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Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia
1 associated gene
No signs/symptoms info
Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia

MYH2
(UniProt - OMIM)
 MYH2
(UniProt - OMIM)

COMMON
GENES 		MYH2


Citations in the biomedical literature:


Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia
MYH2
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia



Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia

Synonym(s):
- HIBM3
- Hereditary inclusion body myopathy type 3
- IBM3
- Inclusion body myopathy type 3
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare eye disease
- 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: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
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
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.