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:
Atrioventricular block (HP:0001678)

Parent Node:
Third degree atrioventricular block (HP:0001709)

..Starting node
..Complete heart block with narrow QRS complexes (HP:0005178)

Term ID:

5178

Name:

Complete heart block with narrow QRS complexes

Synonym:

Definition:

A type of third degree heart block in which the escape rhythm arises at the atrioventricular node, which produces a narrow QRS complex.

Comments:

Reference:

HP:0005178

Genes and Diseases:

Child Nodes:

Sister Nodes:

Complete heart block with broad QRS complexes (HP:0005170)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0005178	HP:0005178	Complete heart block with narrow QRS complexes	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.