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181
|
|
|
Forkhead box E1 |
BAMLAZ, FKHL15, FOXE2, HFKH4, HFKL5, NMTC4, TITF2, TTF-2, TTF2 |
Nonmedullary thyroid carcinoma, Bamforth-lazarus syndrome, Choanal atresia, Colonic neoplasms, Congenital hypothyroidism, Developmental delay, Dwarfism, Follicular thyroid carcinoma, Head and neck neoplasms, Hypersomnia, Hypothyroidism, Hypothyroidism, thyroidal, with spiky hair and cleft palate, Mental retardation, Lung diseases, Macroglossia, Nodular goiter, Papillary renal carcinoma, Papillary thyroid carcinoma, Spinal cord compression, Thyroid agenesis, Thyroid cancer, Thyroid carcinomaView all (7 more) |
|
182
|
|
|
Formin binding protein 1 |
FBP17 |
Ankylosing spondylitis, Arthritis, Autoimmune diseases, Autoimmune thyroiditis, Celiac disease, Common variable immunodeficiency, Crohn disease, Diabetes mellitus, Lupus erythematosus, Psoriasis, Ulcerative colitis |
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183
|
|
|
Forkhead box M1 |
FKHL16, FOXM1A, FOXM1B, FOXM1C, HFH-11, HFH11, HNF-3, INS-1, MPHOSPH2, MPP-2, MPP2, PIG29, TRIDENT |
|
|
184
|
|
|
Forkhead box O1 |
FKH1, FKHR, FOXO1A |
|
|
185
|
|
|
Forkhead box O3 |
AF6q21, FKHRL1, FKHRL1P2, FOXO2, FOXO3A |
|
|
186
|
|
|
Follistatin like 4 |
- |
|
|
187
|
|
|
Filaggrin |
ATOD2, FLG-1, FLG1 |
Asthma, Autism, Cerebellar hypoplasia, Cutis marmorata, Dermatitis, Developmental delay, Dysmorphic features, Eczema, Hypospadias, Ichthyosis, Ichthyosis vulgaris, Movement disorders, Myopia, Nystagmus, Osteopenia, Respiratory tract diseasesView all (1 more) |
|
188
|
|
|
Fli-1 proto-oncogene, ETS transcription factor |
BDPLT21, EWSR2, FLI-1, SIC-1 |
Agenesis of corpus callosum, Anemia, Annular pancreas, Anorexia, Aortic coarctation, Aortic valve sclerosis, Attention deficit hyperactivity disorder, Bipolar disorder, Bleeding disorder, Brain neoplasms, Cardiovascular abnormalities, Cataract, Cerebral atrophy, Clinodactyly, Congenital coloboma of iris, Congenital epicanthus, Congenital malrotation of intestine, Corneal astigmatism, Cryptorchidism, Developmental delay, Duodenal atresia, Dwarfism, Ectopic anus, Ectropion, Eczema, Endometrial neoplasms, Ewing sarcoma, Extra-osseous ewing`s sarcoma, Extraskeletal ewing sarcoma, Frontal bossing, Hydronephrosis, Hypoplastic left heart syndrome, Isolated delta-storage pool disease, Jacobsen syndrome, Macrocephaly, Major affective disorder, Medulloblastoma, Medullomyoblastoma, Mental retardation, Microcornea, Multicystic renal dysplasia, Myopia, Neck webbing, Neoplasm of scrotum, Ovarian neoplasm, Pachygyria, Pancreatic neoplasm, Pancreatitis, Paris-trousseau thrombocytopenia, Peripheral primitive neuroectodermal tumor, Precocious puberty, Proptosis, Ptosis, Schizophrenia, Scoliosis, Skeletal ewing sarcoma, Spina bifida, Spinal cord neoplasms, Strabismus, Syndactyly of fingers, Syndactyly of the toes, Talipes, Trigonocephaly, Ventricular septal defect, VitiligoView all (50 more) |
|
189
|
|
|
FLII actin remodeling protein |
CMD2J, FLI, FLIL, Fli1 |
Anxiety disorder, Attention deficit hyperactivity disorder, Brachycephaly, Brachydactyly, Camptodactyly of fingers, Developmental delay, Dwarfism, Dyssomnia, Frontal bossing, Gastroesophageal reflux disease, Hearing loss, Hypercholesterolemia, Hypothyroidism, Malocclusion, Mental retardation, Microcephaly, Microcornea, Micrognathism, Myopia, Obesity, Otitis media, Precocious puberty, Retinal detachment, Scoliosis, Sleep disorders, Smith-magenis syndrome, Speech disorders, Stereotyped behavior, Strabismus, Syndactyly of the toes, Synophrys, TaurodontismView all (17 more) |
|
190
|
|
|
FERM domain containing 4B |
6030440G05Rik, GRSP1 |
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