Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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 cardiac ventricle morphology (HP:0001713)

Parent Node:
Abnormal right ventricle morphology (HP:0001707)

..Starting node
..Anomalous muscle bundle of the right ventricle (HP:0030740)

Term ID:

30740

Name:

Anomalous muscle bundle of the right ventricle

Synonym:

Right ventricular anomalous muscle bundle

Definition:

An accessory (not normally present) muscle bundle in the right ventricle which obstructs the right ventricular outflow tract.

Comments:

Reference:

HP:0030740

Genes and Diseases:

Child Nodes:

Sister Nodes:

Cor pulmonale (HP:0001648)

Hypoplasia of right ventricle (HP:0004762)

Right ventricular dilatation (HP:0005133)

Right ventricular hypertrophy (HP:0001667)

Right ventricular outlet tract obstruction (HP:0001705)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030740	HP:0030740	Anomalous muscle bundle of the right ventricle	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.