Human Phenotype Ontology 
Grandparent Node:
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Strabismus (HP:0000486)help
Parent Node:
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Exodeviation (HP:0020049)help
..Starting node
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Exophoria (HP:0025313)help
Term ID: 25313
Name: Exophoria
Synonym:
Definition: A form of strabismus with one or both eyes deviated outward to a milder degree than with exotropia.
Comments:
Reference: HP:0025313
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandExotropia (HP:0000577) 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:0025313HP:0025313Exophoria0AFF4 CL E G H2712517869ORPHA:444077Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndromeHP:0040283 - Occasional6
HP:0025313HP:0025313Exophoria0GJA5 CL E G H27024279OMIM:612474Chromosome 1q21.1 deletion syndrome, 1.35-mb39
HP:0025313HP:0025313Exophoria0GJA8 CL E G H27034281OMIM:612474Chromosome 1q21.1 deletion syndrome, 1.35-mb34
HP:0025313HP:0025313Exophoria0HACE1 CL E G H5753121033ORPHA:464282Spastic paraplegia-severe developmental delay-epilepsy syndromeHP:0040282 - Frequent10
HP:0025313HP:0025313Exophoria0TRAPPC11 CL E G H6068425751ORPHA:369840TRAPPC11-related limb-girdle muscular dystrophy R18HP:0040283 - Occasional27


Genes (5) :AFF4 GJA5 GJA8 HACE1 TRAPPC11

Diseases (4) :ORPHA:444077 OMIM:612474 ORPHA:464282 ORPHA:369840
 

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