Catalog

Limb-girdle muscular dystrophy 1H, gene mapped to 3p25.1p23

No MMS code

Link to WHO Definition

Limb-girdle muscular dystrophy 1H, gene mapped to 3p25.1p23 – http://id.who.int/icd/entity/320673324

Limb-girdle muscular dystrophy type 1H (LGMD1H) is an autosomal dominant disorder characterised by adult onset of progressive proximal muscle weakness affecting both the upper and lower limbs. A candidate disease locus, within a 25-cM region on chromosome 3p25.1-p23, has been identified.