Leukoencephalopathy with mild cerebellar ataxia and white matter edema

disorder

SNOMED 768663003CUI C4554120

Overview

Leukoencephalopathy with mild cerebellar ataxia and white matter edema is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Appendicular ataxia

Always present (100%)HP:0002070

Action tremor

Frequent (30-79%)HP:0002345

Damaged optic nerve

Frequent (30-79%)HP:0001138

Headache

Frequent (30-79%)HP:0002315

Inability to coordinate movements when walking

Frequent (30-79%)HP:0002066

Partial loss of field of vision

Frequent (30-79%)HP:0001123

Chorioretinal atrophy

Occasional (5-29%)HP:0000533

Choroidal neovascular membrane

Occasional (5-29%)HP:0011506

Retinoschisis

Occasional (5-29%)HP:0030502

Leukoencephalopathy

HP:0002352

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Leukoencephalopathy(parent)

Cerebellar ataxia(parent)

Hereditary ataxia(parent)

Quick Facts

SNOMED CT: 768663003
UMLS CUI: C4554120
Fully Specified Name: Leukoencephalopathy with mild cerebellar ataxia and white matter edema (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 10

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.