Autosomal dominant slowed nerve conduction velocity

disorder

SNOMED 764854006CUI C1842357

Overview

Autosomal dominant slowed nerve conduction velocity 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.

Decreased nerve conduction velocity

HP:0000762

Onion bulb formation

HP:0003383

Peripheral demyelination

HP:0011096

Related Conditions

Autosomal dominant hereditary disorder(parent)

Congenital disease(parent)

Hereditary motor and sensory neuropathy(parent)

Quick Facts

SNOMED CT: 764854006
UMLS CUI: C1842357
Fully Specified Name: Autosomal dominant slowed nerve conduction velocity (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 3

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.