To view current Seattle Sperm Bank Donor Availabilities please visit the following link of SSB Donors on CanAm Cryoservices website
Meet Redmond (12147) – Open ID Donor
Trouvez un Donneur
- Yeux : Bleu
- Cheveux : Bruns
- Taille : 5'09"
- Poids (en livres) : 170
- Groupe sanguin : A Rh+
- CMV : -
- Origine ethnique : Caucasian, German, Irish
- Ascendance juive : Non
- Éducation/profession : BA International Studies / Energy Efficiency Advisor
- Grossesse confirmée : Non
- Informed Consent Form
Résultats des tests génétiques
- Dépistage étendu : Counsyl Universal Panel moins les maladies liées au X (au moins 102 maladies)
- Transporteur pour :
- HFE-Associated Hereditary Hemochromatosis: Porteur
- Smith-Lemli-Opitz Syndrome: Porteur
- Résultats pour Karyotyping / Amyotrophie musculaire spinale :
- Amyotrophie musculaire spinale: Copy number 2
- Résultats sans maladie causant des mutations : Découvre
- Karyotyping
- Cystic Fibrosis
- ABCC8-related Hyperinsulinism
- Achromatopsia
- Alkaptonuria
- Alpha-1 Antitrypsin Deficiency
- Alpha-mannosidosis
- Alpha Thalassemia
- Andermann Syndrome
- ARSACS
- Aspartylglycosaminuria
- Ataxia With Vitamin E Deficiency
- Ataxia-telangiectasia
- Bardet-Biedl Syndrome, BBS1-related
- Bardet-Biedl Syndrome, BBS10-related
- Biotinidase Deficiency
- Bloom Syndrome
- Canavan Disease
- Carnitine Palmitoyltransferase IA Deficiency
- Carnitine Palmitoyltransferase II Deficiency
- Cartilage-hair Hypoplasia
- Citrullinemia Type 1
- CLN3-related Neuronal Ceroid Lipofuscinosis
- CLN5-related Neuronal Ceroid Lipofuscinosis
- Cohen Syndrome
- 21-hydroxylase Deficient Congenital Adrenal Hyperplasia
- Congenital Disorder Of Glycosylation Type Ia
- Congenital Disorder Of Glycosylation Type Ib
- Congenital Finnish Nephrosis
- Costeff Optic Atrophy Syndrome
- Cystinosis
- D-bifunctional Protein Deficiency
- Dihydropyrimidine Dehydrogenase Deficiency
- Factor XI Deficiency
- Familial Dysautonomia
- Familial Mediterranean Fever
- Fanconi Anemia Type C
- Galactosemia
- Gaucher Disease
- GJB2-related DFNB1 Nonsyndromic Hearing Loss And Deafness
- Glutaric Acidemia Type 1
- Glycogen Storage Disease Type Ia
- Glycogen Storage Disease Type Ib
- Glycogen Storage Disease Type II
- Glycogen Storage Disease Type III
- Glycogen Storage Disease Type V
- GRACILE Syndrome
- Hb Beta Chain-related Hemoglobinopathy (including Beta Thalassemia And Sickle Cell Disease)
- Hereditary Fructose Intolerance
- Herlitz Junctional Epidermolysis Bullosa, LAMB3-related
- Herlitz Junctional Epidermolysis Bullosa, LAMC2-related
- Hexosaminidase A Deficiency (including Tay-Sachs Disease)
- Homocystinuria Caused By Cystathionine Beta-synthase Deficiency
- Hypophosphatasia, Autosomal Recessive
- Inclusion Body Myopathy 2
- Isovaleric Acidemia
- Joubert Syndrome 2
- Junctional Epidermolysis Bullosa, LAMA3-related
- Krabbe Disease
- Long Chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency
- Maple Syrup Urine Disease Type 1B
- Medium Chain Acyl-CoA Dehydrogenase Deficiency
- Megalencephalic Leukoencephalopathy With Subcortical Cysts
- Metachromatic Leukodystrophy
- Mucolipidosis IV
- Mucopolysaccharidosis Type I
- Muscle-eye-brain Disease
- NEB-related Nemaline Myopathy
- Niemann-Pick Disease Type C
- Niemann-Pick Disease, SMPD1-associated
- Nijmegen Breakage Syndrome
- Northern Epilepsy
- Pendred Syndrome
- PEX1-related Zellweger Syndrome Spectrum
- Phenylalanine Hydroxylase Deficiency
- Polyglandular Autoimmune Syndrome Type 1
- PPT1-related Neuronal Ceroid Lipofuscinosis
- Primary Carnitine Deficiency
- Primary Hyperoxaluria Type 1
- Primary Hyperoxaluria Type 2
- PROP1-related Combined Pituitary Hormone Deficiency
- Pseudocholinesterase Deficiency
- Pycnodysostosis
- Rhizomelic Chondrodysplasia Punctata Type 1
- Salla Disease
- Segawa Syndrome
- Short Chain Acyl-CoA Dehydrogenase Deficiency
- Sulfate Transporter-related Osteochondrodysplasia (SLC26A2)
- TPP1-related Neuronal Ceroid Lipofuscinosis
- Tyrosinemia Type I
- Usher Syndrome Type 3
- Very Long Chain Acyl-CoA Dehydrogenase Deficiency
- Wilson Disease
- Congenital Amegakaryocytic Thrombocytopenia (MPL)
- Congenital Myasthenic Syndrome (CHRNE-Related)
Description du Donneur
Redmond has handsome, angular features, light brown hair, and striking blue eyes. He keeps a lean physique from staying active outdoors, running marathons, and playing multiple sports. He’s a natural athlete.
Redmond is a very driven, intelligent, and curious person who likes to stay aware of what is going on in the world. He is a charming and straightforward conversationalist, always ready to discuss politics and current events; his dry wit allows him to approach any topic with humor. Redmond has a genuine desire to help people build families of their own.
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Informations détaillées
| Interview audio | Non disponible | ||
| Photos | $0.00 |  |
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| Profil étendu | Non disponible | ||
| Keirsey Test | Non disponible | ||
| Impressions | Non disponible | ||
| Genetic Test Results | Non disponible | ||
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