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Hyaline body myopathy
2 OMIM references -
1 associated gene
8 connected diseases
No signs/symptoms info
Disease Type of connection
Classic multiminicore myopathy
Ebstein malformation
Familial isolated dilated cardiomyopathy
Laing distal myopathy
Left ventricular noncompaction
Helicoid peripapillary chorioretinal degeneration
46,XY partial gonadal dysgenesis
Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
External references:
2 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
MYH7 P12883160760
No signs/symptoms info available.