Human Phenotype Ontology 
Grandparent Node:
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Abnormal electroretinogram (HP:0000512)help
Parent Node:
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Abnormal full-field electroretinogram (HP:0030466)help
..Starting node
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Abnormal light-adapted electroretinogram (HP:0008275)help
Term ID: 8275
Name: Abnormal light-adapted electroretinogram
Synonym: Abnormal cone-mediated electroretinogram
Definition:
Comments:
Reference: HP:0008275
Genes and Diseases:
 
       Child Nodes:
........expandUndetectable light-adapted electroretinogram (HP:0030465) help
........expandAbnormal light-adapted single flash electroretinogram (HP:0030472) help
................... HP:0030481 Abnormal amplitude of light-adapted single flash electroretinogram
................... HP:0030482 Abnormal timing of light-adapted single flash electroretinogram
........expandAbnormal light-adapted flicker electroretinogram (HP:0030473) help
................... HP:0030479 Abnormal amplitude of light-adapted flicker electroretinogram
................... HP:0030480 Abnormal timing of light-adapted flicker electroretinogram

 Sister Nodes: 
..expandAbnormal dark-adapted electroretinogram (HP:0030469) help
..expandAbnormal light- and dark-adapted electroretinogram (HP:0008323) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0008275HP:0008275Abnormal light-adapted electroretinogram0OPN1SW CL E G H611190900Tritanopia190900C0155017OMIM11771012613522
HP:0008275HP:0008275Abnormal light-adapted electroretinogram0OPN1SW CL E G H611190900Tritanopia190900C0155017OMIM11211012613522
HP:0008275HP:0030465Undetectable light-adapted electroretinogram1OPN1SW CL E G H611190900Tritanopia190900C0155017OMIM11771012613522
HP:0008275HP:0030473Abnormal light-adapted flicker electroretinogram1OPN1SW CL E G H611190900Tritanopia190900C0155017OMIM11771012613522
HP:0008275HP:0030465Undetectable light-adapted electroretinogram1OPN1SW CL E G H611190900Tritanopia190900C0155017OMIM11211012613522
HP:0008275HP:0030473Abnormal light-adapted flicker electroretinogram1OPN1SW CL E G H611190900Tritanopia190900C0155017OMIM11211012613522
HP:0008275HP:0030472Abnormal light-adapted single flash electroretinogram1OPN1SW CL E G H611190900Tritanopia190900C0155017OMIM11771012613522
HP:0008275HP:0030472Abnormal light-adapted single flash electroretinogram1OPN1SW CL E G H611190900Tritanopia190900C0155017OMIM11211012613522
HP:0008275HP:0030480Abnormal timing of light-adapted flicker electroretinogram2OPN1SW CL E G H611190900Tritanopia190900C0155017OMIM11771012613522
HP:0008275HP:0030481Abnormal amplitude of light-adapted single flash electroretinogram2OPN1SW CL E G H611190900Tritanopia190900C0155017OMIM11771012613522
HP:0008275HP:0030480Abnormal timing of light-adapted flicker electroretinogram2OPN1SW CL E G H611190900Tritanopia190900C0155017OMIM11211012613522
HP:0008275HP:0030481Abnormal amplitude of light-adapted single flash electroretinogram2OPN1SW CL E G H611190900Tritanopia190900C0155017OMIM11211012613522
HP:0008275HP:0030482Abnormal timing of light-adapted single flash electroretinogram2OPN1SW CL E G H611190900Tritanopia190900C0155017OMIM11771012613522
HP:0008275HP:0030479Abnormal amplitude of light-adapted flicker electroretinogram2OPN1SW CL E G H611190900Tritanopia190900C0155017OMIM11771012613522
HP:0008275HP:0030482Abnormal timing of light-adapted single flash electroretinogram2OPN1SW CL E G H611190900Tritanopia190900C0155017OMIM11211012613522
HP:0008275HP:0030479Abnormal amplitude of light-adapted flicker electroretinogram2OPN1SW CL E G H611190900Tritanopia190900C0155017OMIM11211012613522
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :OPN1SW

Diseases (1) :190900
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.