Human Phenotype Ontology 
Grandparent Node:
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Abnormality of eye movement (HP:0000496)help
Parent Node:
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Abnormal visual fixation (HP:0025404)help
..Starting node
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Eccentric visual fixation (HP:0025549)help
Term ID: 25549
Name: Eccentric visual fixation
Synonym: Eccentric fixation
Definition: A uniocular condition in which there is fixation of an object by a point other than the fovea. This point adopts the principal visual direction. The degree of the eccentric fixation is defined by its distance from the fovea in degrees.
Comments:
Reference: HP:0025549
Genes and Diseases:
 
       Child Nodes:
........expandParafoveal fixation (HP:0031768) help
........expandPeripheral fixation (HP:0031769) help
........expandAbsolute eccentric fixation (HP:0500072) help

 Sister Nodes: 
..expandVisual fixation instability (HP:0025405) 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:0025549HP:0025549Eccentric visual fixation0ATF6 CL E G H22926791ORPHA:49382AchromatopsiaHP:0040283 - Occasional10
HP:0025549HP:0025549Eccentric visual fixation0CNGA3 CL E G H12612150ORPHA:49382AchromatopsiaHP:0040283 - Occasional82
HP:0025549HP:0025549Eccentric visual fixation0CNGB3 CL E G H547142153ORPHA:49382AchromatopsiaHP:0040283 - Occasional194
HP:0025549HP:0025549Eccentric visual fixation0GNAT2 CL E G H27804394ORPHA:49382AchromatopsiaHP:0040283 - Occasional19
HP:0025549HP:0025549Eccentric visual fixation0OFD1 CL E G H84812567OMIM:300424Retinitis pigmentosa 23201
HP:0025549HP:0025549Eccentric visual fixation0PDE6C CL E G H51468787ORPHA:49382AchromatopsiaHP:0040283 - Occasional80
HP:0025549HP:0025549Eccentric visual fixation0PDE6H CL E G H51498790ORPHA:49382AchromatopsiaHP:0040283 - Occasional14
HP:0025549HP:0025549Eccentric visual fixation0RPGR CL E G H610310295ORPHA:49382AchromatopsiaHP:0040283 - Occasional200
HP:0025549HP:0500072Absolute eccentric fixation1 CL E G H
HP:0025549HP:0031769Peripheral fixation1 CL E G H
HP:0025549HP:0031768Parafoveal fixation1 CL E G H


Genes (8) :ATF6 CNGA3 CNGB3 GNAT2 OFD1 PDE6C PDE6H RPGR

Diseases (2) :ORPHA:49382 OMIM:300424
 

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