Human Phenotype Ontology 
Grandparent Node:
Abnormality of eye movement (HP:0000496)help
Parent Node:
Compensatory head posture (HP:0031705)help
..Starting node
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.
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 entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0001477HP:0001477Compensatory chin elevation0COL25A1 CL E G H8457018603ORPHA:91411Congenital ptosis3
HP:0001477HP:0001477Compensatory chin elevation0KIF21A CL E G H5560519349OMIM:135700Fibrosis of extraocular muscles, congenital, 1.93
HP:0001477HP:0001477Compensatory chin elevation0TUBB3 CL E G H1038120772OMIM:600638Fibrosis of extraocular muscles, congenital, 3A, with or without extraocularinvolvement.64
HP:0001477HP:0001477Compensatory chin elevation0ZFHX4 CL E G H7977630939ORPHA:91411Congenital ptosis

Genes (4) :COL25A1 KIF21A TUBB3 ZFHX4

Diseases (3) :ORPHA:91411 OMIM:135700 OMIM:600638

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