To view current Seattle Sperm Bank Donor Availabilities please visit the following link of SSB Donors on CanAm Cryoservices website
Meet Desmond (9644) – Open ID Donor
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- Eyes: Blue
- Hair: Brown
- Height: 5'11"
- Weight (lbs): 170
- Blood: A Rh+
- CMV: -
- Ethnicity: Caucasian, Dutch, English, French, French-Canadian, German
- Jewish Ancestry: No
- Education/Occupation: B.A. Music and Music Education
- Live Birth / Pregnancy Confirmed: No
Test Results
- Extended Testing: No
- Carrier For:
- No disease causing mutations detected
- Results for Karyotyping / Spinal Muscular Atrophy:
- Spinal Muscular Atrophy: Copy number 2
- Results with No Disease Causing Mutations: View full list
- 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
- Bardet-Biedl Syndrome, BBS10-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 Ib
- 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)
Donor Description
Desmond has a very youthful appearance. He has thick dark brown hair streaked with light brown highlights that he wears long. He has kind eyes and a soft, sweet smile. He has a flawless pale complexion with two small dimples gracing his cheeks. Desmond dresses fashionably in a mix of bohemian and hipster style with a focus on comfort and dark coloration.
Desmond is musically gifted and incredibly talented. He is pursuing music and hopes to write film scores in the future. Desmond is quiet and reserved but very kind and genuine. He is truly a gentle soul and wonderfully sweet individual. We asked Desmond what he was most proud of and he said, “I am definitely most proud of my musical skills, most notable, my piano playing abilities and music writing abilities. I am most proud of this because it is what I get complimented on most, and it is what I put most of my energy towards in life.” We think Desmond would make a fantastic genetic contribution to your family.
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Extended Info
| Audio Interview | Coming Soon | ||
| Baby Photo | $0.00 |  |
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| Extended Profile | Coming Soon | ||
| Keirsey Test | Coming Soon | ||
| Staff Impression | Coming Soon | ||
| Genetic Test Results | Coming Soon | ||
English 
French