ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

2 OMIM references -
1 associated gene
No signs/symptoms info

Autosomal dominant limb-girdle muscular dystrophy type 1C

Rippling muscle disease

CAV3

Citations in the biomedical literature:

Autosomal dominant limb-girdle muscular dystrophy type 1C		Rippling muscle disease
	Synonym(s): - LGMD1C - Limb-girdle muscular dystrophy due to caveolin-3 deficiency		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 1 OMIM reference - No MeSH references		External references: 2 OMIM references - 1 MeSH reference: C535685

No signs/symptoms info available.