|
171
|
|
|
FANCD2 and FANCI associated nuclease 1 |
KIAA1018, KMIN, MTMR15, hFAN1 |
Agnosia, Anxiety disorder, Attention deficit hyperactivity disorder, Benign neoplasm of nervous system, Carcinoma, Cardiac diverticulum, Colonic neoplasms, Colorectal neoplasms, Colorectal cancer, Developmental regression, Dysarthria, Dysgraphia, Dyskinetic syndrome, Glioblastoma, Hallucinations, Hemiplegia/hemiparesis, Hereditary nonpolyposis colorectal cancer, Huntington disease, Interstitial nephritis, Intestinal polyposis, Karyomegalic interstitial nephritis, Kidney disease, Liver carcinoma, Lynch syndrome, Malabsorption syndrome, Megalocytic interstitial nephritis, Mental depression, Migraine, Neoplasm of skeletal system, Nephritis, Nephronophthisis, Neuroblastoma, Ovarian neoplasm, Pancreatic adenocarcinoma, Pituitary adenoma, Rectal neoplasms, Thyroid neoplasm, Urologic neoplasmsView all (23 more) |
|
172
|
|
|
Forkhead box F1 |
ACDMPV, FKHL5, FREAC1 |
Alveolar capillary dysplasia, Annular pancreas, Anomalous pulmonary venous return, Aortic valve sclerosis, Atrial septal defect, Bicuspid aortic valve, Asplenia, Congenital atresia of pulmonary valve, Congenital diaphragmatic hernia, Posterolateral diaphragmatic hernia, Morgagni diaphragmatic hernia, Congenital malrotation of intestine, Duodenal atresia, Fetal megacystis, Agenesis of gallbladder, Gastrointestinal stromal tumor, Hirschsprung disease, Hydronephrosis, Hypertension, Hypertrophic pyloric stenosis, Hypoplastic left heart syndrome, Imperforate anus, Intestinal volvulus, Lung diseases, Mastocytosis, Meckel diverticulum, Patent ductus arteriosus, Persistent fetal circulation, Pulmonary arterial hypertension, Tetralogy of fallot, Urethral atresia, Vacterl association, Ventricular septal defectView all (18 more) |
|
173
|
|
|
Forkhead box F2 |
FKHL6, FREAC-2, FREAC2 |
|
|
174
|
|
|
Forkhead box C1 |
ARA, ASGD3, FKHL7, FREAC-3, FREAC3, IGDA, IHG1, IRID1, RIEG3 |
Aniridia, Anterior segment dysgenesis, Spinocerebellar ataxia, Atrial septal defect, Axenfeld anomaly, Cataract, Congenital anomaly of eye, Dandy-walker syndrome, Disorder of eye, Glaucoma, Glaucoma, congenital, Hearing loss, Hypodontia, Hypoplasia of iris, Hypoplasia of the maxilla, Hypospadias, Iridogoniodysgenesis, Iris hypoplasia with glaucoma, Microdontia, Nystagmus, Patent ductus arteriosus, Posterior embryotoxon, Proptosis, Prostatic neoplasms, Prostate cancer, Rieger syndrome, Open angle glaucoma, Strabismus, Stroke, Subcapsular cataract, Synechiae, Tetralogy of fallotView all (17 more) |
|
175
|
|
|
Forkhead box I1 |
FKH10, FKHL10, FREAC-6, FREAC6, HFH-3, HFH3 |
Compensated hypothyroidism, Congenital sensorineural hearing loss, Deafness, Hearing loss, Hyperparathyroidism, Hypothyroidism, Kidney disease, Leukemia, Mental retardation, Pendred syndrome, Renal tubular acidosis, Speech disorders, Thyroid carcinoma, Tracheal stenosis |
|
176
|
|
|
Forkhead box E3 |
AAT11, ASGD2, CATC3, CTRCT34, FKHL12, FREAC8 |
Aniridia, Anterior segment anomalies, Anterior segment dysgenesis, Aortic aneurysm, Aortic dissection, Aortic valve insufficiency, Arachnodactyly, Bicuspid aortic valve, Cataract, Coloboma of optic disc, Congenital aneurysm of ascending aorta, Congenital aphakia, Congenital exomphalos, Congenital ocular coloboma, Congenital primary aphakia, Corneal erosion, Corneal neovascularization, Coronary arteriosclerosis, Cutis marmorata, Descending aortic dissection, Developmental delay, Disorder of eye, Dyspnea, paroxysmal, Ectopia lentis, Glaucoma, Glaucoma, congenital, Hearing loss, Hypertension, Hypoplasia of the optic nerve, Ischemic stroke, Keratoconjunctivitis sicca, Keratoconus, Mental retardation, Microcornea, Microphthalmos, Nystagmus, Ocular hypertension, Patent ductus arteriosus, Peripheral arterial stenosis, Ptosis, Retinal dysplasia, Sclerocornea, Scoliosis, Segment dysgenesis, Strabismus, Subarachnoid hemorrhage, Subcapsular cataract, Synechiae, Thoracic aortic aneurysm and aortic dissection, Transient ischemic attackView all (35 more) |
|
177
|
|
|
F-box protein 21 |
FBX21 |
|
|
178
|
|
|
Fas apoptotic inhibitory molecule 2 |
LFG, LFG2, NGP35, NMP35, TMBIM2 |
|
|
179
|
|
|
Forkhead box J1 |
CILD43, FKHL13, HFH-4, HFH4 |
|
|
180
|
|
|
Forkhead box C2 |
FKHL14, LD, MFH-1, MFH1 |
Accessory kidney, Cardiovascular abnormalities, Cataract, Congenital diaphragmatic hernia, Posterolateral diaphragmatic hernia, Morgagni diaphragmatic hernia, Congenital musculoskeletal anomalies, Conjunctivitis, Corneal erosion, Corneal ulcer, Diabetes mellitus, Ectropion, Erosion of cornea, Fibrosarcoma, Hydrops fetalis, Lymphedema-distichiasis syndrome, Lymphedema-distichiasis syndrome with renal disease and diabetes mellitus, Neck webbing, Nephritis, Patent ductus arteriosus, Ptosis, Renal glomerular disease, Tetralogy of fallot, Ventricular septal defect, Vulval varicesView all (10 more) |
