ZMYM2

zinc finger MYM-type containing 2
OMIM: 602221
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 5.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities, OMIM:619522