Human Phenotype Ontology 
Grandparent Node:
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Abnormal eye physiology (HP:0012373)help
Parent Node:
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Abnormality of eye movement (HP:0000496)help
..Starting node
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Abnormality of ocular abduction (HP:0011347)help
Term ID: 11347
Name: Abnormality of ocular abduction
Synonym:
Definition: An abnormality involving the movement of the eye outwards.
Comments:
Reference: HP:0011347
Genes and Diseases:
 
       Child Nodes:
........expandGlobe retraction and deviation on abduction (HP:0000497) help
........expandImpaired ocular abduction (HP:0000634) help

 Sister Nodes: 
..expandAbnormal conjugate eye movement (HP:0000549) help
..expandAbnormal involuntary eye movements (HP:0012547) help
..expandAbnormal ocular alignment (HP:0500073) help
..expandAbnormal saccadic eye movements (HP:0000570) help
..expandAbnormal visual fixation (HP:0025404) help
..expandAbnormality of ocular smooth pursuit (HP:0000617) help
..expandCompensatory head posture (HP:0031705) help
..expandImpaired ocular adduction (HP:0000542) help
..expandLimited extraocular movements (HP:0007941) help
..expandMarcus Gunn jaw winking synkinesis (HP:0025186) help
..expandOculomotor apraxia (HP:0000657) help
..expandOphthalmoparesis (HP:0000597) help
..expandVisual gaze preference (HP:0025518) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0011347HP:0011347Abnormality of ocular abduction0GRM1 CL E G H2911324262ORPHA1201774593604473
HP:0011347HP:0011347Abnormality of ocular abduction1GRM1 CL E G H2911324262ORPHA1201774593604473
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (4) :GRM1 MAFB MYMK SALL4

Diseases (4) :324262 617041 1358 607323
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.