Human Phenotype Ontology 
Grandparent Node:
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Strabismus (HP:0000486)help
Parent Node:
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Esodeviation (HP:0020045)help
..Starting node
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Esophoria (HP:0025312)help
Term ID: 25312
Name: Esophoria
Synonym:
Definition: A form of strabismus with both eyes turned inward to a relatively mild degree, usually defined as less than 10 prism diopters.
Comments:
Reference: HP:0025312
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandEsotropia (HP:0000565) 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:0025312HP:0025312Esophoria0HOXB1 CL E G H32115111OMIM:614744Facial paresis, hereditary congenital, 3HP:0040283 - Occasional2
HP:0025312HP:0025312Esophoria0KIDINS220 CL E G H5749829508ORPHA:521390Spastic paraplegia-intellectual disability-nystagmus-obesity syndromeHP:0040282 - Frequent4
HP:0025312HP:0025312Esophoria0MECR CL E G H5110219691OMIM:617282Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities6
HP:0025312HP:0025312Esophoria0MECR CL E G H5110219691ORPHA:508093MEPAN syndrome6
HP:0025312HP:0025312Esophoria0SCN8A CL E G H633410596OMIM:614306Cognitive impairment with or without cerebellar ataxiaHP:0040283 - Occasional357
HP:0025312HP:0025312Esophoria0TBX1 CL E G H689911592OMIM:188400Digeorge syndrome.32


Genes (5) :HOXB1 KIDINS220 MECR SCN8A TBX1

Diseases (6) :OMIM:614744 ORPHA:521390 OMIM:617282 ORPHA:508093 OMIM:614306 OMIM:188400
 

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