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:
Recurrent infections (HP:0002719)

Grandparent Node:
Respiratory tract infection (HP:0011947)

Parent Node:
Recurrent respiratory infections (HP:0002205)

..Starting node
..Respiratory infections in early life (HP:0004880)

Term ID:

4880

Name:

Respiratory infections in early life

Synonym:

Definition:

Increased susceptibility to respiratory infections in early life, as manifested by recurrent episodes of respiratory infections.

Comments:

Reference:

HP:0004880

Genes and Diseases:

Child Nodes:

Sister Nodes:

Recurrent bronchopulmonary infections (HP:0006538)

Recurrent infections due to aspiration (HP:0004891)

Recurrent lower respiratory tract infections (HP:0002783)

Recurrent sinopulmonary infections (HP:0005425)

Recurrent streptococcus pneumoniae infections (HP:0005366)

Recurrent upper respiratory tract infections (HP:0002788)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0004880	HP:0004880	Respiratory infections in early life	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.