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

..Starting node
..Prolonged P wave (HP:0034308)

Term ID:

34308

Name:

Prolonged P wave

Synonym:

Definition:

Abnormal increased in the duration of the P wave, which is a marker of delayed inter-atrial conduction.

Comments:

Reference:

HP:0034308

Genes and Diseases:

Child Nodes:

Sister Nodes:

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:0034308	HP:0034308	Prolonged P wave	0	GJA5 CL E G H	2702	4279	OMIM:614049	Atrial fibrillation, familial, 11	39
HP:0034308	HP:0034308	Prolonged P wave	0	SCN3B CL E G H	55800	20665	OMIM:613120	Brugada syndrome 7	122

Genes (2) :GJA5 SCN3B

Diseases (2) :OMIM:614049 OMIM:613120

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