Human Phenotype Ontology 
Grandparent Node:
Abnormal eye physiology (HP:0012373)help
Parent Node:
Abnormality of vision (HP:0000504)help
..Starting node
Bradyopsia (HP:0030511)help
Term ID: 30511
Name: Bradyopsia
Synonym: Difficulty seeing moving objects
Definition: Difficulty in seeing moving objects.
Reference: HP:0030511
Genes and Diseases:
       Child Nodes:

 Sister Nodes: 
..expandAbnormality of binocular vision (HP:0011514) help
..expandAmaurosis fugax (HP:0100576) help
..expandBlurred vision (HP:0000622) help
..expandColor vision defect (HP:0000551) help
..expandDifficulty adjusting to changes in luminance (HP:0030512) help
..expandHemeralopia (HP:0012047) help
..expandMetamorphopsia (HP:0012508) help
..expandNyctalopia (HP:0000662) help
..expandPhotophobia (HP:0000613) help
..expandPhotopsia (HP:0030786) help
..expandPoor visual behavior for age (HP:0025152) help
..expandReduced visual acuity (HP:0007663) help
..expandVisual field defect (HP:0001123) help
..expandVisual impairment (HP:0000505) help
..expandVisual loss (HP:0000572) help
..expandVitreous floaters (HP:0100832) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HP:0030511HP:0030511Bradyopsia0CACNA1A CL E G H77398758ORPHA12511388601011
HP:0030511HP:0030511Bradyopsia0RGS9 CL E G H8787608415Bradyopsia608415C1842073OMIM1310004604067
HP:0030511HP:0030511Bradyopsia0RGS9BP CL E G H388531608415Bradyopsia608415C1842073OMIM1730304607814
HPO disease - gene - phenotype less frequent non-typical associations:

Genes (3) :CACNA1A RGS9 RGS9BP

Diseases (2) :98758 608415

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