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:
Supraventricular arrhythmia (HP:0005115)

Parent Node:
Atrial arrhythmia (HP:0001692)

..Starting node
..Automatic atrial tachycardia (HP:0011700)

Term ID:

11700

Name:

Automatic atrial tachycardia

Synonym:

Definition:

Chronic supraventricular tachycardia predominantly seen in childhood.

Comments:

Reference:

HP:0011700

Genes and Diseases:

Child Nodes:

Sister Nodes:

Atrial fibrillation (HP:0005110)

Atrial flutter (HP:0004749)

Atrial reentry tachycardia (HP:0011699)

Chaotic multifocal atrial tachycardia (HP:0011725)

Multifocal atrial tachycardia (HP:0011701)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011700	HP:0011700	Automatic atrial tachycardia	0	CITED2 CL E G H	10370	1987	ORPHA:99105	Atrial septal defect, sinus venosus type	HP:0040283 - Occasional	5

Genes (1) :CITED2

Diseases (1) :ORPHA:99105

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