Mondo Disease Ontology

Last uploaded: November 25, 2024
Preferred Name

primary progressive aphasia
Synonyms

primary progressive aphasia syndrome

PPA

Mesulam syndrome

Definitions

Primary progressive aphasia (PPA) is a neurodegenerative disorder, characterized by a primary dissolution of language, with relative sparing of other mental faculties for at least the first 2 years of illness. PPA is recognized as the language variant in the frontotemporal dementia (FTD) spectrum of disorders. PPA can be classified into 3 subtypes based on specific speech and language features: semantic dementia (SD), progressive non-fluent aphasia (PNFA) and logopenic progressive aphasia (lv-PPA).

ID

http://purl.obolibrary.org/obo/MONDO_0019806

database_cross_reference

MESH:D018888

EFO:0009053

Orphanet:95432

DOID:0081388

GARD:8541

MEDGEN:79466

NCIT:C85024

UMLS:C0282513

definition

Primary progressive aphasia (PPA) is a neurodegenerative disorder, characterized by a primary dissolution of language, with relative sparing of other mental faculties for at least the first 2 years of illness. PPA is recognized as the language variant in the frontotemporal dementia (FTD) spectrum of disorders. PPA can be classified into 3 subtypes based on specific speech and language features: semantic dementia (SD), progressive non-fluent aphasia (PNFA) and logopenic progressive aphasia (lv-PPA).

has_exact_synonym

PPA

Mesulam syndrome

has_related_synonym

primary progressive aphasia syndrome

IAO_0000233

https://github.com/monarch-initiative/mondo/issues/5507

id

MONDO:0019806

in_subset

http://purl.obolibrary.org/obo/mondo/mondo-simple#otar

http://purl.obolibrary.org/obo/mondo/mondo-simple#ordo_group_of_disorders

http://purl.obolibrary.org/obo/mondo/mondo-simple#rare

http://purl.obolibrary.org/obo/mondo/mondo-simple#disease_grouping

http://purl.obolibrary.org/obo/mondo/mondo-simple#gard_rare

label

primary progressive aphasia

notation

MONDO:0019806

prefLabel

primary progressive aphasia

skos_exactMatch

http://identifiers.org/medgen/79466

http://purl.obolibrary.org/obo/Orphanet_95432

http://purl.obolibrary.org/obo/EFO_0009053

http://purl.obolibrary.org/obo/DOID_0081388

http://linkedlifedata.com/resource/umls/id/C0282513

http://purl.obolibrary.org/obo/NCIT_C85024

http://identifiers.org/mesh/D018888

treeView

http://purl.obolibrary.org/obo/MONDO_0005559

subClassOf

http://purl.obolibrary.org/obo/MONDO_0005559

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