Human Phenotype Ontology 
Grandparent Node:
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Abnormality of pattern visual evoked potentials (HP:0030455)help
Parent Node:
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Abnormality of pattern reversal visual evoked potentials (HP:0100289)help
..Starting node
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Abnormal amplitude of pattern reversal visual evoked potentials (HP:0000650)help
Term ID: 650
Name: Abnormal amplitude of pattern reversal visual evoked potentials
Synonym:
Definition:
Comments:
Reference: HP:0000650
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal timing of pattern reversal visual evoked potentials (HP:0030460) help
..expandAsymmetrical distribution of pattern reversal visual evoked potentials (HP:0030464) 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:0000650HP:0000650Abnormal amplitude of pattern reversal visual evoked potentials0OPA1 CL E G H49768140OMIM:165500Optic atrophy 1.214
HP:0000650HP:0000650Abnormal amplitude of pattern reversal visual evoked potentials0OPA1 CL E G H49768140OMIM:125250Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy.214


Genes (1) :OPA1

Diseases (2) :OMIM:165500 OMIM:125250
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.