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Duchenne muscular dystrophy

MONDO:0010679

Also known as: DMD, Duchenne muscular dystrophy, Duchenne muscular dystrophy, X-linked recessive, severe dystrophinopathy, Duchenne type, muscular dystrophy, Duchenne type

MONDO:
MONDO:0010679
Orphanet:
98896 ↗
OMIM:
310200 ↗
Rare disease51 associated genes

Description

Duchenne muscular dystrophy (DMD) is a neuromuscular disease characterized by rapidly progressive muscle weakness and wasting due to degeneration of skeletal, smooth and cardiac muscle.

Associated genes

+41 more genes — install the extension to see the full list inline on any page.

External references

Sources: MONDO (CC BY 4.0), Open Targets (CC0), Orphanet (CC BY 4.0).

Not for sole clinical decision-making. Always verify against primary sources.

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