Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Pneumonia (HP:0002090)

Parent Node:
Aspiration pneumonia (HP:0011951)

..Starting node
..Acute aspiration pneumonia (HP:0011952)

Term ID:

11952

Name:

Acute aspiration pneumonia

Synonym:

Definition:

An acute episode of pneumonia due to the aspiration (breathing in) of food, liquid, or gastric contents into the upper respiratory tract.

Comments:

Reference:

HP:0011952

Genes and Diseases:

Child Nodes:

Sister Nodes:

Recurrent aspiration pneumonia (HP:0002100)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011952	HP:0011952	Acute aspiration pneumonia	0	CL E G H

Genes (0) :

Diseases (0) :

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