Human Phenotype Ontology 
Grandparent Node:
expandVisual field defect (HP:0001123)help
Parent Node:
expandScotoma (HP:0000575)help
..Starting node
..expandScintillating scotoma (HP:0010822)help
Term ID: 10822
Name: Scintillating scotoma
Synonym:
Definition: A scintillating scotoma is a common visual aura that can preced a migraine, whereby a spot of flickering light near the center of the visual fields occurs. The spot prevents vision, and is thus termed scotoma. The scotoma can extend into one or more shimmering arcs of white or colored flashing lights.
Comments:
Reference: HP:0010822
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandArcuate scotoma (HP:0030530) help
..expandCentral scotoma (HP:0000603) help
..expandCentrocecal scotoma (HP:0000576) help
..expandParacentral scotoma (HP:0030528) help
..expandPericentral scotoma (HP:0007761) help
..expandRing scotoma (HP:0030529) 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:0010822HP:0010822Scintillating scotoma0 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 December 15 2022 release.