Meet Orson (12073) – Open ID Donor.

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Orson’s face is smart, caring, and bright. He has an oval face, a dazzling smile, and cute dimples. His sandy, light brown hair and bright blue eyes, coupled with his fair skin and subtle rosy undertones, give him a beachy vibe that is universally attractive. Orson is a prolific wrestler, and has the physique to show for it- solid medium frame, slender torso, and strong legs, arms, and shoulders.

If there were an award for “Nicest Person on the Planet,” Orson would certainly be a contender. He is altruistic to a fault, kind, generous, and seems to always puts everyone’s wellbeing above his own. He stays incredibly busy, with his day job as an Engineer and his side jobs as a volunteer and member of the board of multiple non-profit organizations. He has an intimate relationship with his parents and siblings and praises their close relationships. Orson is all around a compassionate, smart, motivated, and inspiring young man, and we are so happy to have him in our donor program!

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