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Autosomal recessive limb-girdle muscular dystrophy type 2J
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Congenital myopathy, Paradas type
1 associated gene
No signs/symptoms info
Autosomal recessive limb-girdle muscular dystrophy type 2J
Congenital myopathy, Paradas type

TTN
(UniProt - OMIM)
 DYSF
(UniProt - OMIM)

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


Citations in the biomedical literature:


Autosomal recessive limb-girdle muscular dystrophy type 2J
TTN
Congenital myopathy, Paradas type
DYSF



Autosomal recessive limb-girdle muscular dystrophy type 2J
Congenital myopathy, Paradas type

Synonym(s):
- LGMD2J
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:
(no data available)
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.