Meet Colton (12172)
Colton is a handsome, caring, thoughtful young man who is wise beyond his years. His deep-set brown eyes are kind and his smile charming. Colton is of average height and build. His thick dark hair suites his fair skin tone. He keeps a well-groomed full beard and prominent eyebrows.
Colton is a very talented writer, and artist. He spends his spare time either lost in a book, writing his screen play, or enjoying the beautiful Pacific Northwest on a walk with a four-legged friend. He has a very close relationship with his family and he thanks them for his positive outlook on caring for others. You can also find Colton volunteering his time to our local community. Colton is a perfect donor for our program and we think he could be the right donor for you.
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Meet Colton (12172)
Colton is a handsome, caring, thoughtful young man who is wise beyond his years. His deep-set brown eyes are kind and his smile charming. Colton is of average height and build. His thick dark hair suites his fair skin tone. He keeps a well-groomed full beard and prominent eyebrows.
Colton is a very talented writer, and artist. He spends his spare time either lost in a book, writing his screen play, or enjoying the beautiful Pacific Northwest on a walk with a four-legged friend. He has a very close relationship with his family and he thanks them for his positive outlook on caring for others. You can also find Colton volunteering his time to our local community. Colton is a perfect donor for our program and we think he could be the right donor for you.
Brown
Brown
175
70
B Rh+
-
Caucasian, English
Yes
B.A. English/Philosophy / Student, Editorial Assistant
Yes
Counsyl Universal Panel minus x-linked conditions (at least 102 conditions)
-
- No disease causing mutations detected
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- Spinal Muscular Atrophy : Copy Number 2
-
- 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
- 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
- Propionic Acidemia, PCCA-Related
- PROP1-related Combined Pituitary Hormone Deficiency
- Pseudocholinesterase 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
- TPP1-related Neuronal Ceroid Lipofuscinosis
- Tyrosinemia Type I
- Usher Syndrome Type 3
- Very Long Chain Acyl-CoA Dehydrogenase Deficiency
- Wilson Disease
- PCCA-related Propionic Acidemia
- Gitelman Syndrome
- Nephrotic Syndrome (NPHS2-Related) / Steroid-Resistant Nephrotic Syndr