Human Phenotype Ontology 
Grandparent Node:
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Abnormal electroretinogram (HP:0000512)help
Parent Node:
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Abnormal multifocal electroretinogram (HP:0030468)help
..Starting node
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Abnormal paracentral response of multifocal electroretinogram (HP:0030489)help
Term ID: 30489
Name: Abnormal paracentral response of multifocal electroretinogram
Synonym:
Definition:
Comments:
Reference: HP:0030489
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal central response of multifocal electroretinogram (HP:0030488) 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:0030489HP:0030489Abnormal paracentral response of multifocal 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.