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:
Clinical modifier (HP:0012823)

Parent Node:
Pain characteristic (HP:0025280)

..Starting node
..Sleep-interrupting (HP:0025284)

Term ID:

25284

Name:

Sleep-interrupting

Synonym:

Definition:

Applied to pain that wakes the affecting individual from sleep.

Comments:

Reference:

HP:0025284

Genes and Diseases:

Child Nodes:

Sister Nodes:

Dull (HP:0025282)

Sharp (HP:0025281)

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:0025284	HP:0025284	Sleep-interrupting	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.