To view current Seattle Sperm Bank Donor Availabilities please visit the following link of SSB Donors on CanAm Cryoservices website
Meet Tristan (9607) – Open ID Donor
Trouvez un Donneur
- Yeux : Bleu
- Cheveux : Blonds
- Taille : 5'11"
- Poids (en livres) : 180
- Groupe sanguin : A Rh+
- CMV : +
- Origine ethnique : Caucasian, English, Hungarian
- Ascendance juive : Non
- Éducation/profession : A.A. Psychology / Personal Trainer and Model
- Grossesse confirmée : Oui
- Informed Consent Form
Résultats des tests génétiques
- Dépistage étendu : Non
- Transporteur pour :
- Bardet-Biedl Syndrome, BBS10-related: Porteur
- Glycogen Storage Disease Type Ib: Porteur
- Résultats pour Karyotyping / Amyotrophie musculaire spinale :
- Amyotrophie musculaire spinale: Copy number 2
- Résultats sans maladie causant des mutations : Découvre
- Karyotyping
- Cystic Fibrosis
- Adenosine Deaminase Deficiency
- ABCC8-related Hyperinsulinism
- Alpha-1 Antitrypsin Deficiency
- Andermann Syndrome
- Argininosuccinic Aciduria
- ARSACS
- Aspartylglycosaminuria
- Ataxia-telangiectasia
- Autosomal Recessive Polycystic Kidney Disease
- Bardet-Biedl Syndrome, BBS1-related
- Beta-Thalassemia
- Bloom Syndrome
- Canavan Disease
- Cartilage-hair Hypoplasia
- Citrullinemia Type 1
- CLN3-related Neuronal Ceroid Lipofuscinosis
- CLN5-related Neuronal Ceroid Lipofuscinosis
- CLN8-related Neuronal Ceroid Lipofuscinosis
- Cobalamin C Disease
- Congenital Disorder Of Glycosylation Type Ia
- Congenital Finnish Nephrosis
- Cystinosis
- D-bifunctional Protein Deficiency
- Dihydrolipoamide Dehydrogenase Deficiency
- Dihydropyrimidine Dehydrogenase Deficiency
- Ethylmalonic Encephalopathy
- Familial Dysautonomia
- Familial Mediterranean Fever
- Fanconi Anemia Type C
- Galactosemia
- Gaucher Disease
- Glutaric Acidemia Type 1
- Glutathione Synthetase Deficiency
- Glycine Encephalopathy
- Glycogen Storage Disease Type Ia
- Glycogen Storage Disease Type II
- Glycogen Storage Disease Type III
- GRACILE Syndrome
- Hb Beta Chain-related Hemoglobinopathy (including Beta Thalassemia And Sickle Cell Disease)
- Hereditary Fructose Intolerance
- HMG-CoA Lyase Deficiency
- Holocarboxylase Synthetase Deficiency
- Homocystinuria Caused By Cystathionine Beta-synthase Deficiency
- Hurler Syndrome
- Hyperoxaluria Type 1
- Hyperoxaluria Type 2
- Joubert Syndrome 2
- Junctional Epidermolysis Bullosa, LAMA3-related
- Junctional Epidermolysis Bullosa, LAMB3-related
- Junctional Epidermolysis Bullosa, LAMC2-related
- Krabbe Disease
- Long Chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency
- Leigh Syndrome
- Maple Syrup Urine Disease Type 1A
- Maple Syrup Urine Disease Type 1B
- Maple Syrup Urine Disease Type 3
- Medium Chain Acyl-CoA Dehydrogenase Deficiency
- Metachromatic Leukodystrophy
- Methylmalonic Acidemia MMAA-related
- Methylmalonic Acidemia MMAB-related
- Methylmalonic Acidemia MUT-related
- Methylmalonic Aciduria And Homocystinuria Type CbIC
- Mucolipidosis IV
- Mucopolysaccharidosis Type I
- NEB-related Nemaline Myopathy
- Niemann-Pick Disease Type A
- Niemann-Pick Disease Type B
- Niemann-Pick Disease Type C
- Nijmegen Breakage Syndrome
- Non-Ketonic Hyperglycinemia, GLDC-Related
- PEX1-related Zellweger Syndrome Spectrum
- Phenylalanine Hydroxylase Deficiency
- PPT1-related Neuronal Ceroid Lipofuscinosis
- Primary Hyperoxaluria Type 1
- Primary Hyperoxaluria Type 2
- Propionic Acidemia, PCCA-Related
- Propionic Acidemia, PCCB-Related
- Rhizomelic Chondrodysplasia Punctata Type 1
- Salla Disease
- Sandhoff Disease
- Sickle Cell Disease
- Sjogren-Larsson Syndrome
- Smith-Lemli-Opitz Syndrome
- Sulfate Transporter-related Osteochondrodysplasia (SLC26A2)
- Tay-Sachs Disease (Counsyl)
- TPP1-related Neuronal Ceroid Lipofuscinosis
- Tyrosinemia Type I
- Usher Syndrome Type 1F
- Usher Syndrome Type 3
- Walker-Warburg Syndrome
- Wilson Disease
- Nephrotic Syndrome (NPHS1-Related)
- Nephrotic Syndrome (NPHS2-Related)
Description du Donneur
Tristan is incredibly attractive and we can see why he works as a model. He has a chiseled jaw with a tiny cleft in the center of the chin. He has full red lips and a big smile. Tristan could easily rock the surfer look with his sandy blonde hair, big blue eyes, and naturally tanned skin. Tristan is very active and has the muscular physique to keep up with his many activities. He is typically seen in workout clothes or trendy sports clothes.
This donor is very intelligent and witty. He is currently enrolled in a top university to finish his psychology degree. Tristan loves to meet new people and is naturally gregarious. He is also charming and sweet. Tristan is a musician and plays the guitar and piano. He is very well rounded and we think he would make a fabulous genetic donor to your family.
Panier
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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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