Human Phenotype Ontology 
Grandparent Node:
expandAbnormal eye physiology (HP:0012373)help
Parent Node:
expandAbnormality of eye movement (HP:0000496)help
..Starting node
..expandCompensatory head posture (HP:0031705)help
Term ID: 31705
Name: Compensatory head posture
Synonym:
Definition: A compensatory head posture occurs when the head is deviated out of the normal primary straight head position in order to compensate for an ocular problem.
Comments:
Reference: HP:0031705
Genes and Diseases:
 
       Child Nodes:
........expandCompensatory chin elevation (HP:0001477) help
........expandCompensatory chin depression (HP:0031706) help
........expandCompensatory face turn to the right (HP:0031707) help
........expandCompensatory face turn to the left (HP:0031708) help
........expandCompensatory head tilt to the right shoulder (HP:0031709) help
........expandCompensatory head tilt to the left shoulder (HP:0031710) 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 abduction (HP:0011347) help
..expandAbnormality of ocular smooth pursuit (HP:0000617) 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:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031705HP:0031705Compensatory head posture0 CL E G H
HP:0031705HP:0031705Compensatory head posture1 CL E G H


Genes (2) :KIF21A TUBB3

Diseases (2) :135700 600638
 

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