Human Phenotype Ontology 
Grandparent Node:
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Abnormal visual fixation (HP:0025404)help
Parent Node:
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Eccentric visual fixation (HP:0025549)help
..Starting node
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Peripheral fixation (HP:0031769)help
Term ID: 31769
Name: Peripheral fixation
Synonym:
Definition: Fixation of an object in a peripheral area of the retina.
Comments:
Reference: HP:0031769
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbsolute eccentric fixation (HP:0500072) help
..expandParafoveal fixation (HP:0031768) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031769HP:0031769Peripheral fixation0 CL E G H


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.