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MERRF syndrome

Disease Summary
Associated Targets (4)
Tclin

2

Tchem

1

Tbio

1


Explore Associated Targets
Mondo Description A condition that can be caused by mutation(s) in more than one mitochondrial gene. It is characterized by myoclonic epilepsy and ragged-red fibers present on muscle biopsy.
Mondo Term and Equivalent IDs
MONDO:0010790:  MERRF syndrome
GARD:0007144: 
ICD10:E88.42: 
MESH:D017243: 
NCIT:C84889: 
Orphanet:551: 
SCTID:68448003: 
UMLS:C0162672: 
GWAS Targets (0)
No GWAS traits found
Disease Hierarchy
Target Novelty (Tin-x)