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:
Arterial calcification (HP:0003207)

Parent Node:
Intracranial arterial calcification (HP:0031306)

..Starting node
..Cerebral artery calcification (HP:0031309)

Term ID:

31309

Name:

Cerebral artery calcification

Synonym:

Definition:

An accumulation of calcium and phosphate in arteries with mineral deposits in the intimal or medial layer of the vessel wall in a cerebral artery.

Comments:

Reference:

HP:0031309

Genes and Diseases:

Child Nodes:

........

Middle cerebral artery calcification (HP:0031311)

Sister Nodes:

Basilar artery calcification (HP:0031310)

Calcification of the small brain vessels (HP:0002504)

Internal carotid artery calcification (HP:0031307)

Vertebral artery calcification (HP:0031308)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031309	HP:0031309	Cerebral artery calcification	0	CL E G H
HP:0031309	HP:0031311	Middle cerebral artery calcification	1	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.