Human Phenotype Ontology 
Grandparent Node:
Abnormal conjugate eye movement (HP:0000549)help
Parent Node:
Strabismus (HP:0000486)help
..Starting node
Hypodeviation (HP:0025588)help
Term ID: 25588
Name: Hypodeviation
Definition: A type of strabismus in which the visual axis of one eye is lower than that of the other.
Reference: HP:0025588
Genes and Diseases:
       Child Nodes:
........expandHypotropia (HP:0025584) help
................... HP:0500078 Alternating hypotropia
........expandHypophoria (HP:0031725) help
................... HP:0500079 Alternating hypophoria

 Sister Nodes: 
..expandConcomitant strabismus (HP:0025069) help
..expandCyclodeviation (HP:0025589) help
..expandEsodeviation (HP:0020045) help
..expandExodeviation (HP:0020049) help
..expandHyperdeviation (HP:0025587) 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:0025588HP:0025588Hypodeviation0 CL E G H
HP:0025588HP:0031725Hypophoria1 CL E G H
HP:0025588HP:0025584Hypotropia1 CL E G H
HP:0025588HP:0500079Alternating hypophoria2 CL E G H
HP:0025588HP:0500078Alternating hypotropia2 CL E G H

Genes (2) :MYF5 PHOX2A

Diseases (2) :618155 602078

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