Human Phenotype Ontology 
Grandparent Node:
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Exodeviation (HP:0020049)help
Parent Node:
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Exotropia (HP:0000577)help
..Starting node
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Sensory exotropia (HP:0031721)help
Term ID: 31721
Name: Sensory exotropia
Synonym: Secondary exotropia
Definition: A type of divergent strabismus (exotropia) that develops in a poorly seeing eye.
Comments:
Reference: HP:0031721
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAlternating exotropia (HP:0031717) help
..expandConsecutive exotropia (HP:0031718) help
..expandConstant exotropia (HP:0031713) help
..expandCyclic exotropia (HP:0031716) help
..expandDistance exotropia (HP:0031714) help
..expandNear exotropia (HP:0031715) help
..expandobsolete Congenital exotropia (HP:0008033) 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:0031721HP:0031721Sensory exotropia0KIF21A CL E G H5560519349OMIM:135700Fibrosis of extraocular muscles, congenital, 1.93


Genes (1) :KIF21A

Diseases (1) :OMIM:135700
 

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