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:
Rhinitis (HP:0012384)

Parent Node:
Chronic rhinitis (HP:0002257)

..Starting node
..Chronic rhinitis due to narrow nasal airway (HP:0004499)

Term ID:

4499

Name:

Chronic rhinitis due to narrow nasal airway

Synonym:

Chronic nasal inflammation due to narrow nasal airway

Definition:

Comments:

Reference:

HP:0004499

Genes and Diseases:

Child Nodes:

Sister Nodes:

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:0004499	HP:0004499	Chronic rhinitis due to narrow nasal airway	0	TNFSF11 CL E G H	8600	11926	OMIM:259710	Osteopetrosis, autosomal recessive 2	.	44

Genes (1) :TNFSF11

Diseases (1) :OMIM:259710

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