mitochondrial myopathy
myopathy characterized by mitochondrial dysfunction
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mitochondrial myopathy
Summary
mitochondrial myopathy is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[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 is a type of muscular disease[5].
- mitochondrial myopathy is a type of mitochondrial disease[6].
- mitochondrial myopathy is a type of rare genetic developmental defect during embryogenesis[7].
- mitochondrial myopathy is a type of disease[8].
- mitochondrial myopathy's Commons category is recorded as Mitochondrial myopathy[9].
- mitochondrial myopathy's NCI Thesaurus ID is recorded as C101328[10].
- mitochondrial myopathy's health specialty is recorded as neurology[11].
- mitochondrial myopathy's genetic association is recorded as MSTO1[12].
- mitochondrial myopathy's genetic association is recorded as FDX2[13].
- mitochondrial myopathy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_699[14].
- mitochondrial myopathy's exact match is recorded as http://identifiers.org/doid/DOID:699[15].
- mitochondrial myopathy's exact match is recorded as http://purl.obolibrary.org/obo/HP_0003737[16].
- mitochondrial myopathy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_206966[17].
- mitochondrial myopathy's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
Why It Matters
mitochondrial myopathy has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2] It is known by 5 alternative names across languages and contexts.[19]