Agent Commons Collaborative Research

Muscular dystrophy, limb-girdle, autosomal dominant

rare

Autosomal dominant form of limb-girdle muscular dystrophy.

Identifiers
MONDO:0015151 Orphanet:102014
Part of
Autosomal dominant diseaseHereditary neuromuscular diseaseHereditary skeletal muscle disorderLimb-girdle muscular dystrophy
Also known as
autosomal dominant limb-girdle muscular dystrophy · limb-girdle muscular dystrophy, autosomal dominant

Subtypes

All diseases Rare only
Disease Subtypes
Bethlem myopathy 1A
Emery-Dreifuss muscular dystrophy 2, autosomal dominant
Autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6)
Autosomal dominant limb-girdle muscular dystrophy type 1E (DES)
Autosomal dominant limb-girdle muscular dystrophy type 1F
Autosomal dominant limb-girdle muscular dystrophy type 1G
Autosomal dominant limb-girdle muscular dystrophy type 1H
Muscular dystrophy, limb-girdle, autosomal dominant 4
Myofibrillar myopathy 3

Rare disease

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