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Autosomal dominant limb-girdle muscular dystrophy type 1E
ORPHA:34517
- Synonym(s):
- LGMD1E
- Prevalence: -
- Inheritance: -
- Age of onset: -
- ICD-10: G71.8
- OMIM: -
- UMLS: C3148763
- MeSH: -
- GARD: 12529
- MedDRA: -
Summary
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Desminopathy
Additional information
Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
Specialised Social Services
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