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Autosomal dominant limb-girdle muscular dystrophy type 1A
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Myotilin-related myofibrillar myopathy without spheroid body
1 OMIM reference -
1 associated gene
No signs/symptoms info
Autosomal dominant limb-girdle muscular dystrophy type 1A
Myotilin-related myofibrillar myopathy without spheroid body

MYOT
(UniProt - OMIM)
 MYOT
(UniProt - OMIM)

COMMON
GENES 		MYOT


Citations in the biomedical literature:


Autosomal dominant limb-girdle muscular dystrophy type 1A
MYOT
Myotilin-related myofibrillar myopathy without spheroid body



Autosomal dominant limb-girdle muscular dystrophy type 1A
Myotilin-related myofibrillar myopathy without spheroid body

Synonym(s):
- LGMD1A
- Limb-girdle muscular dystrophy due to myotilin deficiency
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:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.