IRF6

interferon regulatory factor 6
OMIM: 607199
PanelMode of inheritanceDetails
5 panels
R-numbers: R83
Signed-off version 7.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Popliteal pterygium syndrome 1 119500
Green
in Clefting
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 6.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Orofacial cleft 6, 608864, Cleft Lip with or without Cleft Palate, Orofacial Clefting with skeletal features, Cleft lip +/- palate- unilateral or bilateral, cleft palate, lip pits, VAN DER WOUDE SYNDROME 1, VWS1, POPLITEAL PTERYGIUM SYNDROME, PPS, Cleft palate
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.6
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
VAN DER WOUDE SYNDROME 119300, POPLITEAL PTERYGIUM SYNDROME 119500
R-numbers: R21, R412
Signed-off version 4.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
POPLITEAL PTERYGIUM SYNDROME, VAN DER WOUDE SYNDROME
R-numbers: R284
Signed-off version 1.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes