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:
Cardiomyopathy (HP:0001638)

Parent Node:
Noncompaction cardiomyopathy (HP:0012817)

..Starting node
..Right ventricular noncompaction cardiomyopathy (HP:0012816)

Term ID:

12816

Name:

Right ventricular noncompaction cardiomyopathy

Synonym:

Definition:

A predominantly right ventricular variant of isolated noncompaction cardiomyopathy.

Comments:

Reference:

HP:0012816

Genes and Diseases:

Child Nodes:

Sister Nodes:

Biventricular noncompaction cardiomyopathy (HP:0012818)

Left ventricular noncompaction cardiomyopathy (HP:0011664)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012816	HP:0012816	Right ventricular noncompaction cardiomyopathy	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.