Meet Tristan (9607) – Open ID Donor.

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Tristan is incredibly attractive and we can see why he works as a model. He has a chiseled jaw with a tiny cleft in the center of the chin. He has full red lips and a big smile. Tristan could easily rock the surfer look with his sandy blonde hair, big blue eyes, and naturally tanned skin. Tristan is very active and has the muscular physique to keep up with his many activities. He is typically seen in workout clothes or trendy sports clothes.

This donor is very intelligent and witty. He is currently enrolled in a top university to finish his psychology degree. Tristan loves to meet new people and is naturally gregarious. He is also charming and sweet. Tristan is a musician and plays the guitar and piano. He is very well rounded and we think he would make a fabulous genetic donor to your family.


Genetic Testing

Over the years, we have expanded our 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. All donors have undergone genetic testing for Cystic Fibrosis, Spinal Muscular Atrophy and Karyotyping.  However, many donors have had more extensive testing performed.

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.

Since this donor is a carrier for 1 or more conditions, we require that you fill out the Informed Consent document found HERE
This consent form needs to be completed and sent to us, prior to shipment.

Karyotyping  Normal Male Karyoptype, 46XY
adenosine deaminase deficiency Non-Carrier
alpha-mannosidosis Non-Carrier
Anderman syndrome Non-Carrier
argininosuccinic aciduria Non-Carrier
aspartylglucosaminuria Non-Carrier
ataxia-telangiectasia Non-Carrier
ARSACS Non-Carrier
Bardet-Biedl syndrome, BBS1-related Non-Carrier
Bardet-Biedl syndrome, BBS10-related Carrier
beta hemoglobinopathy, beta thalassemia Non-Carrier
beta hemoglobinopathy, sickle cell disease Non-Carrier
beta hemoglobinopathies, hemoglobins C, D, E, and O Non-Carrier
Bloom syndrome Non-Carrier
Canavan disease Non-Carrier
cartilage-hair hypoplasia Non-Carrier
citrullinemia type 1 Non-Carrier
cobalamin C disease Non-Carrier
congenital disorder of glycosylation type 1a Non-Carrier
congenital Finnish nephrosis Non-Carrier
cystic fibrosis Non-Carrier
cystinosis Non-Carrier
D-bifunctional protein deficiency Non-Carrier
dihydrolipoamide dehydrogenase deficiency Non-Carrier
dihydropyrimidine dehydrogenase deficiency Non-Carrier
ethylmalonic encephalopathy Non-Carrier
familial dysautonomia Non-Carrier
familial hyperinsulinism, ABCC8-related Non-Carrier
familial mediterranean fever Non-Carrier
Fanconi anemia group C Non-Carrier
galactosemia, GALT-related Non-Carrier
Gaucher disease Non-Carrier
glutaric acidemia type 1 Non-Carrier
glutathione synthetase deficiency Non-Carrier
glycine encephalopathy, GLDC-related Non-Carrier
glycogen storage disease type 1a Non-Carrier
glycogen storage disease type 1b Carrier
glycogen storage disease type II Non-Carrier
glycogen storage disease type IIIa Non-Carrier
glycogen storage disease type IIIb Non-Carrier
GRACILE syndrome Non-Carrier
hereditary fructose intolerance Non-Carrier
HMG-CoA lyase deficiency Non-Carrier
holocarboxylase synthetase deficiency Non-Carrier
homocystinuria, CBS-related Non-Carrier
Hurler syndrome Non-Carrier
hyperoxaluria type 1 Non-Carrier
hyperoxaluria type 2 Non-Carrier
Joubert syndrome 2 Non-Carrier
junctional epidermolysis bullosa, LAMA3-related Non-Carrier
junctional epidermolysis bullosa, LAMB3-related Non-Carrier
junctional epidermolysis bullosa, LAMC2-related Non-Carrier
Krabbe disease Non-Carrier
LCHAD deficiency Non-Carrier
Leigh syndrome, French-Canadian type Non-Carrier
maple syrup urine disease type 1a Non-Carrier
maple syrup urine disease type 1b Non-Carrier
MCAD deficiency Non-Carrier
metachromatic leukodystrophy Non-Carrier
methylmalonic acidemia, MMAA-related Non-Carrier
methylmalonic acidemia, MMAB-related Non-Carrier
methylmalonic acidemia, MUT-related Non-Carrier
methylmalonic aciduria and homocystinuria type cblC Non-Carrier
mucolipidosis type IV Non-Carrier
mucopolysaccharidosis type 1 Non-Carrier
nemaline myopathy, NEB-related Non-Carrier
nephrotic syndrome, NPHS1-related Non-Carrier
nephrotic syndrome, NPHS2-related Non-Carrier
neuronal ceroid-lipofuscinosis, CLN3-related Non-Carrier
neuronal ceroid-lipofuscinosis, CLN5-related Non-Carrier
neuronal ceroid-lipofuscinosis, CLN8-related Non-Carrier
neuronal ceroid-lipofuscinosis, PPT1-related Non-Carrier
neuronal ceroid-lipofuscinosis, TPP1-related Non-Carrier
Niemann-Pick disease type A Non-Carrier
Niemann-Pick disease type B Non-Carrier
Niemann-Pick disease type C, NPC1-related Non-Carrier
Niemann-Pick disease type C, NPC2-related Non-Carrier
Nijmegen breakage syndrome Non-Carrier
non-ketotic hyperglycinemia, GLDC-related Non-Carrier
phenylalanine hydroxylase deficiency Non-Carrier
polycystic kidney disease, autosomal recessive Non-Carrier
Pompe disease Non-Carrier
primary hyperoxaluria type 1 Non-Carrier
primary hyperoxaluria type 2 Non-Carrier
propionic acidemia, PCCA-related Non-Carrier
propionic acidemia, PCCB-related Non-Carrier
rhizomelic chondrodysplasia punctata type 1 Non-Carrier
Salla disease Non-Carrier
Sandhoff disease Non-Carrier
sickle cell disease Non-Carrier
Sjogren-Larsson syndrome Non-Carrier
Smith-Lemli-Opitz syndrome Non-Carrier
sulfate transporter-related osteochondrodysplasias Non-Carrier
Tay-Sachs disease Non-Carrier
tyrosinemia type 1 Non-Carrier
Usher syndrome type 1F Non-Carrier
Usher syndrome type III Non-Carrier
Walker-Warburg syndrome, FKTN-related Non-Carrier
Wilson disease Non-Carrier
Zellweger syndrome spectrum, PEX-1 related, includes infantile refsum disease, neonatal adrenoleukodystrophy, and Zellweger syndrome (PEX1) Non-Carrier
spinal muscular atrophy  No disease-causing mutations detected (2 copies or more)