Meet BFA0118 (BFA0118)
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Meet BFA0118 (BFA0118)
Brown
Light Brown
178
75
O Rh+
-
British
No
University Student / Business Student
No
No
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- No disease causing mutations detected
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- Cystic Fibrosis
- Adenosine Deaminase Deficiency
- ABCC8-related Hyperinsulinism
- Alpha-mannosidosis
- Alpha Thalassemia
- Andermann Syndrome
- Argininosuccinic Aciduria
- ARSACS
- Aspartylglycosaminuria
- Ataxia With Vitamin E Deficiency
- Biotinidase Deficiency
- Bloom Syndrome
- Canavan Disease
- Carnitine Palmitoyltransferase IA Deficiency
- Citrullinemia Type 1
- CLN3-related Neuronal Ceroid Lipofuscinosis
- CLN5-related Neuronal Ceroid Lipofuscinosis
- CLN8-related Neuronal Ceroid Lipofuscinosis
- Cobalamin C Disease
- Cohen Syndrome
- 21-hydroxylase Deficient Congenital Adrenal Hyperplasia
- Congenital Disorder Of Glycosylation Type Ia
- Costeff Optic Atrophy Syndrome
- Ethylmalonic Encephalopathy
- Familial Mediterranean Fever
- Galactosemia
- GJB2-related DFNB1 Nonsyndromic Hearing Loss And Deafness
- Glutathione Synthetase Deficiency
- Glycine Encephalopathy
- Glycogen Storage Disease Type Ia
- Hereditary Thymine-uraciluria
- 6-pyruvoyl-tetrahydropterin Synthase Deficiency
- 11-beta-hydroxylase-deficient Congenital Adrenal Hyperplasia
- Alstrom Syndrome
- AMT-related Glycine Encephalopathy
- Argininemia
- ATP7A-related Disorders
- Autosomal Recessive Osteopetrosis Type 1
- Calpainopathy
- CLN6-related Neuronal Ceroid Lipofuscinosis
- COL4A3-related Alport Syndrome
- ERCC6-related Disorders
- EVC2-related Ellis-van Creveld Syndrome
- Fanconi Anemia Complementation Group A
- FKRP-related Disorders
- GLB1-related Disorders
- Anterior Segment Dysgenesis (CYP1B1-related) / Glaucoma (CYP1B1-relate
- Asparagine Synthetase Deficiency
- Ataxia-Telangiectasia-Like Disorder (MRE11)
- Bilateral Frontoparietal Polymicrogyria
- Carnitine Acylcarnitine Translocase Deficiency
- Carpenter Syndrome
- Cerebral Dysgenesis, Neuropathy, Ichthyosis, And Palmoplantar Keratode
- Citrin Deficiency
- Congenital Bile Acid Synthesis Defect (HSD3B7-Related)
- Congenital Disorder Of Deglycosylation
- Corneal Dystrophy And Perceptive Deafness
- Corticosterone Methyloxidase Deficiency
- Cytochrome C Oxidase Deficiency / Leigh Syndrome (COX15-related)
- Diaphanospondylodysostosis
- Distal Renal Tubular Acidosis / Spherocytosis, Type 4
- Dystrophic Epidermolysis Bullosa
- Enhanced S-Cone Syndrome
- Familial Hypercholesterolemia (LDLR-related)
- Familial Hyperphosphatemic Tumoral Calcinosis
- Fanconi-Bickel Syndrome
- Fundus Albipunctatus (RDH5-related)
- Galactose Epimerase Deficiency
- Glanzmann Thrombasthenia (ITGA2B-related)
- Glutaric Acidemia, Type IIb
- Glutaric Acidemia, Type IIc
- Glycogen Storage Disease, Type IXb
- Glycogen Storage Disease, Type VI
- Gray Platelet Syndrome
- Growth Hormone Deficiency, Type IB
- Hawkinsinuria / Tyrosinemia, Type III
- Hereditary Leiomyomatosis And Renal Cell Cancer / Fumarase Deficiency
- Hereditary Spastic Paraparesis 49