Meet Amos (9899) – Open ID Donor.

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Amos has the quintessential boy-next-door look to him; he has thick brown hair, brown eyes, a pointed, defined nose, square jawline, and full lips. He has a medium, athletic build with a strong neck and shoulders. All around, he is very handsome!

Amos is a bit of a self-described strong, silent type, but definitely doesn’t come across as shy. He seems particularly introspective and well-spoken. His sense of curiosity and adventure has pushed him outside his comfort zone over the years to explore new places, and he is very open to new experiences. We love how fondly he speaks of his parents, and the moral values they instilled in him at a young age, as well as his passion and dedication to his schoolwork and future career goals. If you are looking for someone who is intuitive, hard-working, and open-minded, Amos would be a great choice for you.

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.

 

spinal muscular atrophyNo disease-causing mutations detected (2 copies or more)

Karyotyping  Normal Male Karyoptype, 46XY
Bloom syndrome Non-Carrier
Canavan disease Non-Carrier
cystic fibrosis Negative for 32 mutations
Dihydrolipoamide Dehydrogenase Non-Carrier
familial dysautonomia Non-Carrier
familial hyperinsulinism  Non-Carrier
Fanconi anemia type C Non-Carrier
Gaucher disease Non-Carrier
glycogen storage disease type Ia Non-Carrier
hexosaminidase A deficiency (including Tay-Sachs disease) Non-Carrier
Joubert syndrome 2 Non-Carrier
maple syrup urine disease Non-Carrier
mucolipidosis IV Non-Carrier
Nemaline Myopathy Non-Carrier
Niemann-Pick disease type A and B Non-Carrier
spinal muscular atrophy No disease-causing mutations detected (2 copies or more)
Usher syndrome type 1F Non-Carrier
Usher syndrome type III Non-Carrier
Walker-Warburg syndrome Non-Carrier