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Laing distal myopathy
1 OMIM reference -
1 associated gene
8 connected diseases
No signs/symptoms info
Disease Type of connection
Classic multiminicore myopathy
Ebstein malformation
Familial isolated dilated cardiomyopathy
Hyaline body myopathy
Left ventricular noncompaction
Helicoid peripapillary chorioretinal degeneration
46,XY partial gonadal dysgenesis
Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit
Synonym(s):
- Distal myopathy type 1
- Laing early-onset distal myopathy
- MPD1
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
MYH7 P12883160760
No signs/symptoms info available.