CCT3

chaperonin containing TCP1 subunit 3
OMIM: 600114
PanelMode of inheritanceDetails
1 panel
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 5.48
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CCT3-related neurodevelopmental disorder with hypomyelination of white matter, OMIM:621034