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:
Carotid artery dissection (HP:0012158)

Parent Node:
Arterial dissection (HP:0005294)

Parent Node:
Internal carotid artery dissection (HP:0012159)

..Starting node
..Extracranial internal carotid artery dissection (HP:0004945)

Term ID:

4945

Name:

Extracranial internal carotid artery dissection

Synonym:

Definition:

A separation (dissection) of the layers of the extracranial portion of the internal carotid artery wall.

Comments:

Reference:

HP:0004945

Genes and Diseases:

Child Nodes:

Sister Nodes:

Intracranial internal carotid artery dissection (HP:0012160)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0004945	HP:0004945	Extracranial internal carotid artery dissection	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.