HR

HR, lysine demethylase and nuclear receptor corepressor
OMIM: 602302
PanelMode of inheritanceDetails
3 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
ALOPECIA UNIVERSALIS 146550, ATRICHIA WITH PAPULAR LESIONS 209500
R-numbers: R163
Signed-off version 2.1
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Marie Unna hereditary hypotrichosis (MUHH), Alopecia universalis, OMIM:203655, Atrichia with papular lesions, OMIM:209500
R-numbers: R21, R412
Signed-off version 2.4
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
ATRICHIA WITH PAPULAR LESIONS, ALOPECIA UNIVERSALIS