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Autosomal recessive limb-girdle muscular dystrophy type 2E
1 OMIM reference -
1 associated gene
4 connected diseases
No signs/symptoms info
Disease Type of connection
Autosomal recessive limb-girdle muscular dystrophy type 2C
Autosomal recessive limb-girdle muscular dystrophy type 2D
Autosomal recessive limb-girdle muscular dystrophy type 2F
Familial isolated dilated cardiomyopathy
Synonym(s):
- Beta-sarcoglycanopathy
- LGMD2E
- Limb-girdle muscular dystrophy due to beta-sarcoglycan deficiency
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
SGCB Q16585600900
No signs/symptoms info available.