Carbon monoxide-induced parkinsonism

disorder

SNOMED 230293003CUI C0393565

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

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

Abnormality of the periventricular white matter

Very frequent (80-99%)HP:0002518

Behavioral changes

Very frequent (80-99%)HP:0000708

Elevated brain choline level by MRS

Very frequent (80-99%)HP:0012706

Memory impairment

Very frequent (80-99%)HP:0002354

Reduced brain N-acetyl aspartate level by MRS

Very frequent (80-99%)HP:0012708

Abnormality of the arm

Frequent (30-79%)HP:0002817

Decreased facial expression

Frequent (30-79%)HP:0004673

Muscle rigidity

Frequent (30-79%)HP:0002063

Slowness of movements

Frequent (30-79%)HP:0002067

Related Conditions

Encephalopathy caused by carbon monoxide(parent)

Toxin-induced parkinsonism(parent)

Quick Facts

SNOMED CT: 230293003
UMLS CUI: C0393565
Fully Specified Name: Carbon monoxide-induced parkinsonism (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 9

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.