing mutations detected
    Adrenoleukodystrophy, X-Linked (ABCD1)
    No disease-causing mutations detected
    Aicardi-Goutieres Syndrome (SAMHD1)
    No disease-causing mutations detected
    Aldosterone Synthase Deficiency also known as Corticosterone Methyloxidase Deficiency (CYP11B2)
    No disease-causing mutations detected
    Alkaptonuria (HGD)
    No disease-causing mutations detected
    Alpha-1 Antitrypsin Deficiency (SERPINA1)
    No disease-causing mutations detected
    Alpha-Mannosidosis (MAN2B1)
    No disease-causing mutations detected
    Alpha-Thalassemia (HBA1/HBA2)
    No disease-causing mutations detected; normal hemoglobin analysis
    Alpha-Thalassemia Intellectual Disability Syndrome, X-Linked (ATRX)
    No disease-causing mutations detected
    Alport Syndrome, COL4A3-Related (COL4A3)
    No disease-causing mutations detected
    Alport Syndrome, COL4A4-Related (COL4A4)
    No disease-causing mutations detected
    Alport Syndrome, X-Linked (COL4A5)
    No disease-causing mutations detected
    Alstrom Syndrome (ALMS1)
    No disease-causing mutations detected
    Andermann Syndrome (SLC12A6)
    No disease-causing mutations detected
    Arginase Deficiency also known as Argininemia (ARG1)
    No disease-causing mutations detected
    Argininosuccinic Aciduria (ASL)
    No disease-causing mutations detected
    Aromatase Deficiency (CYP19A1)
    No disease-causing mutations detected
    Arthrogryposis, Mental Retardation, and Seizures (SLC35A3)
    No disease-causing mutations detected
    Asparagine Synthetase Deficiency (ASNS)
    No disease-causing mutations detected
    Aspartylglucosaminuria (AGA)
    No disease-causing mutations detected
    Ataxia With Vitamin E Deficiency (TTPA)
    No disease-causing mutations detected
    Ataxia-Telangiectasia (ATM)
    No disease-causing mutations detected
    Bardet-Biedl Syndrome, BBS1-Related (BBS1)
    No disease-causing mutations detected
    Bardet-Biedl Syndrome, BBS10-Related (BBS10)
    No disease-causing mutations detected
    Bardet-Biedl Syndrome, BBS12-Related (BBS12)
    No disease-causing mutations detected
    Bardet-Biedl Syndrome, BBS2-Related (BBS2)
    No disease-causing mutations detected
    Bartter Syndrome, Type 4A (BSND)
    No disease-causing mutations detected
    Bernard-Soulier Syndrome, Type A1 (GP1BA)
    No disease-causing mutations detected
    Bernard-Soulier Syndrome, Type C (GP9)
    No disease-causing mutations detected
    Beta-Ketothiolase Deficiency (ACAT1)
    No disease-causing mutations detected
    Beta-Thalassemia, Sickle Cell Disease, and Beta-Globin Disorders (HBB)
    No disease-causing mutations detected; normal hemoglobin analysis
    Biotinidase Deficiency (BTD)
    No disease-causing mutations detected
    Bloom Syndrome (BLM)
    No disease-causing mutations detected
    Canavan Disease (ASPA)
    No disease-causing mutations detected
    Carbamoylphosphate Synthetase I Deficiency (CPS1)
    No disease-causing mutations detected
    Carnitine Palmitoyltransferase IA Deficiency (CPT1A)
    No disease-causing mutations detected
    Carnitine Palmitoyltransferase II Deficiency (CPT2)
    No disease-causing mutations detected
    Carpenter Syndrome (RAB23)
    No disease-causing mutations detected
    Cerebral Creatine Deficiency Syndrome 1, X-Linked (SLC6A8)
    No disease-causing mutations detected
    Cerebrotendinous Xanthomatosis (CYP27A1)
    No disease-causing mutations detected
    Charcot-Marie-Tooth Disease, Type 4D (NDRG1)
    No disease-causing mutations detected
    Charcot-Marie-Tooth Disease, Type 5 / Arts Syndrome, X-Linked (PRPS1)
    No disease-causing mutations detected
    Charcot-Marie-Tooth Disease, X-Linked (GJB1)
    No disease-causing mutations detected
    Choreoacanthocytosis (VPS13A)
    No disease-causing mutations detected
    Choroidemia, X-Linked (CHM)
    No disease-causing mutations detected
    Chromosome Analysis (Karyotype)
    Normal male karyotype
    Chronic Granulomatous Disease, CYBA-Related (CYBA)
    No disease-causing mutations detected
    Chronic Granulomatous Disease, CYBB-Related, X-Linked (CYBB)
    No disease-causing mutations detected
    Citrin Deficiency (SLC25A13)
    No disease-causing mutations detected
    Citrullinemia Type 1 (ASS1)
    No disease-causing mutations detected
    Cockayne Syndrome Type A (ERCC8)
    No disease-causing mutations detected
    Cockayne Syndrome Type B (ERCC6)
    No disease-causing mutations detected
    Cohen Syndrome (VPS13B)
    No disease-causing mutations detected
    Combined Malonic and Methylmalonic Aciduria (ACSF3)
    No disease-causing mutations detected
    Combined Oxidative Phosphorylation Deficiency 1 (GFM1)
    No disease-causing mutations detected
    Combined Oxidative Phosphorylation Deficiency 3 (TSFM)
    No disease-causing mutations detected
    Combined Pituitary Hormone Deficiency 2 (PROP1)
    No disease-causing mutations detected
    Combined Pituitary Hormone Deficiency 3 (LHX3)
    No disease-causing mutations detected
    Combined SAP Deficiency (PSAP)
    No disease-causing mutations detected
    Congenital Adrenal Hyperplasia due to 11-Beta-Hydroxylase Deficiency (CYP11B1)
    No disease-causing mutations detected
    Congenital Adrenal Hyperplasia due to 17-Alpha-Hydroxylase Deficiency (CYP17A1)
    No disease-causing mutations detected
    Congenital Adrenal Hyperplasia due to 3-Beta-Hydroxysteroid Dehydrogenase Type II Deficiency (HSD3B2)
    No disease-causing mutations detected
    Congenital Amegakaryocytic Thrombocytopenia (MPL)
    No disease-causing mutations detected
    Congenital Disorder of Glycosylation Type 1a, PMM2-Related (PMM2)
    No disease-causing mutations detected
    Congenital Disorder of Glycosylation Type 1b (MPI)
    No disease-causing mutations detected
    Congenital Disorder of Glycosylation, Type Ic (ALG6)
    No disease-causing mutations detected
    Congenital Insensitivity to Pain with Anhidrosis (NTRK1)
    No disease-causing mutations detected
    Congenital Myasthenic Syndrome (CHRNE)
    No disease-causing mutations detected
    Congenital Myasthenic Syndrome (RAPSN)
    No disease-causing mutations detected
    Congenital Neutropenia (HAX1)
    No disease-causing mutations detected
    Congenital Neutropenia, VPS45-Related (VPS45)
    No disease-causing mutations detected
    Corneal Dystrophy and Perceptive Deafness (SLC4A11)
    No disease-causing mutations detected
    Cystic Fibrosis and Other CFTR-Related Disorders (CFTR)
    No disease-causing mutations detected
    Cystinosis (CTNS)
    No disease-causing mutations detected
    D-Bifunctional Protein Deficiency (HSD17B4)
    No disease-causing mutations detected
    Deafness, Autosomal Recessive 77 (LOXHD1)
    No disease-causing mutations detected
    Dyskeratosis Congenita, RTEL1-Related (RTEL1)
    No disease-causing mutations detected
    Dystrophic Epidermolysis Bullosa (COL7A1)
    No disease-causing mutations detected
    Dystrophinopathies, DMD-Related, X-Linked (DMD)
    No disease-causing mutations detected
    Ehlers-Danlos Syndrome, Type VIIC (ADAMTS2)
    No disease-causing mutations detected
    Ellis-Van Creveld Syndrome, EVC-Related (EVC)
    No disease-causing mutations detected
    Ellis-Van Creveld Syndrome, EVC2-Related (EVC2)
    No disease-causing mutations detected
    Emery-Dreifuss Muscular Dystrophy, X-Linked (EMD)
    No disease-causing mutations detected
    Enhanced S-Cone Syndrome (NR2E3)
    No disease-causing mutations detected
    Ethylmalonic Encephalopathy (ETHE1)
    No disease-causing mutations detected
    F5-Related Disorders (F5)
    No disease-causing mutations detected
    Fabry Disease, X-Linked (GLA)
    No disease-causing mutations detected
    Factor IX Deficiency, X-Linked (F9)
    No disease-causing mutations detected
    Factor XI Deficiency (F11)
    No disease-causing mutations detected
    Familial Dysautonomia (ELP1)
    No disease-causing mutations detected
    Familial Hypercholesterolemia (LDLR)
    No disease-causing mutations detected
    Familial Hypercholesterolemia (LDLRAP1)
    No disease-causing mutations detected
    Familial Hyperinsulinism and Other ABCC8-Related Disorders (ABCC8)
    No disease-causing mutations detected
    Familial Hyperinsulinism and Other KCNJ11-Related Disorders (KCNJ11)
    No disease-causing mutations detected
    Familial Mediterranean Fever (MEFV)
    No disease-causing mutations detected
    Fanconi Anemia Type A (FANCA)
    No disease-causing mutations detected
    Fanconi Anemia Type C (FANCC)
    No disease-causing mutations detected
    Fanconi Anemia, Type G (FANCG)
    No disease-causing mutations detected
    FKTN-Related Disorders including Walker-Warburg Syndrome (FKTN)
    No disease-causing mutations detected
    Fragile X Syndrome (FMR1)
    No disease-causing mutations detected; CGG repeat number within normal range
    Fumarase Deficiency (FH)
    No disease-causing mutations detected
    Galactokinase Deficiency (GALK1)
    No disease-causing mutations detected
    Galactosemia, GALT-Related (GALT)
    No disease-causing mutations detected
    Gaucher Disease (GBA)
    No disease-causing mutations detected
    Gitelman Syndrome (SLC12A3)
    No disease-causing mutations detected
    GJB2-Related DFNB1 Nonsyndromic Hearing Loss and Deafness (GJB2)
    No disease-causing mutations detected
    Glucose-6-Phosphate Dehydrogenase Deficiency, X-Linked (G6PD)
    No disease-causing mutations detected
    Glutaric Acidemia Type 1 (GCDH)
    No disease-causing mutations detected
    Glutaric Acidemia, Type IIa (ETFA)
    No disease-causing mutations detected
    Glutaric Acidemia, Type IIc (ETFDH)
    No disease-causing mutations detected
    Glycine Encephalopathy, AMT-Related (AMT)
    No disease-causing mutations detected
    Glycine Encephalopathy, GLDC-Related (GLDC)
    No disease-causing mutations detected
    Glycogen Storage Disease Type Ia (G6PC)
    No disease-causing mutations detected
    Glycogen Storage Disease Type Ib (SLC37A4)
    No disease-causing mutations detected
    Glycogen Storage Disease Type III (AGL)
    No disease-causing mutations detected
    Glycogen Storage Disease Type V (PYGM)
    No disease-causing mutations detected
    Glycogen Storage Disease, Type IV also known as Adult Polyglucosan Body Disease (GBE1)
    No disease-causing mutations detected
    Glycogen Storage Disease, Type VII (PFKM)
    No disease-causing mutations detected
    GRACILE Syndrome (BCS1L)
    No disease-causing mutations detected
    Guanidinoacetate Methyltransferase Deficiency also known as Cerebral Creatine Deficiency Syndrome 2 (GAMT)
    No disease-causing mutations detected
    Hemochromatosis, Type 3 (TFR2)
    No disease-causing mutations detected
    Hereditary Fructose Intolerance (ALDOB)
    No disease-causing mutations detected
    Hereditary Hemochromatosis (HJV)
    No disease-causing mutations detected
    Hereditary Hemochromatosis Type 1 (HFE)
    No disease-causing mutations detected
    Hereditary Spastic Paraparesis 49 (TECPR2)
    No disease-causing mutations detected
    Hermansky-Pudlak Syndrome, Type 1 (HPS1)
    No disease-causing mutations detected
    Hermansky-Pudlak Syndrome, Type 3 (HPS3)
    No disease-causing mutations detected
    Holocarboxylase Synthetase Deficiency (HLCS)
    No disease-causing mutations detected
    Homocystinuria (CBS)
    No disease-causing mutations detected
    Homocystinuria due to MTHFR Deficiency (MTHFR)
    No disease-causing mutations detected
    Homocystinuria, Cobalamin E Type (MTRR)
    No disease-causing mutations detected
    Hydrolethalus Syndrome (HYLS1)
    No disease-causing mutations detected
    Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome (SLC25A15)
    No disease-causing mutations detected
    Hypohidrotic Ectodermal Dysplasia, X-Linked (EDA)
    No disease-causing mutations detected
    Hypophosphatasia, Autosomal Recessive (ALPL)
    No disease-causing mutations detected
    Inclusion Body Myopathy 2 (GNE)
    No disease-causing mutations detected
    Isovaleric Acidemia (IVD)
    No disease-causing mutations detected
    Joubert Syndrome 2 (TMEM216)
    No disease-causing mutations detected
    Joubert Syndrome 7 also known as Meckel Syndrome 5 (RPGRIP1L)
    No disease-causing mutations detected
    Junctional Epidermolysis Bullosa (LAMA3)
    No disease-causing mutations detected
    Junctional Epidermolysis Bullosa (LAMB3)
    No disease-causing mutations detected
    Junctional Epidermolysis Bullosa (LAMC2)
    No disease-causing mutations detected
    Juvenile Retinoschisis, X-Linked (RS1)
    No disease-causing mutations detected
    Krabbe Disease (GALC)
    No disease-causing mutations detected
    Leber Congenital Amaurosis 10 and Other CEP290-Related Ciliopathies (CEP290)
    No disease-causing mutations detected
    Leber Congenital Amaurosis 13 (RDH12)
    No disease-causing mutations detected
    Leber Congenital Amaurosis 2 also known as Retinitis Pigmentosa 20 (RPE65)
    No disease-causing mutations detected
    Leber Congenital Amaurosis 5 (LCA5)
    No disease-causing mutations detected
    Leber Congenital Amaurosis 8 also known as Retinitis Pigmentosa 12 (CRB1)
    No disease-causing mutations detected
    Leigh Syndrome, French-Canadian Type (LRPPRC)
    No disease-causing mutations detected
    Lethal Congenital Contracture Syndrome 1 (GLE1)
    No disease-causing mutations detected
    Limb-Girdle Muscular Dystrophy Type 2A also known as Calpainopathy (CAPN3)
    No disease-causing mutations detected
    Limb-Girdle Muscular Dystrophy Type 2B also known as Dysferlinopathy (DYSF)
    No disease-causing mutations detected
    Limb-Girdle Muscular Dystrophy Type 2C also known as Gamma-Sarcoglycanopathy (SGCG)
    No disease-causing mutations detected
    Limb-Girdle Muscular Dystrophy Type 2D also known as Alpha-Sarcoglycanopathy (SGCA)
    No disease-causing mutations detected
    Limb-Girdle Muscular Dystrophy Type 2E also known as Beta-Sarcoglycanopathy (SGCB)
    No disease-causing mutations detected
    Limb-Girdle Muscular Dystrophy Type 2I (FKRP)
    No disease-causing mutations detected
    Lipoid Adrenal Hyperplasia (STAR)
    No disease-causing mutations detected
    Lipoprotein Lipase Deficiency (LPL)
    No disease-causing mutations detected
    Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (HADHA)
    No disease-causing mutations detected
    Lysinuric Protein Intolerance (SLC7A7)
    No disease-causing mutations detected
    Lysosomal Acid Lipase Deficiency including Wolman Disease and Cholesteryl Ester Storage Disease (LIPA)
    No disease-causing mutations detected
    Major Histocompatibility Complex Class II Deficiency also known as Bare Lymphocyte Syndrome Type II (CIITA)
    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 2 (DBT)
    No disease-causing mutations detected
    Maple Syrup Urine Disease Type 3 also known as Dihyrolipoamide Dehydrogenase Deficiency (DLD)
    No disease-causing mutations detected
    Medium Chain Acyl-CoA Dehydrogenase Deficiency (ACADM)
    No disease-causing mutations detected
    Megalencephalic Leukoencephalopathy With Subcortical Cysts Type 1 (MLC1)
    No disease-causing mutations detected
    Menkes Disease and Other ATP7A-Related Disorders, X-Linked (ATP7A)
    No disease-causing mutations detected
    Merosin-Deficient Muscular Dystrophy (LAMA2)
    No disease-causing mutations detected
    Metachromatic Leukodystrophy (ARSA)
    No disease-causing mutations detected
    Methylmalonic Acidemia (MMAA)
    No disease-causing mutations detected
    Methylmalonic Acidemia (MMAB)
    No disease-causing mutations detected
    Methylmalonic Acidemia (MUT)
    No disease-causing mutations detected
    Methylmalonic Aciduria and Homocystinuria, Cobalamin C Type (MMACHC)
    No disease-causing mutations detected
    Methylmalonic Aciduria and Homocystinuria, Cobalamin D Type (MMADHC)
    No disease-causing mutations detected
    Microphthalmia and Anophthalmia (VSX2)
    No disease-causing mutations detected
    Mitochondrial Complex I Deficiency (ACAD9)
    No disease-causing mutations detected
    Mitochondrial Complex I Deficiency 16 (NDUFAF5)
    No disease-causing mutations detected
    Mitochondrial Complex I Deficiency, NDUFS6-Related (NDUFS6)
    No disease-causing mutations detected
    Mitochondrial DNA Depletion Syndrome 6 also known as Navajo Neurohepatopathy (MPV17)
    No disease-causing mutations detected
    Mitochondrial Myopathy and Sideroblastic Anemia 1 (PUS1)
    No disease-causing mutations detected
    Mitochondrial Neurogastrointestinal Encephalopathy Disease (TYMP)
    No disease-causing mutations detected
    MKS1-Related Disorders, including Bardet-Biedl Syndrome 13, Joubert Syndrome 28, and Meckel Syndrome 1 (MKS1)
    No disease-causing mutations detected
    Mucolipidosis II and IIIA (GNPTAB)
    No disease-causing mutations detected
    Mucolipidosis III Gamma (GNPTG)
    No disease-causing mutations detected
    Mucolipidosis Type IV (MCOLN1)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type I also known as Hurler Syndrome (IDUA)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type II also known as Hunter Syndrome, X-Linked (IDS)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type IIIA also known as Sanfilippo A Syndrome (SGSH)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type IIIB also known as Sanfilippo B Syndrome (NAGLU)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type IIIC also known as Sanfilippo C Syndrome (HGSNAT)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type IIID (GNS)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type IVb also known as GM1 Gangliosidosis (GLB1)
    No disease-causing mutations detected
    Mucopolysaccharidosis Type VI (ARSB)
    No disease-causing mutations detected
    Mucopolysaccharidosistype IX (HYAL1)
    No disease-causing mutations detected
    Multiple Sulphatase Deficiency (SUMF1)
    No disease-causing mutations detected
    Muscle-Eye-Brain Disease (POMGNT1)
    No disease-causing mutations detected
    Myotubular Myopathy, X-Linked (MTM1)
    No disease-causing mutations detected
    N-Acetylglutamate Synthase Deficiency (NAGS)
    No disease-causing mutations detected
    Nemaline Myopathy 2 (NEB)
    No disease-causing mutations detected
    Nephrogenic Diabetes Insipidus, Type II (AQP2)
    No disease-causing mutations detected
    Nephrotic Syndrome, NPHS1-Related also known as Congenital Finnish Nephrosis (NPHS1)
    No disease-causing mutations detected
    Nephrotic Syndrome, NPHS2-Related also known as Steroid-Resistant Nephrotic Syndrome (NPHS2)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, CLN3-Related (CLN3)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, CLN5-Related (CLN5)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, CLN6-Related (CLN6)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, CLN8-Related also known as Northern Epilepsy (CLN8)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, MFSD8-Related (MFSD8)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, PPT1-Related (PPT1)
    No disease-causing mutations detected
    Neuronal Ceroid-Lipofuscinosis, TPP1-Related (TPP1)
    No disease-causing mutations detected
    Niemann-Pick Disease Type A/B (SMPD1)
    No disease-causing mutations detected
    Niemann-Pick Disease Type C, NPC1-Related (NPC1)
    No disease-causing mutations detected
    Niemann-Pick Disease Type C, NPC2-Related (NPC2)
    No disease-causing mutations detected
    Nijmegen Breakage Syndrome (NBN)
    No disease-causing mutations detected
    Odonto-Onycho-Dermal Dysplasia also known as Schopf-Schulz-Passarge Syndrome (WNT10A)
    No disease-causing mutations detected
    Omenn Syndrome and Severe Combined Immunodeficiency, Athabaskan-Type (DCLRE1C)
    No disease-causing mutations detected
    Omenn Syndrome, RAG2-Related (RAG2)
    No disease-causing mutations detected
    Ornithine Aminotransferase Deficiency (OAT)
    No disease-causing mutations detected
    Ornithine Transcarbamylase Deficiency, X-Linked (OTC)
    No disease-causing mutations detected
    Osteochondrodysplasias, Sulfate Transporter-Related (SLC26A2)
    No disease-causing mutations detected
    Osteopetrosis Type 1 (TCIRG1)
    No disease-causing mutations detected
    Pendred Syndrome (SLC26A4)
    No disease-causing mutations detected
    Peroxisome Biogenesis Disorder, Type 3 (PEX12)
    No disease-causing mutations detected
    Phenylalanine Hydroxylase Deficiency also known as Phenylketonuria (PAH)
    No disease-causing mutations detected
    Polycystic Kidney Disease, Autosomal Recessive (PKHD1)
    No disease-causing mutations detected
    Polyglandular Autoimmune Syndrome Type 1 (AIRE)
    No disease-causing mutations detected
    Polymicrogyria (ADGRG1)
    No disease-causing mutations detected
    Pompe Disease also known as Glycogen Storage Disease Type II (GAA)
    No disease-causing mutations detected
    Pontocerebellar Hypoplasia Type 1A (VRK1)
    No disease-causing mutations detected
    Pontocerebellar Hypoplasia Type 6 (RARS2)
    No disease-causing mutations detected
    Postnatal Progressive Microcephaly also known as Infantile Cerebral and Cerebellar Atrophy (MED17)
    No disease-causing mutations detected
    Primary Carnitine Deficiency (SLC22A5)
    No disease-causing mutations detected
    Primary Ciliary Dyskinesia, DNAH5-Related (DNAH5)
    No disease-causing mutations detected
    Primary Ciliary Dyskinesia, DNAI1-Related (DNAI1)
    No disease-causing mutations detected
    Primary Ciliary Dyskinesia, DNAI2-Related (DNAI2)
    No disease-causing mutations detected
    Primary Hyperoxaluria Type 1 (AGXT)
    No disease-causing mutations detected
    Primary Hyperoxaluria Type 2 (GRHPR)
    No disease-causing mutations detected
    Primary Hyperoxaluria, Type 3 (HOGA1)
    No disease-causing mutations detected
    Progressive Cerebello-Cerebral Atrophy (SEPSECS)
    No disease-causing mutations detected
    Progressive Familial Intrahepatic Cholestasis Type 2 (ABCB11)
    No disease-causing mutations detected
    Propionic Acidemia, PCCA-Related (PCCA)
    No disease-causing mutations detected
    Propionic Acidemia, PCCB-Related (PCCB)
    No disease-causing mutations detected
    Prothrombin-Related Thrombophilia (F2)
    No disease-causing mutations detected
    Pycnodysostosis (CTSK)
    No disease-causing mutations detected
    Pyruvate Carboxylase Deficiency (PC)
    No disease-causing mutations detected
    Pyruvate Dehydrogenase E1-Alpha Deficiency, X-Linked (PDHA1)
    No disease-causing mutations detected
    Pyruvate Dehydrogenase E1-Beta Deficiency (PDHB)
    No disease-causing mutations detected
    Renal Tubular Acidosis and Deafness (ATP6V1B1)
    No disease-causing mutations detected
    Retinitis Pigmentosa 25 (EYS)
    No disease-causing mutations detected
    Retinitis Pigmentosa 26 (CERKL)
    No disease-causing mutations detected
    Retinitis Pigmentosa 28 (FAM161A)
    No disease-causing mutations detected
    Retinitis Pigmentosa 59 (DHDDS)
    No disease-causing mutations detected
    Rhizomelic Chondrodysplasia Punctata Type 1 (PEX7)
    No disease-causing mutations detected
    Rhizomelic Chondrodysplasia Punctata Type 3 (AGPS)
    No disease-causing mutations detected
    Roberts Syndrome (ESCO2)
    No disease-causing mutations detected
    Salla Disease (SLC17A5)
    No disease-causing mutations detected
    Sandhoff Disease (HEXB)
    No disease-causing mutations detected
    Severe Combined Immunodeficiency, X-Linked (IL2RG)
    No disease-causing mutations detected
    Sjogren-Larsson Syndrome (ALDH3A2)
    No disease-causing mutations detected
    Smith-Lemli-Opitz Syndrome (DHCR7)
    No disease-causing mutations detected
    Spastic Ataxia of Charlevoix-Saguenay, Autosomal Recessive (SACS)
    No disease-causing mutations detected
    Spastic Paraplegia, Type 15 (ZFYVE26)
    No disease-causing mutations detected
    Spinal Muscular Atrophy (SMN1)
    No disease-causing mutations detected (2 copies detected)
    Spondylothoracic Dysostosis (MESP2)
    No disease-causing mutations detected
    Steel Syndrome (COL27A1)
    No disease-causing mutations detected
    Stuve-Wiedemann Syndrome (LIFR)
    No disease-causing mutations detected
    Tay-Sachs Disease also known as Hexosaminidase A Deficiency (HEXA)
    No disease-causing mutations detected
    TGM1-Related Autosomal Recessive Congenital Ichthyosis (TGM1)
    No disease-causing mutations detected
    Tyrosine Hydroxylase Deficiency (TH)
    No disease-causing mutations detected
    Tyrosinemia Type 1 (FAH)
    No disease-causing mutations detected
    Tyrosinemia, Type II (TAT)
    No disease-causing mutations detected
    Usher Syndrome Type IB (MYO7A)
    No disease-causing mutations detected
    Usher Syndrome Type IC (USH1C)
    No disease-causing mutations detected
    Usher Syndrome Type ID (CDH23)
    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
    Vanishing White Matter Disease (EIF2B5)
    No disease-causing mutations detected
    Very Long Chain Acyl-CoA Dehydrogenase Deficiency (ACADVL)
    No disease-causing mutations detected
    Wilson Disease (ATP7B)
    No disease-causing mutations detected
    Xeroderma Pigmentosum, Group A (XPA)
    No disease-causing mutations detected
    Xeroderma Pigmentosum, Group C (XPC)
    No disease-causing mutations detected
    Zellweger Spectrum Disorder, PEX2-Related (PEX2)
    No disease-causing mutations detected
    Zellweger Spectrum Disorder, PEX6-Related (PEX6)
    No disease-causing mutations detected
    Zellweger Syndrome Spectrum (PEX1)
    No disease-causing mutations detected
    Zellweger Syndrome Spectrum, PEX10- Related (PEX10)
    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:
    Yes
    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:
    Yes
    Stomach Ulcers:
    No

  • ATHLETIC

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    COUCH POTATO

    OPTIMISTIC

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    PESSIMISTIC

    ASSERTIVE

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    PASSIVE

    LEADER

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    FOLLOWER

    EASY GOING

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    CONTROLLING, RIGID

    ARTISTIC

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    MICHELANGELO WHO?

    EXTROVERT

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    INTROVERT

    Celebrity Look Alike:

    Vegetarian: No

    Adjectives: Persistent, Adaptive, Observant

    Fine Art Skills: Played alto saxophone for 3 years

    Technical/Mechanical Ability: Solid works, AutoCAD, proficient with power tools, woodworking, MATLAB, Python, MS Suite, etc.

    Skills, Hobbies and Interests: I studied finance and mechanical engineering in school, so I'm decent with math, accounting, physical sciences, computer-aided design. I love to cook, play tennis, read, and watch movies in my spare time. I speak Spanish and Portuguese with some proficiency.

  • Carried to Term:
    No
    Pregnancy Complications:
    No
    Birth Weight:
    4 lbs ounces
    Childhood Health:
    Good
    Birth Length:
    12 inches
    Twin:
    No
    Twin Type:
    In School:
    Yes
    Is the donor currently enrolled in or does the donor hold an undergraduate degree?
    Yes
    Degree Earned/Working towards:
    Bachelor
    Degree Status:
    Currently enrolled
    Major:
    Mechanical Engineering
    Minor:
    None
    Degree Earned/Working towards:
    Bachelor
    Degree Status:
    Currently enrolled
    Major:
    Finance
    Minor:
    None
    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.)?
    No

  • 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 Great Grandmother X 90
    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
    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 Mother 5
    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) Dust mites X Mother 5
    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: Fair Dominant Hand:
    Year of Birth: 1972 Cause of Death: Hair Loss:
    Height: 5'10" (177.8 cm) Age at Death: Body Hair: Straight
    Weight: 170 lbs. (77 kg) Occupation: Military 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. Fluent in Spanish. Enjoys playing soccer.
    FAMILY MEMBER: Mother
    Hair Color: Black Eyesight:
    Freckles: None Hair Texture:
    Health Status: Good Skin Tone: Fair Dominant Hand:
    Year of Birth: 1973 Cause of Death: Hair Loss:
    Height: 5'03" (160.02 cm) Age at Death: Body Hair: Straight
    Weight: 130 lbs. (59 kg) Occupation: State Department, Retired Eye Color: Black
    Half Siblings: No Education: College Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision. Always eager to start some new business venture or craft. Fluent in Spanish & Portuguese. Loves bad horror movies.
    FAMILY MEMBER: Sister
    Hair Color: Brown, Dark Eyesight:
    Freckles: None Hair Texture:
    Health Status: Good Skin Tone: Medium Dominant Hand:
    Year of Birth: 1996 Cause of Death: Hair Loss:
    Height: 5'04" (162.56 cm) Age at Death: Body Hair: Straight
    Weight: 140 lbs. (63 kg) Occupation: 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 and a slight Roman nose. Gets a new hobby every week. Skilled in coding (software engineering). Fluent in Spanish and proficient in Portuguese. Owns a toy poodle (Sgt. Pepper).

  • 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: Olive Dominant Hand:
    Year of Birth: 1946 Cause of Death: Hair Loss:
    Height: 5'10" (177.8 cm) Age at Death: Body Hair: Straight
    Weight: 160 lbs. (72 kg) Occupation: Sales Eye Color: Black
    Half Siblings: Education: College (Some) Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision.
    FAMILY MEMBER: Grandmother
    Hair Color: Black Eyesight:
    Freckles: None Hair Texture:
    Health Status: Good Skin Tone: Fair Dominant Hand:
    Year of Birth: 1947 Cause of Death: Hair Loss:
    Height: 5'" (152.4 cm) Age at Death: Body Hair: Straight
    Weight: 135 lbs. (61 kg) Occupation: Hairdresser Eye Color: Black
    Half Siblings: Education: High School Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision. Good hair stylist.
    FAMILY MEMBER: Uncle
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1975 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:

  • 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: Skin Tone: Brown, Medium Dominant Hand:
    Year of Birth: 1928 Cause of Death: Old age Hair Loss:
    Height: 5'04" (162.56 cm) Age at Death: 92 Body Hair: Curly
    Weight: 140 lbs. (63 kg) Occupation: Shoe Factory Owner Eye Color: Blue
    Half Siblings: Education: High School Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Had corrected vision and a Roman nose. Fled Spain with his mother. Enjoyed leather working, shoe design, and reading.
    FAMILY MEMBER: Grandmother
    Hair Color: Black Eyesight:
    Freckles: None Hair Texture:
    Health Status: Good Skin Tone: Brown, Light Dominant Hand:
    Year of Birth: 1951 Cause of Death: Hair Loss:
    Height: 5'" (152.4 cm) Age at Death: Body Hair: Straight
    Weight: 130 lbs. (59 kg) Occupation: Eye Color: Black
    Half Siblings: Education: High School Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision. Raised as an orphan by nuns. Enjoys watching Telenovelas.
    FAMILY MEMBER: Uncle
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1982 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:
Buy 2 get 1 complimentary on this featured donor

Purchase Bundle Options

Purchase Bundle Options

Vial Types Available for Donor #92107

All prices shown are in USD.

$1495 per vial Identity Disclosure xyGene Washed

$1495 per vial Identity Disclosure xyGene Unwashed

$1250 per vial Identity Disclosure xyGene ART

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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