Human Phenotype Ontology 
Grandparent Node:
Abnormal conjugate eye movement (HP:0000549)help
Parent Node:
Strabismus (HP:0000486)help
..Starting node
Hyperdeviation (HP:0025587)help
Term ID: 25587
Name: Hyperdeviation
Definition: A type of strabismus in which the visual axis of one eye is higher than that of the other.
Reference: HP:0025587
Genes and Diseases:
       Child Nodes:
........expandHyperphoria (HP:0025585) help
................... HP:0500077 Alternating hyperphoria
........expandHypertropia (HP:0025586) help
................... HP:0500076 Alternating hypetropia

 Sister Nodes: 
..expandConcomitant strabismus (HP:0025069) help
..expandCyclodeviation (HP:0025589) help
..expandEsodeviation (HP:0020045) help
..expandExodeviation (HP:0020049) help
..expandHypodeviation (HP:0025588) help
..expandIncomitant strabismus (HP:0025068) help
..expandMicrotropia (HP:0031724) help
..expandMonocular strabismus (HP:0010877) help
..expandNeurogenic strabismus (HP:0031775) help
..expandobsolete Congenital strabismus (HP:0000487) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025587HP:0025587Hyperdeviation0 CL E G H
HP:0025587HP:0025585Hyperphoria1 CL E G H
HP:0025587HP:0025586Hypertropia1 CL E G H
HP:0025587HP:0500077Alternating hyperphoria2 CL E G H
HP:0025587HP:0500076Alternating hypertropia2 CL E G H

Genes (3) :FBN1 PHOX2A SALL2

Diseases (3) :154700 602078 216820

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.