Overview
Abnormal visual evoked potential is a finding that may indicate an underlying health condition requiring clinical evaluation.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Ruvalcaba syndrome
Occasional (5-29%)
Tyrosinase-negative oculocutaneous albinism
Frequent (30-79%)
Hermansky-Pudlak syndrome
Frequent (30-79%)
Friedreich's ataxia
Progressive sclerosing poliodystrophy
Metachromatic leukodystrophy, adult type
Occasional (5-29%)
Metachromatic leukodystrophy, congenital type
Occasional (5-29%)
Globoid cell leukodystrophy, late-onset
Frequent (30-79%)
Metachromatic leukodystrophy, juvenile type
Frequent (30-79%)
Glucocorticoid deficiency with achalasia
Fundus flavimaculatus
Very frequent (80-99%)
Metachromatic leukodystrophy, late infantile type
Occasional (5-29%)
Infantile neuroaxonal dystrophy
Frequent (30-79%)
Leber's optic atrophy
Occasional (5-29%)
Cholestanol storage disease
Frequent (30-79%)
Pelizaeus-Merzbacher disease
Frequent (30-79%)
Stargardt's disease
Very frequent (80-99%)
Spongy degeneration of central nervous system
Frequent (30-79%)
Merosin deficient congenital muscular dystrophy
Occasional (5-29%)
Hereditary sensory and motor neuropathy, type VI
Galactosylceramide lipidosis
Very frequent (80-99%)
Galactocerebroside beta-galactosidase deficiency - early onset
Very frequent (80-99%)
Acyl-CoA oxidase deficiency
Very frequent (80-99%)
Odontotrichomelic syndrome
Frequent (30-79%)
Infantile malignant osteopetrosis
Very frequent (80-99%)
Quick Facts
- SNOMED CT
- 102968003
- UMLS CUI
- C0522214
- Fully Specified Name
- Abnormal visual evoked potential (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.