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 course (HP:0031797)

Parent Node:
Temporal pattern (HP:0011008)

..Starting node
..Diurnal (HP:0025302)

Term ID:

25302

Name:

Diurnal

Synonym:

Definition:

Applies to a sign, symptom, or other abnormality that occurs in or is exacerbated in the day time.

Comments:

Reference:

HP:0025302

Genes and Diseases:

Child Nodes:

Sister Nodes:

Acute (HP:0011009)

Chronic (HP:0011010)

Insidious onset (HP:0003587)

Migratory (HP:0025279)

Nocturnal (HP:0025301)

Prolonged (HP:0025297)

Recurrent (HP:0031796)

Subacute (HP:0011011)

Transient (HP:0025153)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025302	HP:0025302	Diurnal	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.