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 ventriculoarterial connection (HP:0011563)

Grandparent Node:
Congenital malformation of the great arteries (HP:0011603)

Parent Node:
Transposition of the great arteries (HP:0001669)

..Starting node
..Levotransposition of the great arteries (HP:0031349)

Term ID:

31349

Name:

Levotransposition of the great arteries

Synonym:

L-TGA

Definition:

A type of transposition of the great arteries (TGA) in which aorta is in front of and primarily to the left of the pulmonary artery.

Comments:

Reference:

HP:0031349

Genes and Diseases:

Child Nodes:

Sister Nodes:

Dextrotransposition of the great arteries (HP:0031348)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031349	HP:0031349	Levotransposition of the great arteries	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.