Orphanet Rare Disease Ontology

Last uploaded: December 13, 2023
Preferred Name

Postpoliomyelitis syndrome

Synonyms

Postpoliomyelitic syndrome

Definitions

Postpoliomyelitis syndrome (PPS) is a neurologic disorder characterized by the development of new neuromuscular symptoms such as progressive muscular weakness or abnormal muscle fatigability occurring in survivors of the acute paralytic form of poliomyelitis (see this term), 15-40 years after recovery from the disease, and that is unexplained by other medical causes. Other manifestations that can occur gradually include generalized fatigue, muscle atrophy, muscle and joint pain, intolerance to cold, and difficulties sleeping, swallowing or breathing.

ID

http://www.orpha.net/ORDO/Orphanet_2942

alternative_term

Postpoliomyelitic syndrome

Postpoliomyelitis sequelae

Postpolio syndrome

Postpolio sequelae

definition

Postpoliomyelitis syndrome (PPS) is a neurologic disorder characterized by the development of new neuromuscular symptoms such as progressive muscular weakness or abnormal muscle fatigability occurring in survivors of the acute paralytic form of poliomyelitis (see this term), 15-40 years after recovery from the disease, and that is unexplained by other medical causes. Other manifestations that can occur gradually include generalized fatigue, muscle atrophy, muscle and joint pain, intolerance to cold, and difficulties sleeping, swallowing or breathing.

definition_citation

Orphanet

expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2942

has_age_of_onset

Adolescent

Adult

Elderly

has_inheritance

Not applicable

hasDbXref

UMLS:C0080040

ICD-11:8B62

MeSH:D016262

ICD-10:G14

label

Postpoliomyelitis syndrome

notation

ORPHA:2942

part_of

http://www.orpha.net/ORDO/Orphanet_98506

prefixIRI

ORDO:Orphanet_2942

prefLabel

Postpoliomyelitis syndrome

present_in

Worldwide AND has_point_prevalence_range : Unknown

treeView

http://www.orpha.net/ORDO/Orphanet_98506

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.ebi.ac.uk/efo/EFO_0007454 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0017416 MONDO LOOM
http://purl.obolibrary.org/obo/DOID_4952 DOID LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#15282 OCHV LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_4952 NATPRO LOOM
http://id.nlm.nih.gov/mesh/D016262 MDM LOOM
http://www.phoc.org.cn/pmo/class/PMO_00039674 PMAPP-PMO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C05.651.534.750 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.668.491.175.750 RH-MESH LOOM
http://purl.obolibrary.org/obo/OMIT_0016798 OMIT LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.574.827 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.668.864.500 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C02.782.687.359.764.650 RH-MESH LOOM
http://purl.bioontology.org/ontology/SNMI/DE-35015 SNMI LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/31097004 SNOMEDCT LOOM
http://purl.jp/bio/4/id/200906006563081125 IOBC LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.228.854.641.650 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.228.228.210.650.800 RH-MESH LOOM
http://purl.bioontology.org/ontology/MESH/D016262 MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D016262 RH-MESH LOOM
http://purl.obolibrary.org/obo/DOID_4952 DTO LOOM
http://purl.obolibrary.org/obo/DOID_4952 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_4952 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_4952 FNS-H LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.668.550.500 RH-MESH LOOM
http://purl.obolibrary.org/obo/MONDO_0017416 DOVES LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C02.182.600.700.800 RH-MESH LOOM
http://www.gamuts.net/entity#post_polio_syndrome GAMUTS REST