Human Phenotype Ontology 
Grandparent Node:
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Abnormal conjugate eye movement (HP:0000549)help
Parent Node:
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Strabismus (HP:0000486)help
..Starting node
..expand
Hyperdeviation (HP:0025587)help
Term ID: 25587
Name: Hyperdeviation
Synonym:
Definition: A type of strabismus in which the visual axis of one eye is higher than that of the other.
Comments:
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 entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025587HP:0025587Hyperdeviation0FBN1 CL E G H22003603OMIM:154700Marfan syndrome1361
HP:0025587HP:0025587Hyperdeviation0PHOX2A CL E G H401691OMIM:602078Fibrosis of extraocular muscles, congenital, 26
HP:0025587HP:0025587Hyperdeviation0SALL2 CL E G H629710526OMIM:216820COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE1
HP:0025587HP:0025585Hyperphoria1 CL E G H
HP:0025587HP:0025586Hypertropia1FBN1 CL E G H22003603OMIM:154700Marfan syndrome1361
HP:0025587HP:0025586Hypertropia1PHOX2A CL E G H401691OMIM:602078Fibrosis of extraocular muscles, congenital, 2.6
HP:0025587HP:0025586Hypertropia1SALL2 CL E G H629710526OMIM:216820COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE1
HP:0025587HP:0500077Alternating hyperphoria2 CL E G H
HP:0025587HP:0500076Alternating hypertropia2 CL E G H


Genes (3) :FBN1 PHOX2A SALL2

Diseases (3) :OMIM:154700 OMIM:602078 OMIM:216820
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.