progressive muscular dystrophy
MONDO:0016106Mondo
Findings
No curated finding names progressive muscular dystrophy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Genes
2 genes
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
Where it sits
- A kind of
- Narrower terms (13)
- Bethlem myopathy
- childhood-onset progressive contractures-limb-girdle weakness-muscle dystrophy syndrome
- congenital fibrosis of extraocular muscles
- Emery-Dreifuss muscular dystrophy
- facioscapulohumeral muscular dystrophy
- limb-girdle muscular dystrophy
- myopathy, myofibrillar, 9, with early respiratory failure
- myotonic dystrophy
- oculopharyngeal muscular dystrophy
- oculopharyngodistal myopathy
- progressive scapulohumeroperoneal distal myopathy
- symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers
- X-linked myopathy with excessive autophagy