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 paranasal sinus morphology (HP:0000245)

Grandparent Node:
Increased inflammatory response (HP:0012649)

Parent Node:
Sinusitis (HP:0000246)

..Starting node
..Acute sinusitis (HP:0000255)

Term ID:

255

Name:

Acute sinusitis

Synonym:

Definition:

An acute form of sinusitis.

Comments:

Reference:

HP:0000255

Genes and Diseases:

Child Nodes:

Sister Nodes:

Chronic sinusitis (HP:0011109)

Recurrent sinusitis (HP:0011108)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0000255	HP:0000255	Acute sinusitis	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.