MERRF syndrome
mitochondrial disease
Press Enter · cited answer in seconds
0 sources
MERRF syndrome
Summary
MERRF syndrome is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 14 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- MERRF syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- MERRF syndrome's instance of is recorded as class of disease[4].
- MERRF syndrome is a type of mitochondrial encephalomyopathy[5].
- MERRF syndrome is a type of mitochondrial oxidative phosphorylation disorder due to a point mutation of mitochondrial DNA[6].
- MERRF syndrome is a type of neurometabolic disease[7].
- MERRF syndrome is a type of mitochondrial disease with epilepsy[8].
- MERRF syndrome is a type of mitochondrial disease with peripheral neuropathy[9].
- MERRF syndrome is a type of syndrome associated with hypertrophic cardiomyopathy[10].
- MERRF syndrome is a type of mitochondrial disease with eye involvement[11].
- MERRF syndrome is a type of mitochondrial disease with hypertrophic cardiomyopathy[12].
- MERRF syndrome is a type of mitochondrial disease with dilated cardiomyopathy[13].
- MERRF syndrome is a type of disease[14].
- MERRF syndrome's ICD-9-CM is recorded as 277.87[15].
- MERRF syndrome's NCI Thesaurus ID is recorded as C84889[16].
- MERRF syndrome's health specialty is recorded as neurology[17].
- MERRF syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_310[18].
- MERRF syndrome's exact match is recorded as http://identifiers.org/doid/DOID:310[19].
- MERRF syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_551[20].
- MERRF syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[21].
Why It Matters
MERRF syndrome has Wikipedia articles in 14 language editions, a strong signal of global cultural recognition.[2] It is known by 24 alternative names across languages and contexts.[22]