Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Niemann-Pick disease, type C
Occasional (5-29%)
Diffuse Lewy body disease
Lafora disease
Frequent (30-79%)
Non-familial hemiplegic migraine
Carcinoma-associated retinopathy
Very rare (1-4%)
Senile dementia of the Lewy body type
Marchiafava-Bignami disease
Occasional (5-29%)
Temporal arteritis
Occasional (5-29%)
Giant cell arteritis
Occasional (5-29%)
Subependymal nodular heterotopia
Occasional (5-29%)
Sporadic Creutzfeldt-Jakob disease
Frequent (30-79%)
Benson syndrome
Occasional (5-29%)
Autosomal dominant late onset Parkinson disease
Occasional (5-29%)
Kufor Rakeb syndrome
Frequent (30-79%)
FFEVF - familial focal epilepsy with variable foci
Occasional (5-29%)
Benign occipital epilepsy
Frequent (30-79%)
Pallidopyramidal syndrome
Frequent (30-79%)
Autosomal dominant epilepsy with auditory features
Occasional (5-29%)
Bilateral parasagittal parieto-occipital polymicrogyria
Occasional (5-29%)
Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome
Occasional (5-29%)
Familial hemiplegic migraine type 1
Quick Facts
- SNOMED CT
- 64269007
- UMLS CUI
- C0233763
- Fully Specified Name
- Visual hallucinations (finding)
- Associated Conditions
- 21
- 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.