LIFR

LIF receptor alpha
OMIM: 151443
PanelMode of inheritanceDetails
2 panels
R-numbers: R21
Signed-off version 1.92
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Stuve-Wiedemann syndrome, Schwartz-Jampel type 2 syndrome
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 2.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Stuve-Wiedemann syndrome/Schwartz-Jampel type 2 syndrome 601559