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:
Aggravated by (HP:0025285)

..Starting node
..Exacerbated by head trauma (HP:0025315)

Term ID:

25315

Name:

Exacerbated by head trauma

Synonym:

Definition:

Applies to a sign or symptom that is worsened, aggravated, or exacerbated by head trauma.

Comments:

Reference:

HP:0025315

Genes and Diseases:

Child Nodes:

Sister Nodes:

Aggravated by activity (HP:0025286)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025315	HP:0025315	Exacerbated by head trauma	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.