Meet Roscoe (8755) – Open ID Donor.

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Roscoe is highly intelligent, thoughtful, and philanthropic in nature.  When we asked what his ultimate ambition in life is he responded, “To treat everyone with dignity and respect and to give back more than what I take. To always sleep soundly knowing that I did the very best that I could.”

Roscoe has light blue eyes and medium-dark brown hair.  He has a light skin complexion and very symmetrical features.  He dresses in a casual and trendy fashion.  He is athletically inclined and has a naturally lean physique.

Roscoe has many interests but his two main loves are film making and music.  He has released albums and written many pieces of music and currently works producing a well known documentary television show amongst his own film making projects.  He is multifaceted and an individual worth getting to know better, he is what we hope all donors to be like in so many aspects, Roscoe is a wonderful donor choice.

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
achromatopsia Non-Carrier
alkaptonuria Non-Carrier
alpha-1 antitrypsin deficiency Non-Carrier
alpha-mannosidosis Non-Carrier
alpha thalassemia Non-Carrier
Andermann syndrome Non-Carrier
ARSACS Non-Carrier
aspartylglycosaminuria Non-Carrier
ataxia with vitamin E deficiency Non-Carrier
ataxia-telangiectasia Non-Carrier
autosomal recessive polycystic kidney disease Non-Carrier
Bardet-Biedl syndrome, BBS1-related Non-Carrier
Bardet-Biedl syndrome, BBS10-related Non-Carrier
Biotinidase Deficiency Non-Carrier
Bloom syndrome Non-Carrier
Canavan disease Non-Carrier
carnitine palmitoyltransferase 1A deficiency Non-Carrier
carnitine palmitoyltransferase II deficiency Non-Carrier
cartilage-hair hypoplasia Non-Carrier
choroideremia Non-Carrier
citrullinemia type 1 Non-Carrier
CLN3-related neuronal ceroid lipofuscinosis Non-Carrier
CLN5-related neuronal ceroid lipofuscinosis Non-Carrier
Cohen syndrome Non-Carrier
21-hydroxylase deficient congenital adrenal hyperplasia Non-Carrier
congenital disorder of glycosylation type 1a Non-Carrier
congenital disorder of glycosylation type 1b Non-Carrier
congenital Finnish nephrosis Non-Carrier
Costeff optic atrophy syndrome Non-Carrier
cystic fibrosis Non-Carrier
cystinosis Non-Carrier
D-bifunctional protein deficiency Non-Carrier
factor V Leiden thrombophilia Non-Carrier
factor XI deficiency Non-Carrier
familial dysautonomia Non-Carrier
familial Mediterranean fever Non-Carrier
Fanconi anemia type C Non-Carrier
fragile X syndrome Non-Carrier
galactosemia Non-Carrier
Gaucher disease Non-Carrier
GJB2-related DFNB1 nonsyndromic hearing loss and deafness Non-Carrier
glucose-6-phosphate dehydrogenase deficiency Non-Carrier
glutaric acidemia type 1 Non-Carrier
glycogen storage disease type Ia Non-Carrier
glycogen storage disease type Ib Non-Carrier
glycogen storage disease type III Non-Carrier
glycogen storage disease type V Non-Carrier
GRACILE syndrome 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
hereditary fructose intolerance Non-Carrier
hereditary thymine-uraciluria Non-Carrier
Herlitz junctional epidermolysis bullosa, LAMA3-related Non-Carrier
Herlitz junctional epidermolysis bullosa, LAMB3-related Non-Carrier
Herlitz junctional epidermolysis bullosa, LAMC2-related Non-Carrier
hexosaminidase A deficiency (including Tay-Sachs disease) Non-Carrier
HFE-Associated Hereditary Hemochromatosis Non-Carrier
homocystinuria caused by cystathionine beta-synthase deficiency Non-Carrier
Hurler syndrome Non-Carrier
hypophosphatasia, autosomal recessive Non-Carrier
inclusion body myopathy 2 Non-Carrier
isovaleric acidemia Non-Carrier
Joubert syndrome 2 Non-Carrier
Krabbe disease Non-Carrier
limb-girdle muscular dystrophy type 2D Non-Carrier
limb-girdle muscular dystrophy type 2E Non-Carrier
lipoamide dehydrogenase deficiency Non-Carrier
long chain 3-hydroxyacyl-CoA dehydrogenase deficiency Non-Carrier
maple syrup urine disease type 1B Non-Carrier
medium chain acyl-CoA dehydrogenase deficiency Non-Carrier
megalencephalic leukoencephalopathy with subcortical cysts Non-Carrier
metachromatic leukodystrophy Non-Carrier
MTHFR deficiency Non-Carrier
mucolipidosis IV Non-Carrier
muscle-eye-brain disease Non-Carrier
NEB-related nemaline myopathy Non-Carrier
Niemann-Pick disease type C Non-Carrier
Niemann-Pick disease, SMPD1-associated Non-Carrier
Nijmegen breakage syndrome Non-Carrier
Northern epilepsy Non-Carrier
Pendred syndrome Non-Carrier
PEX1-related Zellweger Syndrome Spectrum Non-Carrier
phenylalanine hydroxylase deficiency Non-Carrier
polyglandular autoimmune syndrome type 1 Non-Carrier
Pompe disease Non-Carrier
PPT1-related neuronal ceroid lipofuscinosis Non-Carrier
primary carnitine deficiency Non-Carrier
primary hyperoxaluria type 1 Non-Carrier
primary hyperoxaluria type 2 Non-Carrier
PROP1-related combined pituitary hormone deficiency Non-Carrier
prothrombin thrombophilia Non-Carrier
pseudocholinesterase deficiency Non-Carrier
pycnodysostosis Non-Carrier
rhizomelic chondrodysplasia punctata type 1 Non-Carrier
Salla disease Non-Carrier
Segawa syndrome Non-Carrier
short chain acyl-CoA dehydrogenase deficiency Non-Carrier
Sjogren-Larsson syndrome Non-Carrier
Smith-Lemli-Opitz syndrome Non-Carrier
spinal muscular atrophy No disease-causing mutations detected (2 copies or more)
steroid-resistant nephrotic syndrome Non-Carrier
sulfate transporter-related osteochondrodysplasia Non-Carrier
TPP1-related neuronal ceroid lipofuscinosis Non-Carrier
tyrosinemia type 1 Non-Carrier
Usher syndrome type 1F Non-Carrier
Usher syndrome type 3 Non-Carrier
very long chain acyl-CoA dehydrogenase deficiency Non-Carrier
Walker-Warburg syndrome Non-Carrier
Wilson disease Non-Carrier
x-linked juvenile retinoschisis Non-Carrier