mitochondrial myopathy

Summary

mitochondrial myopathy is a developmental defect during embryogenesis^[1]. It draws 74 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #72 of 308).^[2]

Key Facts

• mitochondrial myopathy's instance of is recorded as developmental defect during embryogenesis^[3].
• mitochondrial myopathy's instance of is recorded as class of disease^[4].
• mitochondrial myopathy's subclass of is recorded as muscular disease^[5].
• mitochondrial myopathy's subclass of is recorded as mitochondrial disease^[6].
• mitochondrial myopathy's subclass of is recorded as rare genetic developmental defect during embryogenesis^[7].
• mitochondrial myopathy's subclass of is recorded as disease^[8].
• mitochondrial myopathy's Commons category is recorded as Mitochondrial myopathy^[9].
• mitochondrial myopathy's MeSH descriptor ID is recorded as D017240^[10].
• mitochondrial myopathy's OMIM ID is recorded as 251900^[11].
• mitochondrial myopathy's ICD-10 ID is recorded as G71.3^[12].
• mitochondrial myopathy's Freebase ID is recorded as /m/02p70sz^[13].
• mitochondrial myopathy's MeSH tree code is recorded as C05.651.460^[14].
• mitochondrial myopathy's MeSH tree code is recorded as C10.668.491.500^[15].
• mitochondrial myopathy's MeSH tree code is recorded as C18.452.660.560^[16].
• mitochondrial myopathy's Disease Ontology ID is recorded as DOID:699^[17].
• mitochondrial myopathy's Encyclopædia Britannica Online ID is recorded as topic/mitochondrial-myopathy^[18].
• mitochondrial myopathy's Orphanet ID is recorded as 206966^[19].
• mitochondrial myopathy's NCI Thesaurus ID is recorded as C101328^[20].
• mitochondrial myopathy's health specialty is recorded as neurology^[21].
• mitochondrial myopathy's genetic association is recorded as MSTO1^[22].
• mitochondrial myopathy's genetic association is recorded as FDX2^[23].
• mitochondrial myopathy's BabelNet ID is recorded as 02223010n^[24].
• mitochondrial myopathy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_699^[25].
• mitochondrial myopathy's exact match is recorded as http://identifiers.org/doid/DOID:699^[26].
• mitochondrial myopathy's exact match is recorded as http://purl.obolibrary.org/obo/HP_0003737^[27].

Why It Matters

mitochondrial myopathy draws 74 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #72 of 308).^[2] It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.^[28] It is known by 5 alternative names across languages and contexts.^[29]