PRKG2

protein kinase, cGMP-dependent, type II
OMIM: 601591
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Acromesomelic dysplasia 4, OMIM:619636, Spondylometaphyseal dysplasia, Pagnamenta type, OMIM:619638