WDR11

WD repeat domain 11
OMIM: 606417
PanelMode of inheritanceDetails
3 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
KALLMANN SYNDROME
R-numbers: R148
Signed-off version 2.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Hypogonadotropic hypogonadism type 14 (OMIM 614858)
R-numbers: R88
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Intellectual disability, MONDO:0001071, Microcephaly, MONDO:0001149, Short stature,HP:0004322