Overview
Distal hereditary motor neuropathy type 1 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.
Upper limb muscle weakness
Always present (100%)HP:0003484
Cavus foot
HP:0001761
Chronic axonal neuropathy
HP:0007267
Decreased vibration sense in feet
HP:0006938
Distal muscle atrophy, upper and lower limbs
HP:0003693
Extensor plantar responses
HP:0003487
Hammertoe
HP:0001765
Hypertonia
HP:0001276
Weakness of outermost muscles
HP:0002460
Quick Facts
- SNOMED CT
- 770630005
- UMLS CUI
- C1866784
- Fully Specified Name
- Distal hereditary motor neuropathy type 1 (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.