Autosomal dominant distal hereditary motor neuropathy

disorder

SNOMED 1156837002CUI C5548212

Overview

Autosomal dominant distal hereditary motor neuropathy is a disorder.

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

Related Conditions

Silver disease(child)

Distal hereditary motor neuropathy type 1(child)

Distal hereditary motor neuropathy type 7(child)

Autosomal dominant congenital benign spinal muscular atrophy(child)

Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome(child)

Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome(child)

Distal hereditary motor neuropathy type V(child)

Autosomal dominant distal spinal muscular atrophy type 2(child)

Autosomal dominant hereditary disorder(parent)

Hereditary disorder of nervous system(parent)

Motor peripheral neuropathy(parent)

Quick Facts

SNOMED CT: 1156837002
UMLS CUI: C5548212
Fully Specified Name: Autosomal dominant distal hereditary motor neuropathy (disorder)
Specialists: 0
Diagnostic Biomarkers: 0

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.