Autosomal recessive limb girdle muscular dystrophy type 2O

Autosomal recessive limb girdle muscular dystrophy type 2O (disorder)

active

Code	`725043006`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20170731

Synonyms

Limb-girdle muscular dystrophy 2O POMGNT1 (protein o-mannose beta-1,2-n-acetylglucosaminyltransferase) gene mutation
Limb-girdle muscular dystrophy 2O POMGNT1 gene mutation

Parents (1)

240054004Autosomal recessive muscular dystrophy with limb girdle distribution disorder

Children (0)

None (leaf concept).