Human Phenotype Ontology 
Grandparent Node:
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Abnormality of eye movement (HP:0000496)help
Parent Node:
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Compensatory head posture (HP:0031705)help
..Starting node
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Compensatory chin elevation (HP:0001477)help
Term ID: 1477
Name: Compensatory chin elevation
Synonym: Compensatory head tilt/chin elevation
Definition: A tendency to hold the chin elevated by about 20 to 30 degrees to compensate for a limitation of eye movement.
Comments:
Reference: HP:0001477
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCompensatory chin depression (HP:0031706) help
..expandCompensatory face turn to the left (HP:0031708) help
..expandCompensatory face turn to the right (HP:0031707) help
..expandCompensatory head tilt to the left shoulder (HP:0031710) help
..expandCompensatory head tilt to the right shoulder (HP:0031709) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0001477HP:0001477Compensatory chin elevation0KIF21A CL E G H55605135700Fibrosis of extraocular muscles, congenital, 1135700C1851102OMIM117519349608283
HP:0001477HP:0001477Compensatory chin elevation0TUBB3 CL E G H10381600638Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement600638C2748801OMIM120520772602661
HP:0001477HP:0001477Compensatory chin elevation0TUBB3 CL E G H10381600638Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement600638C2748801OMIM121720772602661
 
HPO disease - gene - phenotype less frequent non-typical associations:


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 August 2021 release.