Orphanet Rare Disease Ontology

Last uploaded: July 3, 2024
Preferred Name

Polymyositis
Synonyms
Definitions

A rare idiopathic inflammatory myopathy (IIM) historically characterized by symmetric proximal muscle weakness, elevated muscle enzymes (creatine kinase), myopathic findings on electromyography, and muscle biopsy showing endomyial infiltration composed mainly of macrophages and lymphocytes. The features are non-specific, thus the disease should be distinguished from similar entities with specific clinical, immunological, histological features, notably dermatomyositis, immune-mediated necrotizing myopathy, anti-synthetase syndrome, inclusion body myositis, and myositis associated with other connective tissue disorder.

ID

http://www.orpha.net/ORDO/Orphanet_732

definition

A rare idiopathic inflammatory myopathy (IIM) historically characterized by symmetric proximal muscle weakness, elevated muscle enzymes (creatine kinase), myopathic findings on electromyography, and muscle biopsy showing endomyial infiltration composed mainly of macrophages and lymphocytes. The features are non-specific, thus the disease should be distinguished from similar entities with specific clinical, immunological, histological features, notably dermatomyositis, immune-mediated necrotizing myopathy, anti-synthetase syndrome, inclusion body myositis, and myositis associated with other connective tissue disorder.

definition_citation

Orphanet

expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=732

has_age_of_onset

Adult

Elderly

has_inheritance

Not applicable

hasDbXref

MedDRA:10036102

ICD-11:4A41.1

MeSH:D017285

ICD-10:M33.2

UMLS:C0085655

label

Polymyositis

notation

ORPHA:732

part_of

http://www.orpha.net/ORDO/Orphanet_98482

http://www.orpha.net/ORDO/Orphanet_567558

prefixIRI

ORDO:Orphanet_732

prefLabel

Polymyositis

present_in

Australia AND has_point_prevalence_average_value : 7.2 AND has_point_prevalence_range : 1-9 / 100 000

Spain AND has_annual_incidence_average_value : 0.39 AND has_annual_incidence_range : 1-9 / 1 000 000

Sweden AND has_annual_incidence_average_value : 0.76 AND has_annual_incidence_range : 1-9 / 1 000 000

Argentina AND has_annual_incidence_average_value : 0.75 AND has_annual_incidence_range : 1-9 / 1 000 000

Argentina AND has_point_prevalence_average_value : 7.2 AND has_point_prevalence_range : 1-9 / 100 000

Europe AND has_annual_incidence_average_value : 0.585 AND has_annual_incidence_range : 1-9 / 1 000 000

Europe AND has_point_prevalence_average_value : 7.1 AND has_point_prevalence_range : 1-9 / 100 000

Australia AND has_annual_incidence_average_value : 0.41 AND has_annual_incidence_range : 1-9 / 1 000 000

treeView

http://www.orpha.net/ORDO/Orphanet_98482

http://www.orpha.net/ORDO/Orphanet_567558

subClassOf

http://www.orpha.net/ORDO/Orphanet_377788

http://www.orpha.net/ORDO/Orphanet_557493

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Delete Mapping To Ontology Source
http://www.radlex.org/RID/RID3654 RADLEX LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU037341 OMIM LOOM
http://purl.bioontology.org/ontology/ICD9CM/710.4 ICD9CM LOOM
http://purl.bioontology.org/ontology/MESH/D017285 MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D017285 RH-MESH LOOM
http://purl.bioontology.org/ontology/MEDDRA/10036102 MEDDRA LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Polymyositis CSEO LOOM
http://purl.bioontology.org/ontology/SNMI/D1-10320 SNMI LOOM
http://www.ebi.ac.uk/efo/EFO_0003063 CCONT LOOM
http://www.ebi.ac.uk/efo/EFO_0003063 EFO LOOM
http://www.ebi.ac.uk/efo/EFO_0003063 EFO LOOM
http://www.co-ode.org/ontologies/galen#Polymyositis GALEN LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0085655 MEDLINEPLUS LOOM
https://github.com/sap218/coid/blob/master/coid.owl#COID_00562 COID LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0085655 OCHV LOOM
http://purl.bioontology.org/ontology/RCTV2/N004.00 RCTV2 LOOM
https://github.com/sap218/ocimido/blob/master/ontology/ocimido.owl#OCIMIDO_00073 OCIMIDO LOOM
http://www.semanticweb.org/ontologies/2012/5/Ontology1338526551855.owl#Polymyositis RPO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.668.491.562.575 RH-MESH LOOM
http://purl.obolibrary.org/obo/OMIT_0017666 OMIT LOOM
http://www.phoc.org.cn/pmo/class/PMO_00037745 PMAPP-PMO LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C26925 NCIT LOOM
http://purl.bioontology.org/ontology/WHO/1245 WHO-ART LOOM
http://purl.obolibrary.org/obo/DERMO_0001897 DERMO LOOM
http://purl.bioontology.org/ontology/ICD10/M33.2 ICD10 LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_10222 NATPRO LOOM
http://purl.obolibrary.org/obo/NCIT_C26925 BERO LOOM
rgo:03506 GAMUTS LOOM
http://purl.bioontology.org/ontology/ICPC2P/L99060 ICPC2P LOOM
http://purl.obolibrary.org/obo/MONDO_0019127 GCBO LOOM
http://purl.obolibrary.org/obo/MONDO_0019127 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0019127 DOVES LOOM
http://purl.obolibrary.org/obo/MONDO_0019127 KTAO LOOM
http://purl.obolibrary.org/obo/MONDO_0019127 OBA LOOM
http://nanbyodata.jp/ontology/NANDO_1200276 NANDO LOOM
http://localhost/plosthes.2017-1#7982 PLOSTHES LOOM
http://radlex.org/RID/RID3654 RADLEX LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#15712 OCHV LOOM
http://www.limics.org/hrdo/rdfns#pat_id_700 HRDO LOOM
http://purl.bioontology.org/ontology/RCD/N004. RCD LOOM
http://purl.bioontology.org/ontology/ICD10CM/M33.2 ICD10CM LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C05.651.594.819 RH-MESH LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/31384009 SNOMEDCT LOOM
http://purl.jp/bio/4/id/200906028228145651 IOBC LOOM
http://purl.bioontology.org/ontology/CSP/1982-9752 CRISP LOOM
http://purl.obolibrary.org/obo/DOID_0080745 DOID LOOM
http://purl.obolibrary.org/obo/DOID_0080745 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_0080745 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_0080745 MIDO LOOM
http://purl.obolibrary.org/obo/DOID_0080745 FNS-H LOOM
http://www.gamuts.net/entity#polymyositis GAMUTS REST