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 |