|
91
|
|
|
Fatty acid binding protein 3 |
FABP11, H-FABP, M-FABP, MDGI, O-FABP |
|
|
92
|
|
|
Fatty acid binding protein 5 |
E-FABP, EFABP, KFABP, PA-FABP, PAFABP |
|
|
93
|
|
|
Fatty acid binding protein 7 |
B-FABP, BLBP, FABPB, MRG |
|
|
94
|
|
|
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) |
|
95
|
|
|
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) |
|
96
|
|
|
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, High palate, Hirschsprung disease, Horseshoe kidney, Hydrocephalus, Hypertrophic cardiomyopathy, Hypogonadism, Hypoplasia of thumb, Hypospadias, Imperforate anus, Leukemia, Leukopenia, Liver carcinoma, 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) |
|
97
|
|
|
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) |
|
98
|
|
|
Fumarylacetoacetate hydrolase |
- |
Cholestasis, Cirrhosis, Fanconi syndrome, Glomerulonephritis, Glomerulosclerosis, Hypertrophic cardiomyopathy, Hypoglycemia, Hypophosphatemic rickets, Liver carcinoma, Liver failure, Nephrocalcinosis, Paralytic ileus, Periodic paralysis, Renal insufficiency, Tyrosinemia |
|
99
|
|
|
FA complementation group B |
FA2, FAAP90, FAAP95, FAB, FACB |
Anemia, Aqueductal stenosis, Arrhinencephaly, Astigmatism, Atrial septal defect, Azoospermia, Cafe-au-lait spot, Camptodactyly of fingers, Cataract, Choanal atresia, Anotia, Congenital arteriovenous malformation, Congenital epicanthus, Congenital exomphalos, Pulmonary hypoplasia, Congenital hypoplasia of radius, Cranial nerve paralysis, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Esophageal atresia, Fanconi anemia, Frontal bossing, Hernia, femoral, High palate, Hirschsprung disease, Hydrocephalus, Hydronephrosis, Hypertrophic cardiomyopathy, Hypogonadism, Hypospadias, Imperforate anus, Leukemia, Leukopenia, Head and neck cancer, Meckel diverticulum, Mental retardation, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Miller dieker syndrome, Monocytic leukemia, Myelodysplasia, Myelodysplastic syndrome, Nystagmus, Pancytopenia, Patent ductus arteriosus, Proptosis, Ptosis, Renal agenesis, Renal insufficiency, Sacral agenesis, Scoliosis, Spina bifida, Strabismus, Syndactyly of fingers, Syndactyly of the toes, Syndromic microphthalmia, Tetralogy of fallot, Thumb aplasia, Transposition of great vessels, Urethral atresia, Vacterl association, Vacterl association, x-linked, with or without hydrocephalus, Vater association with macrocephaly and ventriculomegalyView all (52 more) |
|
100
|
|
|
FA complementation group F |
FAF |
Astigmatism, Atrial septal defect, Azoospermia, Cafe-au-lait spot, Camptodactyly of fingers, Cataract, Choanal atresia, Congenital arteriovenous malformation, Congenital epicanthus, Congenital exomphalos, Cranial nerve paralysis, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Fanconi anemia, Frontal bossing, High palate, Hirschsprung disease, Hydrocephalus, Hypertrophic cardiomyopathy, Hypogonadism, Hypospadias, Imperforate anus, Leukemia, Leukopenia, Head and neck cancer, Meckel diverticulum, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Miller dieker syndrome, Monocytic leukemia, Myelodysplasia, Myelodysplastic syndrome, Nystagmus, Pancytopenia, Patent ductus arteriosus, Proptosis, Ptosis, Renal insufficiency, Scoliosis, Spina bifida, Strabismus, Syndactyly of fingers, Syndactyly of the toes, Tetralogy of fallotView all (33 more) |
