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ZASP-related myofibrillar myopathy
1 OMIM reference -
1 associated gene
4 connected diseases
No signs/symptoms info
Disease Type of connection
Familial isolated dilated cardiomyopathy
Left ventricular noncompaction
Congenital analbuminemia
Muscular dystrophy, Selcen type
Synonym(s):
- Distal myopathy, Markesbery-Griggs type
- Myopathie distale type Markesbery-Griggs
- ZASPopathy
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
LDB3 O75112605906
No signs/symptoms info available.