Human Phenotype Ontology 
Grandparent Node:
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Abnormal dark-adapted electroretinogram (HP:0030469)help
Parent Node:
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Abnormal dark-adapted bright flash electroretinogram (HP:0030470)help
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Abnormal timing of dark-adapted bright flash electroretinogram (HP:0030477)help
Term ID: 30477
Name: Abnormal timing of dark-adapted bright flash electroretinogram
Synonym:
Definition:
Comments:
Reference: HP:0030477
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal amplitude of dark-adapted bright flash electroretinogram (HP:0030478) 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:0030477HP:0030477Abnormal timing of dark-adapted bright flash electroretinogram0 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.