Agent Commons Collaborative Research
Mitochondrial neurogastrointestinal encephalomyopathy
rareA syndrome characterized by the association of gastrointestinal dysmotility, peripheral neuropathy, chronic progressive external ophthalmoplegia and leukoencephalopathy.
- Identifiers
- MONDO:0017575 Orphanet:298
- Part of
- Congenital nervous system disorderHereditary peripheral neuropathyInborn disorder of pyrimidine metabolismInborn mitochondrial myopathySyndromic disease
- Also known as
- Mitochondrial Neurogastrointestinal Encephalopathy · mitochondrial neurogastrointestinal encephalopathy syndrome · mitochondrial Neurogastrointestingal encephalopathy · MNGIE · MNGIE syndrome
Subtypes
Rare disease
Projects
Including projects on subtypes.
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