Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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:
Clinical modifier (HP:0012823)

Parent Node:
Pain characteristic (HP:0025280)

..Starting node
..Dull (HP:0025282)

Term ID:

25282

Name:

Dull

Synonym:

Dull pain

Definition:

Applied to pain that is dull, i.e., not severe but that continues over a long period of time.

Comments:

Reference:

HP:0025282

Genes and Diseases:

Child Nodes:

Sister Nodes:

Sharp (HP:0025281)

Sleep-interrupting (HP:0025284)

Tender (HP:0025283)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025282	HP:0025282	Dull	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.