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Congenital myopathy, Paradas type
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant limb-girdle muscular dystrophy type 1D
1 OMIM reference -
1 associated gene
No signs/symptoms info
Congenital myopathy, Paradas type
Autosomal dominant limb-girdle muscular dystrophy type 1D

DYSF
(UniProt - OMIM)
 DNAJB6
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
DYSF
(0.63)
DNAJB6


Citations in the biomedical literature:


Congenital myopathy, Paradas type
DYSF
Autosomal dominant limb-girdle muscular dystrophy type 1D
DNAJB6



Congenital myopathy, Paradas type
Autosomal dominant limb-girdle muscular dystrophy type 1D

Synonym(s):
(no synonyms)

Synonym(s):
- LGMD1D
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: adulthood
Average age of death: no data available
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.