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Autosomal recessive limb-girdle muscular dystrophy type 2L
1 OMIM reference -
1 associated gene
4 connected diseases
No signs/symptoms info
Disease Type of connection
Gnathodiaphyseal dysplasia
Miyoshi myopathy
Giant cell glioblastoma
Gliosarcoma
Synonym(s):
- LGMD2L
Classification (Orphanet):
- 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: adulthood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
ANO5 Q75V66608662
No signs/symptoms info available.