4801
|
|
|
Forkhead box A1 |
HNF3A, TCF3A |
|
4802
|
|
|
Forkhead box A2 |
HNF-3-beta, HNF3B, TCF3B |
|
4803
|
|
|
Forkhead box A3 |
FKHH3, HNF3G, TCF3G |
|
4804
|
|
|
Forkhead box B1 |
FKH5, HFKH-5 |
|
4805
|
|
|
Forkhead box B2 |
FKH4, bA159H20.4 |
|
4806
|
|
|
Forkhead box C1 |
ARA, ASGD3, FKHL7, FREAC-3, FREAC3, IGDA, IHG1, IRID1, RIEG3 |
Aniridia, Anterior segment dysgenesis, Anterior segment mesenchymal dysgenesis, Spinocerebellar ataxia, Axenfeld anomaly, Axenfeld-rieger syndrome, Congenital anomalies of the kidney and urinary tract, Cardiovascular disease, Coronary artery disease, Dandy-walker syndrome, Hypertension, Glaucoma, Iridogoniodysgenesis, Myocardial infarction, Prostatic neoplasms, Rieger syndrome, Tetralogy of fallotView all (2 more) |
4807
|
|
|
Forkhead box C2 |
FKHL14, LD, MFH-1, MFH1 |
Blepharoptosis, Cardiovascular abnormalities, Congenital musculoskeletal anomalies, Craniofacial abnormalities, Diabetes mellitus type 2, Distichiasis-lymphedema syndrome, Eyelid disease, Non-immune hydrops fetalis, Hypertension, Lymphedema, Obesity, Tetralogy of fallot |
4808
|
|
|
Forkhead box D2 |
FKHL17, FREAC-9, FREAC9 |
|
4809
|
|
|
Forkhead box D3 |
AIS1, Genesis, HFH2, VAMAS2 |
|
4810
|
|
|
Forkhead box D4 like 3 |
FOXD4B, FOXD4L2, FOXD4L4, FOXD6 |
|