Human Phenotype Ontology 
Grandparent Node:
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Abnormality of eye movement (HP:0000496)help
Parent Node:
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Abnormality of ocular abduction (HP:0011347)help
..Starting node
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Impaired ocular abduction (HP:0000634)help
Term ID: 634
Name: Impaired ocular abduction
Synonym:
Definition: An impaired ability of the eye to move in the outward direction (towards the side of the head).
Comments:
Reference: HP:0000634
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandGlobe retraction and deviation on abduction (HP:0000497) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0000634HP:0000634Impaired ocular abduction0MAFB CL E G H9935617041Duane retraction syndrome 3 with or without deafness617041C4310752OMIM11056408608968
HP:0000634HP:0000634Impaired ocular abduction0MAFB CL E G H9935617041Duane retraction syndrome 3 with or without deafness617041C4310752OMIM11126408608968
HP:0000634HP:0000634Impaired ocular abduction0MYMK CL E G H3898271358ORPHA17733778615345
HP:0000634HP:0000634Impaired ocular abduction0SALL4 CL E G H57167607323Duane-radial ray syndrome607323C1623209OMIM119815924607343
HP:0000634HP:0000634Impaired ocular abduction0SALL4 CL E G H57167607323Duane-radial ray syndrome607323C1623209OMIM117815924607343
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (3) :MAFB MYMK SALL4

Diseases (3) :617041 1358 607323
 

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