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Rippling muscle disease
2 OMIM references -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Autosomal dominant limb-girdle muscular dystrophy type 1C
1 OMIM reference -
1 associated gene
No signs/symptoms info
Rippling muscle disease
Autosomal dominant limb-girdle muscular dystrophy type 1C

CAV3
(UniProt - OMIM)
 CAV3
(UniProt - OMIM)

COMMON
GENES 		CAV3


Citations in the biomedical literature:


Rippling muscle disease
CAV3
Autosomal dominant limb-girdle muscular dystrophy type 1C



Rippling muscle disease
Autosomal dominant limb-girdle muscular dystrophy type 1C

Synonym(s):
(no synonyms)

Synonym(s):
- LGMD1C
- Limb-girdle muscular dystrophy due to caveolin-3 deficiency
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:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
1 MeSH reference: C535685
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.