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
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Incomitant strabismus (HP:0025068)help
Term ID: 25068
Name: Incomitant strabismus
Synonym:
Definition: Strabismus in which the angle of deviation differs depending upon the direction of gaze or according to which eye is fixing, associated with: (i) defective movement of the eye, (ii) asymmetrical accommodative effort.
Comments:
Reference: HP:0025068
Genes and Diseases:
 
       Child Nodes:
........expandDuane anomaly (HP:0009921) help
........expandDouble elevator palsy (HP:0020041) help
........expandDouble depressor palsy (HP:0020042) help
........expandVertically incomitant strabismus (HP:0020043) help
........expandHorizontally incomitant strabismus (HP:0020044) help
........expandBrown anomaly (HP:0031622) help

 Sister Nodes: 
..expandConcomitant strabismus (HP:0025069) help
..expandCyclodeviation (HP:0025589) help
..expandEsodeviation (HP:0020045) help
..expandExodeviation (HP:0020049) help
..expandHyperdeviation (HP:0025587) help
..expandHypodeviation (HP:0025588) 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:0025068HP:0025068Incomitant strabismus0 CL E G H
HP:0025068HP:0009921Duane anomaly1 CL E G H
HP:0025068HP:0020041Double elevator palsy1 CL E G H
HP:0025068HP:0020042Double depressor palsy1 CL E G H
HP:0025068HP:0020043Vertical incomitant strabismus1 CL E G H
HP:0025068HP:0031622Brown anomaly1 CL E G H
HP:0025068HP:0020044Horizontal incomitant strabismus1 CL E G H


Genes (10) :ARX CCNQ CHN1 CREBBP CSPP1 EP300 KIAA0586 PIEZO2 SALL1 SALL4

Diseases (8) :300215 300707 604356 180849 397715 108145 107480 607323
 

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