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:
Ventricular arrhythmia (HP:0004308)

Parent Node:
Ventricular preexcitation (HP:0004309)

..Starting node
..Ventricular preexcitation with multiple accessory pathways (HP:0006684)

Term ID:

6684

Name:

Ventricular preexcitation with multiple accessory pathways

Synonym:

Definition:

A form of ventricular preexcitation due to the presence of multiple accessory pathways for cardiac conduction.

Comments:

Reference:

HP:0006684

Genes and Diseases:

Child Nodes:

Sister Nodes:

Wolff-Parkinson-White syndrome (HP:0001716)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006684	HP:0006684	Ventricular preexcitation with multiple accessory pathways	0	PRKAG2 CL E G H	51422	9386	OMIM:194200	WOLFF-PARKINSON-WHITE SYNDROME	235

Genes (1) :PRKAG2

Diseases (1) :OMIM:194200

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