Mitochondrial neurogastrointestinal encephalomyopathy
MONDO:0017575A syndrome characterized by the association of gastrointestinal dysmotility, peripheral neuropathy, chronic progressive external ophthalmoplegia and leukoencephalopathy.
Also known as: MNGIE, Mitochondrial Neurogastrointestinal Encephalopathy, Mitochondrial neurogastrointestinal encephalopathy, mitochondrial Neurogastrointestingal encephalopathy, MNGIE syndrome, OGIMD, POLIP, mitochondrial neurogastrointestinal encephalopathy syndrome
27 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Broader categories
Disease
(680)
Metabolic disease
(233)
Nervous system disorder
(231)
Musculoskeletal system disorder
(207)
Hereditary disease
(176)
Peripheral nervous system disorder
(114)
Neuromuscular disease
(106)
Peripheral neuropathy
(91)
Inborn mitochondrial metabolism disorder
(58)
Muscle tissue disorder
(56)