Abnormality of visual evoked potentials
Symptom Information:
Symptom ID: | HPO:0000649 | ||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |