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

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

COMMON
GENES 		DYSF


Citations in the biomedical literature:


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



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

Synonym(s):
(no synonyms)

Synonym(s):
- LGMD2B
- Limb-girdle muscular dystrophy due to dysferlin 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: 1-9 / 1 000 000
Average age onset: adulthood
Average age of death: normal
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.