HIST1H1E

histone cluster 1 H1 family member e
OMIM: 142220
PanelMode of inheritanceDetails
2 panels
R-numbers: R21, R412
Signed-off version 2.4
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Rahman syndrome, OMIM:617537, Rahman syndrome, MONDO:0044323
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R29
Signed-off version 4.4
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Rahman syndrome, 617537, mild to severe intellectual disability