Human Phenotype Ontology 
Grandparent Node:
expandAbnormal eye physiology (HP:0012373)help
Parent Node:
expandAbnormality of eye movement (HP:0000496)help
..Starting node
..expandAbnormal ocular alignment (HP:0500073)help
Term ID: 500073
Name: Abnormal ocular alignment
Synonym:
Definition: Any deviation from the normal ocular alignment.
Comments:
Reference: HP:0500073
Genes and Diseases:
 
       Child Nodes:
........expandDissociated vertical deviation (HP:0500074) help
........expandDissociated horizontal deviation (HP:0500075) help

 Sister Nodes: 
..expandAbnormal conjugate eye movement (HP:0000549) help
..expandAbnormal involuntary eye movements (HP:0012547) 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
..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 entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0500073HP:0500073Abnormal ocular alignment0 CL E G H
HP:0500073HP:0500075Dissociated horizontal deviation1 CL E G H
HP:0500073HP:0500074Dissociated vertical deviation1 CL E G H


Genes (0) :

Diseases (0) :
 

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