Meet Socrates (10030) – Open ID Donor.

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Socrates is a handsome young man with thick, wavy brown hair and matching brown eyes. He has angular facial features and a wide smile with straight white teeth (which was accomplished without the use of braces). Socrates has a medium skin tone with a few freckles across his cheeks and bridge of his nose. He is usually clean shaven and has a muscular build from regular cardio and weight lifting. Socrates is a very handsome, clean-cut donor.


Aside from his good looks, Socrates is also very intelligent. He is currently in medical school and hopes to work not only as a doctor, but also run a business that teaches healthy lifestyle habits. He is incredibly health conscious and is always willing to offer any advice to those who need it. Although he does not have much time for activities outside of school, Socrates was both musical and athletic in his younger days. He is also extremely well-traveled and we believe that all his life experiences have shaped Socrates into an amazing young man and wonderful donor.

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.

Karyotyping  Normal Male Karyoptype, 46XY
ABCC8-related hyperinsulinism Non-Carrier
alpha thalassemia Non-Carrier
ARSACS Non-Carrier
Bloom syndrome Non-Carrier
Canavan disease Non-Carrier
cystic fibrosis Non-Carrier
familial dysautonomia Non-Carrier
Fanconi anemia type C Non-Carrier
Gaucher disease Non-Carrier
glycogen storage disease type Ia Non-Carrier
Hb beta chain-related hemoglobinopathy (including beta thalassemia and sickle cell disease) No disease-causing mutations detected; normal complete blood count and hemoglobin analysis
hexosaminidase A deficiency (including Tay-Sachs disease) Non-Carrier
Joubert syndrome 2 Non-Carrier
lipoamide dehydrogenase deficiency Non-Carrier
maple syrup urine disease type 1B Non-Carrier
mucolipidosis IV Non-Carrier
NEB-related nemaline myopathy Non-Carrier
Niemann-Pick disease, SMPD1-associated Non-Carrier
spinal muscular atrophy No disease-causing mutations detected (2 copies or more)
Usher syndrome type 1F Non-Carrier
Usher syndrome type 3 Non-Carrier
Walker-Warburg syndrome Non-Carrier