TM2D3

TM2 domain containing 3
OMIM: 610014
PanelMode of inheritanceDetails
1 panel
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 7.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
MONDO:0700092, TM2D3-related neurodevelopmental disorder with microcephaly and congenital malformations