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Autosomal recessive limb-girdle muscular dystrophy type 2J
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Hereditary proximal myopathy with early respiratory failure
1 OMIM reference -
1 associated gene
No signs/symptoms info
Autosomal recessive limb-girdle muscular dystrophy type 2J
Hereditary proximal myopathy with early respiratory failure

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

COMMON
GENES 		TTN


Citations in the biomedical literature:


Autosomal recessive limb-girdle muscular dystrophy type 2J
TTN
Hereditary proximal myopathy with early respiratory failure



Autosomal recessive limb-girdle muscular dystrophy type 2J
Hereditary proximal myopathy with early respiratory failure

Synonym(s):
- LGMD2J
Synonym(s):
- ADMERF
- Edström Myopathy
- HIBM-ERF
- Hereditary inclusion body myopathy with early respiratory failure
- Myofibrillar myopathy with early respiratory failure
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 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.