To view current Seattle Sperm Bank Donor Availabilities please visit the following link of SSB Donors on CanAm Cryoservices website
Meet Declan (12217) – Open ID Donor – New Donor!
Trouvez un Donneur
- Yeux : Bleu
- Cheveux : Noirs
- Taille : 5'10"
- Poids (en livres) : 160
- Groupe sanguin : O Rh+
- CMV : -
- Origine ethnique : Mix, Filipino, German, Swedish
- Ascendance juive : Non
- Éducation/profession : B.S. Biology / Biologist
- Grossesse confirmée : Oui
- Informed Consent Form
Résultats des tests génétiques
- Dépistage étendu : Counsyl Universal Panel moins les maladies liées au X (au moins 102 maladies)
- Transporteur pour :
- Résultats pour Karyotyping / Amyotrophie musculaire spinale :
- Amyotrophie musculaire spinale: No disease causing mutations detectedative
- Résultats sans maladie causant des mutations : Découvre
- Karyotyping
- Cystic Fibrosis
- ABCC8-related Hyperinsulinism
- 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
- 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
- Homocystinuria Caused By Cystathionine Beta-synthase Deficiency
- Inclusion Body Myopathy 2
- Isovaleric Acidemia
- Joubert Syndrome 2
- Junctional Epidermolysis Bullosa, LAMA3-related
- Krabbe Disease
- 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
- Sandhoff Disease
- Segawa Syndrome
- Short Chain Acyl-CoA Dehydrogenase Deficiency
- Sjogren-Larsson Syndrome
- Smith-Lemli-Opitz Syndrome
- 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
- Nephrotic Syndrome (NPHS2-Related)
Description du Donneur
Declan is both smart and handsome. His diverse heritage has given him a very striking and unique look with thick, dark hair; light olive skin; and light blue, almond-shaped eyes.
Declan is a personable, kind, and altruistic man who puts a lot of focus on his career in healthcare, cultural awareness, and humanitarian work. He currently works in tissue donation and plans on completing medical school to begin work as a physician. Much of his time is devoted to international humanitarian healthcare initiatives. We think he is an amazing guy and we are thrilled to be able to offer him as a donor.
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Informations détaillées
| Interview audio | $0.00 |  |
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| Profil étendu | $0.00 | |
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| Keirsey Test | $0.00 | |
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| Genetic Test Results | Non disponible | ||
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