| Preferred Name |
MERRF Syndrome |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84889 |
| code |
C84889 |
| DEFINITION |
A very rare mitochondrial abnormality characterized by myoclonic epilepsy and the microscopic finding of ragged-red fibers in muscle tissues. |
| label |
MERRF Syndrome |
| Preferred_Name |
MERRF Syndrome |
| prefixIRI |
C84889 |
| prefLabel |
MERRF Syndrome |
| Semantic_Type |
Disease or Syndrome |
| UMLS_CUI |
C0162672 |
| subClassOf |