To view current Seattle Sperm Bank Donor Availabilities please visit the following link of SSB Donors on CanAm Cryoservices website
Meet Henry (10069) – Open ID Donor
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- Eyes: Blue
- Hair: Blonde
- Height: 6'01"
- Weight (lbs): 185
- Blood: B Rh-
- CMV: -
- Ethnicity: Caucasian, English, German, Scots-Irish, Scottish
- Jewish Ancestry: No
- Education/Occupation: B.A. History, M.S. International Relations / Study Abroad Advisor
- Live Birth / Pregnancy Confirmed: No
- Informed Consent Form
Test Results
- Extended Testing: Counsyl Fundamental Panel Plus (at least 21 conditions)
- Carrier For:
- NEB-related Nemaline Myopathy: Carrier
- Pseudocholinesterase Deficiency: Carrier
- Nephrotic Syndrome (NPHS2-Related): Carrier
- Results for Karyotyping / Spinal Muscular Atrophy:
- Spinal Muscular Atrophy: Copy number 2
- Results with No Disease Causing Mutations: View full list
- 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
- Autosomal Recessive Polycystic Kidney Disease
- 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
- Choroideremia
- 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
- 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
- Hereditary Thymine-uraciluria
- 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
- Hurler Syndrome
- Hypophosphatasia, Autosomal Recessive
- Inclusion Body Myopathy 2
- Isovaleric Acidemia
- Joubert Syndrome 2
- Junctional Epidermolysis Bullosa, LAMA3-related
- Krabbe Disease
- Limb-girdle Muscular Dystrophy Type 2D
- Limb-girdle Muscular Dystrophy Type 2E
- 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
- Muscle-eye-brain Disease
- 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
- Pycnodysostosis
- Rhizomelic Chondrodysplasia Punctata Type 1
- Salla 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 1F
- Usher Syndrome Type 3
- Very Long Chain Acyl-CoA Dehydrogenase Deficiency
- Walker-Warburg Syndrome
- Wilson Disease
- X-linked Juvenile Retinoschisis
Donor Description
Henry stands just over six feet tall with a very clean cut look. He has short blond hair and bright blue eyes. He keeps his hair short and his face clean shaven, showing off a strong jawline. Henry has a naturally athletic physique with lean muscles from regular exercise and previous sports training. He has a fair complexion with a few freckles here and there. He has straight white teeth and a wide smile with full pink lips.
Henry is open-minded and adventurous. Ever since his first venture out of the country, Henry has had a desire to travel the world and has turned this passion into a career. He took his graduate studies as a chance to pursue his passion and now works mentoring and advising college students on study abroad opportunities. Henry is well suited for this position as he is adaptable, creative and friendly with a laid-back demeanor and a genuine interest in seeing others succeed.
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Extended Info
| Audio Interview | $0.00 |  |
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| Baby Photo | $0.00 | |
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| Extended Profile | $0.00 | |
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| Keirsey Test | $0.00 | |
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| Staff Impression |
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| Genetic Test Results | Coming Soon | ||
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