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 coronary artery from the pulmonary artery (HP:0011637)

Term ID:

11637

Name:

Anomalous origin of coronary artery from the pulmonary artery

Synonym:

Definition:

A coronary artery begins (branches off from) the pulmonary artery rather than as normal from the root of the aorta.

Comments:

Reference:

HP:0011637

Genes and Diseases:

Child Nodes:

........

Anomalous origin of left coronary artery from the pulmonary artery (HP:0011638)

........

Anomalous origin of right coronary artery from the pulmonary artery (HP:0011639)

........

Anomalous origin of the left anterior descending artery from the pulmonary artery (HP:0031638)

Sister Nodes:

Absent left main coronary artery (HP:0031639)

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

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

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	Gene id entrez	HGNC ID	DiseaseId	DiseaseName
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011637	HP:0011637	Anomalous origin of coronary artery from the pulmonary artery	0	NADSYN1 CL E G H	55191	29832	OMIM:618845	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 3; VCRL3
HP:0011637	HP:0011639	Anomalous origin of right coronary artery from the pulmonary artery	1	CL E G H
HP:0011637	HP:0031638	Anomalous origin of the left anterior descending artery from the pulmonary artery	1	CL E G H
HP:0011637	HP:0011638	Anomalous origin of left coronary artery from the pulmonary artery	1	NADSYN1 CL E G H	55191	29832	OMIM:618845	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 3; VCRL3

Genes (1) :NADSYN1

Diseases (1) :OMIM:618845

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.