PKDCC

protein kinase domain containing, cytoplasmic
OMIM: 614150
PanelMode of inheritanceDetails
2 panels
R-numbers: R21, R412
Signed-off version 5.80
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Rhizomelic limb shortening with dysmorphic features, OMIM:618821
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 7.26
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Rhizomelic limb shortening with dysmorphic features, OMIM:618821