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:
Strabismus (HP:0000486)

Parent Node:
Hyperdeviation (HP:0025587)

..Starting node
..Hyperphoria (HP:0025585)

Term ID:

25585

Name:

Hyperphoria

Synonym:

Definition:

Tendency for the visual axis of one eye to be higher than that of the other.

Comments:

Reference:

HP:0025585

Genes and Diseases:

Child Nodes:

........

Alternating hyperphoria (HP:0500077)

Sister Nodes:

Hypertropia (HP:0025586)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025585	HP:0025585	Hyperphoria	0	CL E G H
HP:0025585	HP:0500077	Alternating hyperphoria	1	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.