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 EKG (HP:0003115)

Parent Node:
Abnormal QRS complex (HP:0025074)

..Starting node
..Abnormal QRS voltage (HP:0025076)

Term ID:

25076

Name:

Abnormal QRS voltage

Synonym:

Definition:

Abnormal amplitude of the QRS complex of the electrocardiogram (EKG).

Comments:

Reference:

HP:0025076

Genes and Diseases:

Child Nodes:

........

Increased QRS voltage (HP:0025075)

........

Decreased QRS voltage (HP:0025077)

........

Electrical alternans (HP:0025078)

Sister Nodes:

Prolonged QRS complex (HP:0006677)

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:0025076	HP:0025076	Abnormal QRS voltage	0	SVIL CL E G H	6840	11480	OMIM:619040	MYOFIBRILLAR MYOPATHY 10; MFM10	1
HP:0025076	HP:0025078	Electrical alternans	1	CL E G H
HP:0025076	HP:0025077	Decreased QRS voltage	1	CL E G H
HP:0025076	HP:0025075	Increased QRS voltage	1	SVIL CL E G H	6840	11480	OMIM:619040	MYOFIBRILLAR MYOPATHY 10; MFM10	1

Genes (1) :SVIL

Diseases (1) :OMIM:619040

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