MERRF syndrome
Information
- Disease name
- MERRF syndrome
- Disease ID
- DOID:310
- Description
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT05554835 | Recruiting | Global Registry and Natural History Study for Mitochondrial Disorders | February 1, 2009 | December 2040 |
- Disase is a (Disease Ontology)
- DOID:890
- Cross Reference ID (Disease Ontology)
- ICD10CM:E88.42
- Cross Reference ID (Disease Ontology)
- MESH:D017243
- Cross Reference ID (Disease Ontology)
- MIM:545000
- Cross Reference ID (Disease Ontology)
- NCI:C84889
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:68448003
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0162672
- Exact Synonym (Disease Ontology)
- Fukuhara syndrome
- Exact Synonym (Disease Ontology)
- Myoclonic epilepsy - ragged red fibers
- Exact Synonym (Disease Ontology)
- Myoclonus epilepsy AND ragged red fibers
- Exact Synonym (Disease Ontology)
- Myoclonus with epilepsy and with Ragged Red Fibers
- MeSH unique ID (MeSH (Medical Subject Headings))
- D017243