MeSH Browser

MeSH Supplementary: Visceral myopathy familial external ophthalmoplegia
Unique ID: C536350
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536350
Entry Term(s): Intestinal pseudoobstruction with external ophthalmoplegia; MNGIE Disease; MNGIE Syndrome; Mitochondrial DNA Depletion Syndrome 1; Mitochondrial DNA Depletion Syndrome 8A; Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form, With Renal Tubulopathy, Autosomal Recessive; Mitochondrial Myopathy with Sensorimotor Polyneuropathy, Ophthalmoplegia, and Pseudo-Obstruction; Mitochondrial Neurogastrointestinal Encephalopathy Disease; Mitochondrial Neurogastrointestinal Encephalopathy Syndrome, Rrm2b-Related; Mitochondrial neurogastrointestinal encephalopathy syndrome; Mngie Without Leukoencephalopathy; Mngie, Rrm2b-Related; Muscular dystrophy, oculogastrointestinal; Myoneurogastrointestinal encephalopathy syndrome; Oculogastrointestinal Muscular Dystrophy; POLIP Syndrome; Polyneuropathy, Ophthalmoplegia, Leukoencephalopathy, and Intestinal Pseudo-Obstruction; Polyneuropathy, ophthalmoplegia, leukoencephalopathy, and intestinal pseudoobstruction; Thymidine Phosphorylase Deficiency; Visceral Myopathy, Familial, With External Ophthalmoplegia
Registry Numbers: 0
Heading Mapped to: *Intestinal Pseudo-Obstruction; Ophthalmoplegia / congenital; *Muscular Dystrophy, Oculopharyngeal
Frequency: 88
Date of Entry: 2010/08/25
Revision Date: 2020/02/28

Visceral myopathy familial external ophthalmoplegia MeSH Supplementary Concept Data 2025