Meet Aristotle (10027) – Open ID Donor.

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  • Eyes: Blue
  • Hair: Blonde
  • Height: 6'00"
  • Weight (lbs): 220
  • Blood: A Rh+
  • CMV: -
  • Ethnicity: Mix, Dutch, French-Canadian, German, Irish, Mexican
  • Jewish Ancestry: Yes
  • Education/Occupation: M.A. Forensic Anthropolgy and Religious Studies, B.A. Anthropology / Archaeological Monitor
  • Live Birth / Pregnancy Confirmed: Yes
  • Extended Testing: Yes
  • Genetically tested for: View


Open Donor: Aristotle

Staff Impression


Aristotle stands at six foot even with broad shoulders. He exercises regularly by doing martial arts and cardiovascular activities. Aristotle has thick, wavy blonde hair and with a fair skin tone. He also has a thick beard that he keeps neatly trimmed so it does not hide his wide smile or dimples. Aristotle’s most noticeable trait is probably his piercing blue eyes that light up when he talks about something he is passionate about.

Aristotle has a very calm, laid back demeanor but is passionate when it comes to issues he believes in. He is hard diligent and thorough with a wide variety of interests ranging from music to wildlife conservation to anthropology and his own heritage. Aristotle is incredibly hardworking and always looking to learn new things and increase his own knowledge. He is also caring and compassionate, always looking to develop more than superficial relationships with those around him. We believe that it his easy going personality coupled with his compassion and hardworking personality make Aristotle a 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