|
411
|
|
|
Forkhead box H1 |
FAST-1, FAST1 |
Agenesis of corpus callosum, Alobar holoprosencephaly, Ambiguous genitalia, Asthma, Choanal atresia, Ciliopathies, Colorectal cancer, Congenital coloboma of iris, Congenital hypoplasia of penis, Cyclocephaly, Duodenal atresia, Dwarfism, Fused incisors, Hemangioma, Holoprosencephaly, Hypothyroidism, Lobar holoprosencephaly, Mental retardation, Microcephaly, Microform holoprosencephaly, Midline interhemispheric variant of holoprosencephaly, Panhypopituitarism, Renal agenesis, Scoliosis, Semilobar holoprosencephaly, Septopreoptic holoprosencephaly, Strabismus, Tetralogy of fallotView all (13 more) |
|
412
|
|
|
Fetal and adult testis expressed 1 |
CT43, FATE |
|
|
413
|
|
|
F2R like thrombin or trypsin receptor 3 |
PAR4 |
|
|
414
|
|
|
Family with sequence similarity 181 member A |
C14orf152 |
|
|
415
|
|
|
FERM domain containing 7 |
NYS, NYS1, XIPAN |
|
|
416
|
|
|
Family with sequence similarity 110 member B |
C8orf72 |
|
|
417
|
|
|
Fc gamma receptor IIc (gene/pseudogene) |
CD32, CD32C, CDW32, FCG2, FCRIIC, FcgammaRIIc, IGFR2 |
|
|
418
|
|
|
FGF1 intracellular binding protein |
FGFIBP, FIBP-1, TROFAS |
Ankylosing spondylitis, Cholangitis, Facial dysmorphism, Congenital epicanthus, Congenital ocular coloboma, Crohn disease, Developmental delay, Learning disorders, Macroglossia, Macrotia, Malrotation of kidney, Mental retardation, Mitral valve prolapse, Psoriasis, Strabismus, Thauvin-robinet-faivre syndrome, Ulcerative colitis, Vulval varicesView all (3 more) |
|
419
|
|
|
Family with sequence similarity 114 member A1 |
Noxp20 |
|
|
420
|
|
|
F-box protein 44 |
FBG3, FBX30, FBX6A, Fbx44, Fbxo6a |
|
