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3081
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Aldehyde dehydrogenase 2 family member |
ALDH-E2, ALDHI, ALDM |
Asthma, Autoimmune diseases, Bipolar disorder, Colorectal cancer, Colorectal neoplasms, Coronary heart disease, Dermatitis, Esophagus neoplasm, Gout, Gouty arthritis, Industrial dermatosis, Ischemic stroke, Korsakoff psychosis, Melanosis, Melasma, Metabolic syndrome, Nasopharyngeal carcinoma, Necrotizing enterocolitis, Non-alcoholic fatty liver disease, Psoriasis, Stroke, Vascular diseasesView all (7 more) |
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3082
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Fatty acid binding protein 3 |
FABP11, H-FABP, M-FABP, MDGI, O-FABP |
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3083
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Fatty acid binding protein 5 |
E-FABP, EFABP, KFABP, PA-FABP, PAFABP |
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3084
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Fatty acid binding protein 7 |
B-FABP, BLBP, FABPB, MRG |
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3085
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FA complementation group A |
FA, FA-H, FA1, FAA, FACA, FAH, FANCH |
Adenocarcinoma, Anemia, Astigmatism, Atrial septal defect, Azoospermia, Urinary bladder cancer, Bladder neoplasm, Cafe-au-lait spot, Camptodactyly of fingers, Cataract, Choanal atresia, Compensatory hyperinsulinemia, Congenital arteriovenous malformation, Congenital epicanthus, Congenital exomphalos, Congenital heart defects, Cranial nerve paralysis, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Ectopic kidney, Endogenous hyperinsulinism, Estren-dameshek variant of fanconi pancytopenia, Exogenous hyperinsulinism, Fanconi anemia, Frontal bossing, High palate, Hirschsprung disease, Horseshoe kidney, Hydrocephalus, Hyperinsulinism, Hypertrophic cardiomyopathy, Hypogonadism, Hypoplasia of thumb, Hypospadias, Imperforate anus, Leukemia, Leukopenia, Head and neck cancer, Malignant melanoma of skin, Meckel diverticulum, Melanoma, Melanosis, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Miller dieker syndrome, Monocytic leukemia, Myelodysplasia, Myelodysplastic syndrome, Neutropenia, Nystagmus, Pancytopenia, Patent ductus arteriosus, Proptosis, Prostate adenocarcinoma, Ptosis, Renal agenesis, Renal insufficiency, Salivary gland neoplasm, Malignant neoplasm of salivary gland, Scoliosis, Spina bifida, Strabismus, Syndactyly of fingers, Syndactyly of the toes, Tetralogy of fallot, Thumb aplasia, VitiligoView all (56 more) |
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3086
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FA complementation group C |
FA3, FAC, FACC |
Anemia, Astigmatism, Atrial septal defect, Azoospermia, Benign neoplasm of bladder, Urinary bladder cancer, Bladder neoplasm, Bladder carcinoma, Cafe-au-lait spot, Camptodactyly of fingers, Hereditary cancer syndrome, Cataract, Choanal atresia, Colorectal cancer, Compensatory hyperinsulinemia, Congenital arteriovenous malformation, Congenital epicanthus, Congenital exomphalos, Congenital heart defects, Cranial nerve paralysis, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Ectopic kidney, Endogenous hyperinsulinism, Exogenous hyperinsulinism, Fanconi anemia, Frontal bossing, High palate, Hirschsprung disease, Horseshoe kidney, Hydrocephalus, Hyperinsulinism, Hypertrophic cardiomyopathy, Hypogonadism, Hypoplasia of thumb, Hypospadias, Imperforate anus, Leukemia, Leukopenia, Head and neck cancer, Meckel diverticulum, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Miller dieker syndrome, Monocytic leukemia, Myelodysplasia, Myelodysplastic syndrome, Neutropenia, Nystagmus, Pancytopenia, Patent ductus arteriosus, Proptosis, Ptosis, Renal agenesis, Renal insufficiency, Scoliosis, Spina bifida, Strabismus, Syndactyly of fingers, Syndactyly of the toes, Tetralogy of fallot, Thumb aplasia, Tracheoesophageal fistulaView all (52 more) |
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3087
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FA complementation group D2 |
FA-D2, FA4, FACD, FAD, FAD2, FANCD |
Anemia, Astigmatism, Atrial septal defect, Azoospermia, Cafe-au-lait spot, Camptodactyly of fingers, Cataract, Choanal atresia, Congenital arteriovenous malformation, Congenital epicanthus, Congenital exomphalos, Congenital heart defects, Cranial nerve paralysis, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Ectopic kidney, Fanconi anemia, Frontal bossing, Head and neck cancer, High palate, Hirschsprung disease, Horseshoe kidney, Hydrocephalus, Hypertrophic cardiomyopathy, Hypogonadism, Hypoplasia of thumb, Hypospadias, Imperforate anus, Leukemia, Leukopenia, Liver carcinoma, Meckel diverticulum, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Miller dieker syndrome, Monocytic leukemia, Myelodysplasia, Myelodysplastic syndrome, Neutropenia, Nystagmus, Pancytopenia, Patent ductus arteriosus, Proptosis, Ptosis, Renal agenesis, Renal insufficiency, Scoliosis, Spina bifida, Strabismus, Syndactyly of fingers, Syndactyly of the toes, Tetralogy of fallot, Thumb aplasiaView all (42 more) |
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3088
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FA complementation group E |
FACE, FAE |
Anemia, Astigmatism, Atrial septal defect, Azoospermia, Cafe-au-lait spot, Camptodactyly of fingers, Cataract, Choanal atresia, Colorectal cancer, Congenital arteriovenous malformation, Congenital epicanthus, Congenital exomphalos, Congenital heart defects, Cranial nerve paralysis, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Ectopic kidney, Fanconi anemia, Frontal bossing, High palate, Hirschsprung disease, Horseshoe kidney, Hydrocephalus, Hypertrophic cardiomyopathy, Hypogonadism, Hypoplasia of thumb, Hypospadias, Imperforate anus, Leukemia, Leukopenia, Head and neck cancer, Meckel diverticulum, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Miller dieker syndrome, Monocytic leukemia, Myelodysplasia, Myelodysplastic syndrome, Neutropenia, Nystagmus, Pancytopenia, Patent ductus arteriosus, Proptosis, Ptosis, Renal agenesis, Renal insufficiency, Scoliosis, Spina bifida, Strabismus, Syndactyly of fingers, Syndactyly of the toes, Tetralogy of fallot, Thumb aplasiaView all (42 more) |
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3089
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Aldehyde dehydrogenase 3 family member A1 |
ALDH3, ALDHIII |
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3090
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Acyl-CoA synthetase long chain family member 1 |
ACS1, FACL1, FACL2, LACS, LACS1, LACS2 |
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