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Autosomal dominant limb-girdle muscular dystrophy type 1C
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Muscle-eye-brain disease with bilateral multicystic leucodystrophy
1 associated gene
No signs/symptoms info
Autosomal dominant limb-girdle muscular dystrophy type 1C
Muscle-eye-brain disease with bilateral multicystic leucodystrophy

CAV3
(UniProt - OMIM)
 DAG1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CAV3
(0.85)
DAG1


Citations in the biomedical literature:


Autosomal dominant limb-girdle muscular dystrophy type 1C
CAV3
Muscle-eye-brain disease with bilateral multicystic leucodystrophy
DAG1



Autosomal dominant limb-girdle muscular dystrophy type 1C
Muscle-eye-brain disease with bilateral multicystic leucodystrophy

Synonym(s):
- LGMD1C
- Limb-girdle muscular dystrophy due to caveolin-3 deficiency
Synonym(s):
- MEB disease with bilateral multicystic leucodystrophy
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- 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:
No OMIM references
No MeSH references
No signs/symptoms info available.