Human Phenotype Ontology 
Grandparent Node:
expand
Abnormal electroretinogram (HP:0000512)help
Parent Node:
expand
Abnormal pattern electroretinogram (HP:0030467)help
..Starting node
..expand
Abnormal timing of pattern electroretinogram (HP:0030486)help
Term ID: 30486
Name: Abnormal timing of pattern electroretinogram
Synonym:
Definition:
Comments:
Reference: HP:0030486
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal amplitude of pattern electroretinogram (HP:0030485) help
..expandAbnormal P50/N95 ratio of pattern electroretinogram (HP:0030487) help
..expandUndetectable pattern electroretinogram (HP:0030844) 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:0030486HP:0030486Abnormal timing of pattern 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 December 15 2022 release.