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.
Pigmentary pallidal degeneration
Occasional (5-29%)
Friedreich's ataxia
Sturge-Weber sequence
Frequent (30-79%)
Progressive multifocal leukoencephalopathy
Occasional (5-29%)
Arachnoid cyst
Occasional (5-29%)
Retinitis pigmentosa-deafness syndrome
Very frequent (80-99%)
Alstrom syndrome
Occasional (5-29%)
Adrenoleukodystrophy
Frequent (30-79%)
Acromegaly
Occasional (5-29%)
Pituitary dependent hypercortisolism
Very rare (1-4%)
Adult vitelliform macular dystrophy
Frequent (30-79%)
Wagner syndrome
Idiopathic livedo reticularis with systemic involvement
Frequent (30-79%)
Gonadotrophin-secreting pituitary adenoma
Frequent (30-79%)
Acute zonal occult outer retinopathy
Frequent (30-79%)
Hereditary nonpolyposis colon cancer
Occasional (5-29%)
Temporal arteritis
Occasional (5-29%)
Giant cell arteritis
Occasional (5-29%)
Pituicytoma
Frequent (30-79%)
Fatty acid hydroxylase associated neurodegeneration
Frequent (30-79%)
Familial cerebral saccular aneurysm
Frequent (30-79%)
Bothnia retinal dystrophy
Very frequent (80-99%)
Lynch syndrome
Occasional (5-29%)
Livedo reticularis and cerebrovascular accident syndrome
Frequent (30-79%)
Craniosynostosis Boston type
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 12184005
- UMLS CUI
- C3887875
- Fully Specified Name
- Visual field defect (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.