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 entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0000634HP:0000634Impaired ocular abduction0MAFB CL E G H99356408OMIM:617041Duane retraction syndrome 3 with or without deafness.63
HP:0000634HP:0000634Impaired ocular abduction0MYMK CL E G H38982733778ORPHA:1358Carey-Fineman-Ziter syndromeHP:0040281 - Very frequent5
HP:0000634HP:0000634Impaired ocular abduction0MYMX CL E G H10192972652391ORPHA:1358Carey-Fineman-Ziter syndromeHP:0040281 - Very frequent
HP:0000634HP:0000634Impaired ocular abduction0ROBO3 CL E G H6422113433OMIM:607313Gaze palsy, familial horizontal, with progressive scoliosis, 190
HP:0000634HP:0000634Impaired ocular abduction0SALL4 CL E G H5716715924OMIM:607323Duane-Radial ray syndrome.86


Genes (5) :MAFB MYMK MYMX ROBO3 SALL4

Diseases (4) :OMIM:617041 ORPHA:1358 OMIM:607313 OMIM:607323
 

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