Human Phenotype Ontology 
Grandparent Node:
Abnormal visual fixation (HP:0025404)help
Parent Node:
Eccentric visual fixation (HP:0025549)help
..Starting node
Peripheral fixation (HP:0031769)help
Term ID: 31769
Name: Peripheral fixation
Definition: Fixation of an object in a peripheral area of the retina.
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 August 2021 release.