Human Phenotype Ontology 
Grandparent Node:
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Abnormal visual electrophysiology (HP:0030453)help
Parent Node:
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Abnormality of visual evoked potentials (HP:0000649)help
..Starting node
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Undetectable visual evoked potentials (HP:0007965)help
Term ID: 7965
Name: Undetectable visual evoked potentials
Synonym: Absence of visual evoked potentials; Non-detectable VEP; Undetectable VEP
Definition:
Comments:
Reference: HP:0007965
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal flash visual evoked potentials (HP:0007928) help
..expandAbnormality of pattern visual evoked potentials (HP:0030455) 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:0007965HP:0007965Undetectable visual evoked potentials0ATP1A3 CL E G H478801OMIM:601338Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss150
HP:0007965HP:0007965Undetectable visual evoked potentials0COQ2 CL E G H2723525223ORPHA:255249Leigh syndrome with nephrotic syndromeHP:0040283 - Occasional54
HP:0007965HP:0007965Undetectable visual evoked potentials0COX6B1 CL E G H13402280OMIM:619051MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 7; MC4DN710
HP:0007965HP:0007965Undetectable visual evoked potentials0MPDU1 CL E G H95267207ORPHA:79323MPDU1-CDG32
HP:0007965HP:0007965Undetectable visual evoked potentials0NDUFS4 CL E G H47247711OMIM:252010Mitochondrial complex I deficiency, nuclear type 127
HP:0007965HP:0007965Undetectable visual evoked potentials0OSTM1 CL E G H2896221652OMIM:259720Osteopetrosis, autosomal recessive 573
HP:0007965HP:0007965Undetectable visual evoked potentials0PDSS2 CL E G H5710723041ORPHA:255249Leigh syndrome with nephrotic syndromeHP:0040283 - Occasional54
HP:0007965HP:0007965Undetectable visual evoked potentials0PRPS1 CL E G H56319462ORPHA:423479X-linked intellectual disability-limb spasticity-retinal dystrophy-diabetes insipidus syndromeHP:0040282 - Frequent49
HP:0007965HP:0007965Undetectable visual evoked potentials0RAB3GAP2 CL E G H2578217168OMIM:614225Warburg micro syndrome 2.135
HP:0007965HP:0007965Undetectable visual evoked potentials0RDH11 CL E G H5110917964ORPHA:436245Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndromeHP:0040282 - Frequent2
HP:0007965HP:0007965Undetectable visual evoked potentials0ZNHIT3 CL E G H932612309OMIM:260565Peho syndrome1


Genes (11) :ATP1A3 COQ2 COX6B1 MPDU1 NDUFS4 OSTM1 PDSS2 PRPS1 RAB3GAP2 RDH11 ZNHIT3

Diseases (10) :OMIM:601338 ORPHA:255249 OMIM:619051 ORPHA:79323 OMIM:252010 OMIM:259720 ORPHA:423479 OMIM:614225 ORPHA:436245 OMIM:260565
 

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