Human Phenotype Ontology 
Grandparent Node:
expandAbnormal respiratory system physiology (HP:0002795)help
Grandparent Node:
expandImmunologic hypersensitivity (HP:0100326)help
Parent Node:
expandAsthma (HP:0002099)help
..Starting node
..expandAspirin-induced asthma (HP:0012042)help
Term ID: 12042
Name: Aspirin-induced asthma
Synonym: Aspirin-induced asthma
Definition: A type of asthma in which aspirin and other nonsteroidal anti-inflammatory drugs (NSAIDs) that inhibit cyclooxygen-ase 1 (COX-1) exacerbate bronchoconstriction.
Comments:
Reference: HP:0012042
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandExercise-induced asthma (HP:0012652) help
..expandStatus asthmaticus (HP:0012653) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012042HP:0012042Aspirin-induced asthma0PTGER2 CL E G H57329594OMIM:208550Asthma, nasal polyps, and aspirin intolerance.1
HP:0012042HP:0012042Aspirin-induced asthma0TBX21 CL E G H3000911599OMIM:208550Asthma, nasal polyps, and aspirin intolerance.1


Genes (2) :PTGER2 TBX21

Diseases (1) :OMIM:208550
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.