The Biomarker Ontology

Last uploaded: June 3, 2024
Preferred Name

pulmonary arterial hypertension

Synonyms

Ayerza's Syndrome

Hypertension, Pulmonary

pulmonary hypertension

Pulmonary hypertension, NOS

pulmonary hypertension, primary, 1

Syndrome, Ayerza-Arrilaga

Ayerzas Syndrome

Syndrome, Ayerza

HYPERTENSION PULM

pulmonary arterial hypertension

PHT - Pulmonary hypertension

PULM HYPERTENSION

Ayerza-Arrilaga Syndrome

pulmonary hypertension (disorder)

Ayerza Arrilaga Syndrome

Ayerza Syndrome

PAH

PPH1

idiopathic pulmonary hypertension

PPH

PAH with overt features of venous/capillaries involvement

PVOD/PCH

Definitions

A syndrome with pathological changes in the pulmonary arteries and impaired PULMONARY CIRCULATION that can be the result of PULMONARY HYPERTENSION. Ayerza syndrome is characterized by slowly developing ASTHMA; BRONCHITIS; DYSPNEA; and CYANOSIS in association with POLYCYTHEMIA. Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease). Increased VASCULAR RESISTANCE in the PULMONARY CIRCULATION, usually secondary to HEART DISEASES or LUNG DISEASES.

ID

http://www.ebi.ac.uk/efo/EFO_0001361

closeMatch

http://identifiers.org/meddra/10064911

database cross reference

MedDRA:10064911

SCTID:11399002

Orphanet:182090

SNOMEDCT:70995007

MONDO:0015924

MESH:D000081029

OMIM:615371

UMLS:C2973725

MeSH:D006976

DOID:6432

GARD:7501

NCIt:C3120

NORD:1634

exactMatch

http://identifiers.org/mesh/D000081029

http://identifiers.org/snomedct/11399002

http://purl.obolibrary.org/obo/Orphanet_182090

http://linkedlifedata.com/resource/umls/id/C2973725

gwas_trait

true

has_narrow_synonym

PAH with overt features of venous/capillaries involvement

PVOD/PCH

has_related_synonym

idiopathic pulmonary hypertension

PPH

hasExactSynonym

Ayerza's Syndrome

Hypertension, Pulmonary

pulmonary hypertension

Pulmonary hypertension, NOS

pulmonary hypertension, primary, 1

Syndrome, Ayerza-Arrilaga

Ayerzas Syndrome

Syndrome, Ayerza

HYPERTENSION PULM

pulmonary arterial hypertension

PHT - Pulmonary hypertension

PULM HYPERTENSION

Ayerza-Arrilaga Syndrome

pulmonary hypertension (disorder)

Ayerza Arrilaga Syndrome

Ayerza Syndrome

PAH

PPH1

id

EFO:0001361

imported from

http://www.ebi.ac.uk/efo/efo.owl

in subset

http://purl.oboInOwllibrary.org/oboInOwl/mondo#rare

http://purl.oboInOwllibrary.org/oboInOwl/mondo#gard_rare

http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_group_of_disorders

http://purl.oboInOwllibrary.org/oboInOwl/mondo#nord_rare

http://purl.oboInOwllibrary.org/oboInOwl/mondo#disease_grouping

http://purl.oboInOwllibrary.org/oboInOwl/mondo#orphanet_rare

label

pulmonary arterial hypertension

notation

EFO:0001361

prefLabel

pulmonary arterial hypertension

term editor

James Malone

term tracker item

https://github.com/monarch-initiative/mondo/issues/5537

https://github.com/monarch-initiative/mondo/issues/5781

textual definition

A syndrome with pathological changes in the pulmonary arteries and impaired PULMONARY CIRCULATION that can be the result of PULMONARY HYPERTENSION. Ayerza syndrome is characterized by slowly developing ASTHMA; BRONCHITIS; DYSPNEA; and CYANOSIS in association with POLYCYTHEMIA.

Pulmonary arterial hypertension (PAH) is a group of diseases characterized by mean pulmonary artery pressure >20 mmHg and elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, have overt features of venous/capillary involvement (pulmonary veno-occlusive disease, PVOD/pulmonary capillary hemangiomatosis, PCH), induced by drug or toxin (drug-or toxin-induced PAH), or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease).

Increased VASCULAR RESISTANCE in the PULMONARY CIRCULATION, usually secondary to HEART DISEASES or LUNG DISEASES.

subClassOf

http://purl.obolibrary.org/obo/DOID_10763

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Delete Mapping To Ontology Source
http://www.ebi.ac.uk/efo/EFO_0001361 EFO SAME_URI
http://purl.obolibrary.org/obo/HP_0002092 MAXO LOOM
http://purl.obolibrary.org/obo/MONDO_0015924 MONDO LOOM
http://purl.obolibrary.org/obo/HP_0002092 OBA LOOM
http://nanbyodata.jp/ontology/NANDO_2200298 NANDO LOOM
http://nanbyodata.jp/ontology/NANDO_1200425 NANDO LOOM
http://nanbyodata.jp/ontology/NANDO_2100103 NANDO LOOM
http://www.ebi.ac.uk/efo/EFO_0001361 EFO LOOM
http://purl.obolibrary.org/obo/HP_0002092 HP LOOM
http://purl.obolibrary.org/obo/HP_0002092 OBA LOOM
http://www.limics.org/hrdo/rdfns#pat_id_18210 HRDO LOOM
http://purl.obolibrary.org/obo/NCIT_C157552 BERO LOOM
http://purl.obolibrary.org/obo/MONDO_0015924 DOVES LOOM
http://purl.obolibrary.org/obo/MONDO_0015924 KTAO LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C2973725 MEDLINEPLUS LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU037923 OMIM LOOM
http://www.phoc.org.cn/pmo/class/PMO_00011611 PMAPP-PMO LOOM
http://www.orpha.net/ORDO/Orphanet_182090 ORDO LOOM
http://purl.bioontology.org/ontology/MEDDRA/10064911 MEDDRA LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C536282 RH-MESH LOOM
http://id.nlm.nih.gov/mesh/D000081029 MDM LOOM
http://purl.obolibrary.org/obo/HP_0002092 HP LOOM
http://purl.obolibrary.org/obo/HP_0002092 UPHENO LOOM
http://purl.jp/bio/4/id/201206045811803680 IOBC LOOM
http://purl.jp/bio/4/id/200906048557252117 IOBC LOOM
http://bmi.utah.edu/ontologies/hfontology/C2973725 HFO LOOM
http://purl.bioontology.org/ontology/MESH/D000081029 MESH LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/11399002 SNOMEDCT LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C157552 NCIT LOOM
http://www.gamuts.net/entity#pulmonary_arterial_hypertension GAMUTS LOOM