Young adult-onset distal hereditary motor neuropathy

disorder

SNOMED 771475006CUI C4749918

Overview

Young adult-onset distal hereditary motor neuropathy 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.

Absent tendon reflexes

Always present (100%)HP:0001284

Distal limb muscle weakness due to peripheral neuropathy

Always present (100%)HP:0002460

Gait disturbance

Always present (100%)HP:0001288

Inability to heel walk

Always present (100%)HP:0009027

Lower limb muscle hypotrophy

Always present (100%)HP:0008944

Cavus foot

Frequent (30-79%)HP:0001761

Dysphonia

Frequent (30-79%)HP:0001618

Loss of distal sensation

Excluded (<1%)HP:0002936

Spinal muscle wasting

HP:0007269

Related Conditions

Chronic nervous system disease(parent)

Autosomal recessive distal hereditary motor neuropathy(parent)

Quick Facts

SNOMED CT: 771475006
UMLS CUI: C4749918
Fully Specified Name: Young adult-onset distal hereditary motor neuropathy (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.