SGCG

sarcoglycan gamma
OMIM: 608896
PanelMode of inheritanceDetails
2 panels
R-numbers: R21, R412
Signed-off version 2.4
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Muscular dystrophy, limb-girdle, autosomal recessive 5, OMIM:253700, Autosomal recessive limb-girdle muscular dystrophy type 2C, MONDO:0009677
Component of the following Super Panels:
  • - Hypotonic infant
  • - Neuromuscular disorders
R-numbers: R82
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Limb-Girdle Muscular Dystrophy, Recessive, Muscular dystrophy, limb-girdle, type 2C, 253700, Limb-girdle muscular dystrophy