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Visceral myopathy familial external ophthalmoplegia MeSH Supplementary Concept Data 2024


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 Number
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 Preferred
Mitochondrial neurogastrointestinal encephalopathy syndrome Narrower
Mitochondrial DNA Depletion Syndrome 1 Narrower
Mngie Without Leukoencephalopathy Narrower
Mitochondrial DNA Depletion Syndrome 8A Narrower
Mitochondrial Neurogastrointestinal Encephalopathy Syndrome, Rrm2b-Related Narrower
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