TWIST2

twist family bHLH transcription factor 2
OMIM: 607556
PanelMode of inheritanceDetails
2 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
ABLEPHARON MACROSTOMIA SYNDROME, OMIM:200110, Focal facial dermal dysplasia 3, Setleis type, OMIM:227260
R-numbers: R21, R412
Signed-off version 2.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Ablepharon-macrostomia syndrome, 200110, Barber-Say syndrome, 209885