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2 OMIM references -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Hyaline body myopathy
Laing distal myopathy

MYH7 MYH7


COMMON
GENES
MYH7



Citations in the biomedical literature:


Hyaline body myopathy
MYH7
Laing distal myopathy



Hyaline body myopathy
Laing distal myopathy

Synonym(s):
(no synonyms)

Synonym(s):
- Distal myopathy type 1
- Laing early-onset distal myopathy
- MPD1

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: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
2 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.