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:
Abnormal respiratory system physiology (HP:0002795)

Parent Node:
Cough (HP:0012735)

..Starting node
..Nonproductive cough (HP:0031246)

Term ID:

31246

Name:

Nonproductive cough

Synonym:

Dry cough; Dry coughing

Definition:

A cough that does not produce phlegm or mucus.

Comments:

Reference:

HP:0031246

Genes and Diseases:

Child Nodes:

Sister Nodes:

Productive cough (HP:0031245)

Whooping cough (HP:0031247)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031246	HP:0031246	Nonproductive cough	0	SLC34A2 CL E G H	10568	11020	ORPHA:60025	Pulmonary alveolar microlithiasis	HP:0040282 - Frequent	7

Genes (1) :SLC34A2

Diseases (1) :ORPHA:60025

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