Meet BFA0102 (BFA0102)
New Donor
BFA0102 is our very own Daniel Radcliffe lookalike. He is 177cm tall with blue-green eyes,
straight dark brown hair, and fair skin that tans easily. He leads a very active lifestyle and
particularly enjoys running. He is easy-going, reflective, optimistic, and practical, with a love of
maths and science.
He works in information technology—a field he cares deeply about, as it allows him to help protect
systems and solve complex problems. He is talented across a wide range of areas: technical,
practical, athletic, and even artistic, making him a true all-rounder.
He is gentle, polite, and caring. He always takes the time to ask how we are and enjoys sharing
stories. Though he may take a moment or two to warm up, once comfortable he is genuinely
engaging, interesting, and a pleasure to talk to.
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Meet BFA0102 (BFA0102)
New Donor
BFA0102 is our very own Daniel Radcliffe lookalike. He is 177cm tall with blue-green eyes,
straight dark brown hair, and fair skin that tans easily. He leads a very active lifestyle and
particularly enjoys running. He is easy-going, reflective, optimistic, and practical, with a love of
maths and science.
He works in information technology—a field he cares deeply about, as it allows him to help protect
systems and solve complex problems. He is talented across a wide range of areas: technical,
practical, athletic, and even artistic, making him a true all-rounder.
He is gentle, polite, and caring. He always takes the time to ask how we are and enjoys sharing
stories. Though he may take a moment or two to warm up, once comfortable he is genuinely
engaging, interesting, and a pleasure to talk to.
Blue/Green
Dark Brown
177
72
O Rh+
+
British, Indian
No
BSC in Computer Science / Game Developer
Yes
Routine Genetic Testing (at least 3 conditons)
-
- Spinal Muscular Atrophy : No disease causing mutations detectedative
-
- Cystic Fibrosis
- Adenosine Deaminase Deficiency
- ABCC8-related Hyperinsulinism
- Alkaptonuria
- Alpha-mannosidosis
- Alpha Thalassemia
- Andermann Syndrome
- Argininosuccinic Aciduria
- 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
- Citrullinemia Type 1
- CLN5-related Neuronal Ceroid Lipofuscinosis
- CLN8-related Neuronal Ceroid Lipofuscinosis
- Cohen Syndrome
- 21-hydroxylase Deficient Congenital Adrenal Hyperplasia
- Congenital Disorder Of Glycosylation Type Ia
- Congenital Disorder Of Glycosylation Type Ib
- Costeff Optic Atrophy Syndrome
- Cystinosis
- D-bifunctional Protein Deficiency
- Dihydrolipoamide Dehydrogenase Deficiency
- Ethylmalonic Encephalopathy
- 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
- HMG-CoA Lyase Deficiency
- Holocarboxylase Synthetase Deficiency
- 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
- Junctional Epidermolysis Bullosa, LAMB3-related
- Junctional Epidermolysis Bullosa, LAMC2-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 1A
- Maple Syrup Urine Disease Type 1B
- Medium Chain Acyl-CoA Dehydrogenase Deficiency
- Megalencephalic Leukoencephalopathy With Subcortical Cysts
- 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
- Muscle-eye-brain Disease
- NEB-related Nemaline Myopathy
- Niemann-Pick Disease, SMPD1-associated
- Nijmegen Breakage Syndrome
- 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
- Propionic Acidemia, PCCB-Related
- PROP1-related Combined Pituitary Hormone Deficiency
- Pseudocholinesterase Deficiency
- Pycnodysostosis
- Rhizomelic Chondrodysplasia Punctata Type 1
- Salla Disease
- Sandhoff 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 1F
- Usher Syndrome Type 3
- Very Long Chain Acyl-CoA Dehydrogenase Deficiency
- Walker-Warburg Syndrome
- Wilson Disease
- Maple Syrup Urine Disease Type II
- 6-pyruvoyl-tetrahydropterin Synthase Deficiency
- 11-beta-hydroxylase-deficient Congenital Adrenal Hyperplasia
- AMT-related Glycine Encephalopathy
- Argininemia
- Autosomal Recessive Osteopetrosis Type 1
- Bardet-Biedl Syndrome, BBS12-related
- Bardet-Biedl Syndrome, BBS2-related
- Calpainopathy
- Cerebrotendinous Xanthomatosis
- CLN6-related Neuronal Ceroid Lipofuscinosis
- COL4A3-related Alport Syndrome
- COL4A4-related Alport Syndrome
- Congenital Disorder Of Glycosylation Type Ic
- Delta-sarcoglycanopathy
- Dysferlinopathy
- ERCC6-related Disorders
- ERCC8-related Disorders
- EVC-related Ellis-van Creveld Syndrome
- EVC2-related Ellis-van Creveld Syndrome
- Fanconi Anemia Complementation Group A
- FKRP-related Disorders
- Galactokinase Deficiency
- Gamma-sarcoglycanopathy
- GLB1-related Disorders
- GLDC-related Glycine Encephalopathy
- GNPTAB-related Disorders
- KCNJ11-related Familial Hyperinsulinism
- Leigh Syndrome, French-Canadian Type
- Lipoid Congenital Adrenal Hyperplasia
- Lysosomal Acid Lipase Deficiency
- MKS1-related Disorders
- Mucopolysaccharidosis Type IIIA
- Mucopolysaccharidosis Type IIIB
- Mucopolysaccharidosis Type IIIC
- MYO7A-related Disorders
- Niemann-Pick Disease Type C2
- Peroxisome Biogenesis Disorder Type 4
- Peroxisome Biogenesis Disorder Type 5
- Peroxisome Biogenesis Disorder Type 6
- Primary Hyperoxaluria Type 3
- Pyruvate Carboxylase Deficiency
- RTEL1-related Disorders
- TGM1-related Autosomal Recessive Congenital Ichthyosis
- Tyrosinemia Type II
- USH1C-related Disorders
- USH2A-related Disorders
- Xeroderma Pigmentosum Group A
- Xeroderma Pigmentosum Group C
- 3-Beta-Hydroxysteroid Dehydrogenase Type II Deficiency
- 3-Methylcrotonyl-CoA Carboxylase Deficiency (MCCC1-Related)
- 3-Methylcrotonyl-CoA Carboxylase Deficiency (MCCC2-Related)
- 3-Phosphoglycerate Dehydrogenase Deficiency (PHGDH)
- Abetalipoproteinemia (MTTP)
- Acrodermatitis Enteropathica
- Acute Infantile Liver Failure
- Acyl-CoA Oxidase I Deficiency
- Anterior Segment Dysgenesis (CYP1B1-related) / Glaucoma (CYP1B1-relate
- Antley-Bixler Syndrome (POR-related)
- Aromatase Deficiency
- Arthrogryposis, Mental Retardation, And Seizures (SLC35A3)
- Asparagine Synthetase Deficiency
- Bardet-Biedl Syndrome (TRIM32-related)
- Bare Lymphocyte Syndrome, Type II
- Bartter Syndrome, Type 4A
- Beta-Ketothiolase Deficiency
- Carnitine Acylcarnitine Translocase Deficiency
- Carpenter Syndrome
- Cerebral Creatine Deficiency Syndrome 2
- Chediak-Higashi Syndrome
- Choreoacanthocytosis
- Chronic Granulomatous Disease (CYBA-related)
- Citrin Deficiency
- Congenital Adrenal Hyperplasia Due To 17-Alpha-Hydroxylase Deficiency
- Congenital Amegakaryocytic Thrombocytopenia (MPL)
- Congenital Ichthyosis 4A And 4B
- Congenital Insensitivity To Pain With Anhidrosis
- Congenital Myasthenic Syndrome (CHRNE-Related)
- Congenital Myasthenic Syndrome (DOK7-related)
- Congenital Myasthenic Syndrome (RAPSN-Related)
- Congenital Neutropenia (HAX1-Related)
- Congenital Secretory Chloride Diarrhea 1
- Corneal Dystrophy And Perceptive Deafness
- Corticosterone Methyloxidase Deficiency
- Cystinuria (SLC3A1-related)
- Deafness, Autosomal Recessive 3
- Deafness, Autosomal Recessive 77
- Dystrophic Epidermolysis Bullosa
- Ehlers-Danlos Syndrome, Type VIIC
- Enhanced S-Cone Syndrome
- Fanconi Anemia, Group G
- Gitelman Syndrome
- Glutaric Acidemia, Type IIa
- Glutaric Acidemia, Type IIb
- Glutaric Acidemia, Type IIc
- Glycogen Storage Disease, Type IV / Adult Polyglucosan Body Disease
- Glycogen Storage Disease, Type VII
- Hemochromatosis, Type 2A
- Hemochromatosis, Type 3
- Hereditary Leiomyomatosis And Renal Cell Cancer / Fumarase Deficiency
- Hereditary Spastic Paraparesis 49
- Hermansky-Pudlak Syndrome (HPS4-related)
- Hermansky-Pudlak Syndrome, Type 1
- Hermansky-Pudlak Syndrome, Type 3
- Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome
- Infantile Cerebral And Cerebellar Atrophy
- Leber Congenital Amaurosis (and Other GUCY2D-related Ciliopathies)
- Leber Congenital Amaurosis 10 And Other CEP290-Related Ciliopathies
- Leber Congenital Amaurosis 13
- Leber Congenital Amaurosis 2 / Retinitis Pigmentosa 20
- Leber Congenital Amaurosis 5
- Leukoencephalopathy With Vanishing White Matter
- Lipoprotein Lipase Deficiency
- Lysinuric Protein Intolerance
- Malonyl-CoA Decarboxylase Deficiency
- Microphthalmia / Anophthalmia
- Mitochondrial Complex I Deficiency (NDUFS6-Related)
- Mitochondrial DNA Depletion Syndrome 4A And 4B And Other POLG-related
- Mitochondrial DNA Depletion Syndrome 6 / Navajo Neurohepatopathy
- Mitochondrial Myopathy And Sideroblastic Anemia 1
- Mitochondrial Trifunctional Protein Deficiency (HADHB-Related)
- Mucopolysaccharidosis Type IIID
- Mucopolysaccharidosis Type IVa
- Mucopolysaccharidosis Type VI
- Mucopolysaccharidosis VII
- Multiple Pterygium Syndrome
- Multiple Sulfatase Deficiency (SUMF1)
- Myoneurogastrointestinal Encephalopathy
- Neuronal Ceroid-Lipofuscinosis (MFSD8-Related)
- Niemann-Pick Disease, Type C (NPC1-Related)
- Oculocutaneous Albinism (SLC45A2-related)
- Oculocutaneous Albinism (TYR-related)
- Oculocutaneous Albinism (TYRP1-related)
- Omenn Syndrome (RAG2-Related)
- Omenn Syndrome / Severe Combined Immunodeficiency, Athabaskan-Type
- Papillon-Lefevre Syndrome
- Pontocerebellar Hypoplasia, Type 1A
- Pontocerebellar Hypoplasia, Type 1B
- Pontocerebellar Hypoplasia, Type 2A And Type 4
- Pontocerebellar Hypoplasia, Type 2E
- Pontocerebellar Hypoplasia, Type 6
- Primary Ciliary Dyskinesia (DNAI1-Related)
- Primary Ciliary Dyskinesia (DNAI2-related)
- Progressive Cerebello-Cerebral Atrophy
- Progressive Familial Intrahepatic Cholestasis, Type 2
- Pyruvate Dehydrogenase E1-Beta Deficiency
- Renal Tubular Acidosis And Deafness
- Retinitis Pigmentosa 26
- Retinitis Pigmentosa 28
- Retinitis Pigmentosa 59 (DHDDS)
- Stuve-Wiedemann Syndrome
- Trichohepatoenteric Syndrome 1
- Usher Syndrome, Type ID
- Werner Syndrome
- Wolcott-Rallison Syndrome
- Nephrotic Syndrome (NPHS1-Related) / Congenital Finnish Nephrosis
- Nephrotic Syndrome (NPHS2-Related) / Steroid-Resistant Nephrotic Syndr
- ABCA4-related Conditions
- BRIP1-related Conditions (BRIP1)
- GDF5-related Conditions (GDF5)
- 17-beta Hydroxysteroid Dehydrogenase 3 Deficiency (HSD17B3)
- RLBP1-related Conditions (RLBP1)
- Steroid 5-alpha-reductase Deficiency (SRD5A2)
- Persistent Mullerian Duct Syndrome: Type I
- Persistent Mullerian Duct Syndrome: Type II
- Leydig Cell Hypoplasia (Luteinizing Hormone Resistance)
- Cystinuria: Non-type I
- Crigler-Najjar Syndrome