Abnormality of visual evoked potentials

Symptom Information:

Symptom ID: HPO:0000649
Synonyms:
Abnormal visual evoked potential [HPO:0000649]
Abnormal visual evoked potentials [HPO:0000649]
Abnormal visual evoked responses [HPO:0000649]
Abnormal visual-evoked potentials [HPO:0000649]
VEP abnormalities [HPO:0000649]
Abnormal Visual evoked potential [Orphanet:5780]
Abnormal visual evoked potential (finding) [Orphanet:5780]
Abnormal visual evoked potential [Orphanet:5780]
Abnormal visual evoked potentials [OMIM:Abnormal visual evoked potentials]
Abnormal visual-evoked potentials [OMIM:Abnormal visual-evoked potentials]
Abnormal VEP/Visual evoked potential [Orphanet:5780]
Visual evoked potentials abnormal [Orphanet:5780]
Visual evoked potentials abnormal [MedDRA:10047549]
Evoked potentials visual abnormal [MedDRA:10047549]
Nonspecific abnormal visually evoked potential [MedDRA:10047549]
VEP's abnormal [MedDRA:10047549]
Visual evoked potentials abnorm. [MedDRA:10047549]
Abnormal VEP [OMIM:Abnormal VEP]
Abnormal visual evoked potential (VEP) [OMIM:Abnormal visual evoked potential (VEP)]
Abnormal visual evoked potentials (1 patient) [OMIM:Abnormal visual evoked potentials (1 patient)]
Abnormal visual evoked potentials (VEP) [OMIM:Abnormal visual evoked potentials (VEP)]
Abnormal visual evoked responses (VEP) [OMIM:Abnormal visual evoked responses (VEP)]
Quality:
Cross references:
Orphanet:5780 "Abnormal VEP/Visual evoked potential" [Orphanet:5780]
OMIM: "Abnormal visual evoked potentials" [OMIM:Abnormal visual evoked potentials]
OMIM: "Abnormal visual-evoked potentials" [OMIM:Abnormal visual-evoked potentials]
OMIM: "Abnormal VEP" [OMIM:Abnormal VEP]
OMIM: "Abnormal visual evoked potential (VEP)" [OMIM:Abnormal visual evoked potential (VEP)]
OMIM: "Abnormal visual evoked potentials (1 patient)" [OMIM:Abnormal visual evoked potentials (1 patient)]
OMIM: "Abnormal visual evoked potentials (VEP)" [OMIM:Abnormal visual evoked potentials (VEP)]
OMIM: "Abnormal visual evoked responses (VEP)" [OMIM:Abnormal visual evoked responses (VEP)]
UMLS:C0522214 "Abnormal visual evoked potential" [Orphanet:5780]
Is a (Direct Parents):
HPO         Abnormality of vision
Orphanet Abnormality of the eye
MedDRA Neurologic diagnostic procedures
HPO         Abnormality of pattern visual evoked potentials
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye physiology(HPO:0012373)
             Abnormality of vision(HPO:0000504)
                Abnormality of visual evoked potentials(HPO:0000649)
MedDRA:
Investigations(MedDRA:10022891)
    Neurological, special senses and psychiatric investigations(MedDRA:10029295)
       Neurologic diagnostic procedures(MedDRA:10029285)
          Abnormality of visual evoked potentials(HPO:0000649)
Database Frequency: 34 / 7739
Resource:

All diseases associated with this symptom:

ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME (OMIM:231550)
AICA-ribosiduria (Orphanet:250977)
ALG1-CDG (Orphanet:79327)
Alpers syndrome (Orphanet:726)
Ataxia with vitamin E deficiency (Orphanet:96)
Autosomal dominant optic atrophy plus syndrome (Orphanet:1215)
Autosomal recessive malignant osteopetrosis (Orphanet:667)
CADASIL (Orphanet:136)
COCKAYNE SYNDROME A (OMIM:216400)
COCKAYNE SYNDROME, TYPE III (OMIM:216411)
Canavan disease (Orphanet:141)
Charcot-Marie-Tooth disease type 4D (Orphanet:99950)
Cockayne syndrome (Orphanet:191)
Congenital ichthyosis - intellectual deficit - spastic quadriplegia (Orphanet:352333)
Cortical blindness - intellectual deficit - polydactyly (Orphanet:1389)
Early myoclonic encephalopathy (Orphanet:1935)
Friedreich ataxia 1 (OMIM:229300)
Hereditary motor and sensory neuropathy type 6 (Orphanet:90120)
Hermansky-Pudlak syndrome (Orphanet:79430)
Infantile neuroaxonal dystrophy (Orphanet:35069)
Infantile neuronal ceroid lipofuscinosis (Orphanet:79263)
Juvenile neuronal ceroid lipofuscinosis (Orphanet:79264)
Late infantile neuronal ceroid lipofuscinosis (Orphanet:168491)
Leber hereditary optic neuropathy (Orphanet:104)
MELAS (Orphanet:550)
Micro syndrome (Orphanet:2510)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria (Orphanet:1933)
Mohr-Tranebjaerg syndrome (Orphanet:52368)
Oculocutaneous albinism type 1A (Orphanet:79431)
Pelizaeus-Merzbacher disease (Orphanet:702)
Peroxisomal acyl-CoA oxidase deficiency (Orphanet:2971)
Ruvalcaba syndrome (Orphanet:3121)
Severe Canavan disease (Orphanet:314911)
Triple A syndrome (Orphanet:869)