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 coronary artery morphology (HP:0006704)

Parent Node:
Abnormal coronary artery origin (HP:0011636)

..Starting node
..Anomalous origin of the circumflex artery from the right sinus of Valsalva (HP:0025505)

Term ID:

25505

Name:

Anomalous origin of the circumflex artery from the right sinus of Valsalva

Synonym:

Definition:

The circumflex coronary artery originates from the right aortic sinus of Valsalva.

Comments:

Reference:

HP:0025505

Genes and Diseases:

Child Nodes:

........

Anomalous origin of the left circumflex artery from the right coronary artery (HP:0031537)

Sister Nodes:

Absent left main coronary artery (HP:0031639)

Anomalous coronary artery arising from the opposite sinus (HP:0025503)

Anomalous origin of coronary artery from the pulmonary artery (HP:0011637)

Coronary ostial atresia (HP:0031626)

Separate origin of the left anterior descending and left circumflex artery (HP:0031536)

Single coronary artery origin (HP:0011640)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025505	HP:0025505	Anomalous origin of the circumflex artery from the right sinus of Valsalva	0	CL E G H
HP:0025505	HP:0031537	Anomalous origin of the left circumflex artery from the right coronary artery	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.