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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Impaired ocular adduction (HP:0000542)help
Term ID: 542
Name: Impaired ocular adduction
Synonym:
Definition: Reduced ability to move the eye in the direction of the nose.
Comments:
Reference: HP:0000542
Genes and Diseases:
 
       Child Nodes:

 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 abduction (HP:0011347) help
..expandAbnormality of ocular smooth pursuit (HP:0000617) help
..expandCompensatory head posture (HP:0031705) 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:0000542HP:0000542Impaired ocular adduction0MAFB CL E G H9935617041Duane retraction syndrome 3 with or without deafness617041C4310752OMIM1251056408608968
HP:0000542HP:0000542Impaired ocular adduction0SALL4 CL E G H57167607323Duane-radial ray syndrome607323C1623209OMIM15717115924607343
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (2) :MAFB SALL4

Diseases (2) :617041 607323
 

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