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 systemic arterial morphology (HP:0011004)

Grandparent Node:
Vascular tortuosity (HP:0004948)

Parent Node:
Arterial tortuosity (HP:0005116)

..Starting node
..Temporal artery tortuosity (HP:0030165)

Term ID:

30165

Name:

Temporal artery tortuosity

Synonym:

Definition:

The presence of an increased number of twists and turns of the temporal artery.

Comments:

Reference:

HP:0030165

Genes and Diseases:

Child Nodes:

Sister Nodes:

Carotid artery tortuosity (HP:0005302)

Generalized arterial tortuosity (HP:0004955)

Retinal arterial tortuosity (HP:0000631)

Tortuous cerebral arteries (HP:0004938)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030165	HP:0030165	Temporal artery tortuosity	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.