Medical Subject Headings

Last uploaded: November 5, 2019
Preferred Name

Muscular Dystrophy, Oculopharyngeal

Synonyms

Dystrophies, Oculopharyngeal Muscular

Definitions

An autosomal dominant hereditary disease that presents in late in life and is characterized by DYSPHAGIA and progressive ptosis of the eyelids. Mutations in the gene for POLY(A)-BINDING PROTEIN II have been associated with oculopharyngeal muscular dystrophy.

ID

http://purl.bioontology.org/ontology/MESH/D039141

altLabel

Dystrophies, Oculopharyngeal Muscular

Oculopharyngeal Muscular Dystrophies

Oculopharyngeal Muscular Dystrophy

Dystrophy, Oculopharyngeal Muscular

Oculopharyngeal Dystrophy

Progressive Muscular Dystrophy, Oculopharyngeal Type

Muscular Dystrophies, Oculopharyngeal

AN

/vet: coord with MUSCULAR DYSTROPHY, ANIMAL

AQL

BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI

cui

C0270952

DC

1

definition

An autosomal dominant hereditary disease that presents in late in life and is characterized by DYSPHAGIA and progressive ptosis of the eyelids. Mutations in the gene for POLY(A)-BINDING PROTEIN II have been associated with oculopharyngeal muscular dystrophy.

DX

20030101

FX

D039103

HN

2003; use MUSCULAR DYSTROPHIES 2001-2002

Inverse of AQ

http://purl.bioontology.org/ontology/MESH/Q000401

http://purl.bioontology.org/ontology/MESH/Q000150

http://purl.bioontology.org/ontology/MESH/Q000188

http://purl.bioontology.org/ontology/MESH/Q000517

http://purl.bioontology.org/ontology/MESH/Q000201

http://purl.bioontology.org/ontology/MESH/Q000145

http://purl.bioontology.org/ontology/MESH/Q000503

http://purl.bioontology.org/ontology/MESH/Q000453

http://purl.bioontology.org/ontology/MESH/Q000208

http://purl.bioontology.org/ontology/MESH/Q000134

http://purl.bioontology.org/ontology/MESH/Q000821

http://purl.bioontology.org/ontology/MESH/Q000382

http://purl.bioontology.org/ontology/MESH/Q000601

http://purl.bioontology.org/ontology/MESH/Q000235

http://purl.bioontology.org/ontology/MESH/Q000523

http://purl.bioontology.org/ontology/MESH/Q000276

http://purl.bioontology.org/ontology/MESH/Q000191

http://purl.bioontology.org/ontology/MESH/Q000652

http://purl.bioontology.org/ontology/MESH/Q000662

http://purl.bioontology.org/ontology/MESH/Q000151

http://purl.bioontology.org/ontology/MESH/Q000628

http://purl.bioontology.org/ontology/MESH/Q000196

http://purl.bioontology.org/ontology/MESH/Q000534

http://purl.bioontology.org/ontology/MESH/Q000266

http://purl.bioontology.org/ontology/MESH/Q000532

http://purl.bioontology.org/ontology/MESH/Q000139

http://purl.bioontology.org/ontology/MESH/Q000378

http://purl.bioontology.org/ontology/MESH/Q000175

http://purl.bioontology.org/ontology/MESH/Q000000981

http://purl.bioontology.org/ontology/MESH/Q000097

http://purl.bioontology.org/ontology/MESH/Q000473

http://purl.bioontology.org/ontology/MESH/Q000451

http://purl.bioontology.org/ontology/MESH/Q000209

http://purl.bioontology.org/ontology/MESH/Q000178

http://purl.bioontology.org/ontology/MESH/Q000469

Inverse of RO

http://purl.bioontology.org/ontology/MESH/D039103

Inverse of SIB

http://purl.bioontology.org/ontology/MESH/D020389

http://purl.bioontology.org/ontology/MESH/D006014

http://purl.bioontology.org/ontology/MESH/D049310

http://purl.bioontology.org/ontology/MESH/D020391

http://purl.bioontology.org/ontology/MESH/D020388

http://purl.bioontology.org/ontology/MESH/D058494

http://purl.bioontology.org/ontology/MESH/D049288

http://purl.bioontology.org/ontology/MESH/D009223

Machine permutation

2003; see MUSCULAR DYSTROPHIES 2001-2002

Mapped from

http://purl.bioontology.org/ontology/MESH/C536350

MDA

20020703

MMR

20130708

MN

C16.320.577.450

C05.651.534.500.450

C10.668.491.175.500.450

notation

D039141

prefLabel

Muscular Dystrophy, Oculopharyngeal

TERMUI

T812267

T842184

T369181

T842183

TH

NLM (2000)

ORD (2010)

OMIM (2013)

GHR (2014)

tui

T047

subClassOf

http://purl.bioontology.org/ontology/MESH/D009136

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http://purl.bioontology.org/ontology/OMIM/602279 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/164300 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/ICD10CM/G71.0 International Classification of Diseases, Version 10 - Clinical Modification CUI