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 anatomic location of the heart (HP:0004307)

Parent Node:
Abnormal direction of ventricular apex (HP:0011600)

..Starting node
..Midline direction of ventricular apex (HP:0011602)

Term ID:

11602

Name:

Midline direction of ventricular apex

Synonym:

Definition:

Abnormal plane of direction of the heart from the base to the apex in the midline. Left sided is normal.

Comments:

Reference:

HP:0011602

Genes and Diseases:

Child Nodes:

Sister Nodes:

Rightward direction of ventricular apex (HP:0011601)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011602	HP:0011602	Midline direction of ventricular apex	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.