mitochondrial neurogastrointestinal encephalomyopathy
Mitochondrial NeuroGastroIntestinal Encephalomyopathy (MNGIE) syndrome is characterized by the association of gastrointestinal dysmotility, peripheral neuropathy, chronic progressive external ophthalmoplegia and leukoencephalopathy
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mitochondrial neurogastrointestinal encephalomyopathy
Summary
mitochondrial neurogastrointestinal encephalomyopathy is a class of disease[1].
Key Facts
- mitochondrial neurogastrointestinal encephalomyopathy's instance of is recorded as class of disease[2].
- mitochondrial neurogastrointestinal encephalomyopathy's subclass of is recorded as mitochondrial myopathy[3].
- mitochondrial neurogastrointestinal encephalomyopathy's MeSH descriptor ID is recorded as C537477[4].
- mitochondrial neurogastrointestinal encephalomyopathy's KEGG ID is recorded as H01390[5].
- mitochondrial neurogastrointestinal encephalomyopathy's Orphanet ID is recorded as 298[6].
- mitochondrial neurogastrointestinal encephalomyopathy's NCI Thesaurus ID is recorded as C119678[7].
- mitochondrial neurogastrointestinal encephalomyopathy's genetic association is recorded as TYMP[8].
- mitochondrial neurogastrointestinal encephalomyopathy's genetic association is recorded as RRM2B[9].
- mitochondrial neurogastrointestinal encephalomyopathy's genetic association is recorded as POLG[10].
- mitochondrial neurogastrointestinal encephalomyopathy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_298[11].
- mitochondrial neurogastrointestinal encephalomyopathy's UMLS CUI is recorded as C0872218[12].
- mitochondrial neurogastrointestinal encephalomyopathy's ICD-10-CM is recorded as G71.3[13].
- mitochondrial neurogastrointestinal encephalomyopathy's GARD rare disease ID is recorded as 9920[14].
- mitochondrial neurogastrointestinal encephalomyopathy's Mondo ID is recorded as MONDO_0017575[15].