Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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 aortic arch morphology (HP:0012303)

Grandparent Node:
Coarctation of aorta (HP:0001680)

Parent Node:
Coarctation of the descending aortic arch (HP:0012305)

..Starting node
..Juxtaductal coarctation of the aorta (HP:0011646)

Term ID:

11646

Name:

Juxtaductal coarctation of the aorta

Synonym:

Definition:

Narrowing or constriction of the aorta localized at the insertion of the ductus arteriosus, i.e., to the juxtaductal region of aortic arch.

Comments:

Reference:

HP:0011646

Genes and Diseases:

Child Nodes:

Sister Nodes:

Postductal coarctation of the aorta (HP:0011647)

Preductal coarctation of the aorta (HP:0005151)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011646	HP:0011646	Juxtaductal coarctation of the aorta	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.