SIN3A

SIN3 transcription regulator family member A
OMIM: 607776
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R29
Signed-off version 3.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Witteveen-Kolk syndrome, 613406, Syndromic intellectual disability