Overview
Distal hereditary motor neuropathy type V 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.
Distal limb muscle weakness due to peripheral neuropathy
Always present (100%)HP:0002460
Cold-induced hand cramps
Frequent (30-79%)HP:0003435
Distal muscle weakness in lower limbs
Frequent (30-79%)HP:0009053
First dorsal interossei muscle atrophy
Frequent (30-79%)HP:0003426
First dorsal interossei muscle weakness
Frequent (30-79%)HP:0003392
Impaired vibratory sensation
Frequent (30-79%)HP:0002495
Motor polyneuropathy
Frequent (30-79%)HP:0007178
Thenar muscle atrophy
Frequent (30-79%)HP:0003393
Thenar muscle weakness
Frequent (30-79%)HP:0003427
Unsteady walk
Frequent (30-79%)HP:0002317
Upper limb muscle weakness
Frequent (30-79%)HP:0003484
Cavus foot
Occasional (5-29%)HP:0001761
Fallen arches
Occasional (5-29%)HP:0001763
Hammertoe
Occasional (5-29%)HP:0001765
Increased reflexes
Occasional (5-29%)HP:0001347
Pes valgus
Occasional (5-29%)HP:0008081
Abnormal motor nerve conduction velocity
Very rare (1-4%)HP:0040131
Amyotrophy involving the upper limbs
HP:0009129
Distal muscle atrophy, upper and lower limbs
HP:0003693
Peripheral neuropathy
HP:0009830
Related Conditions
Quick Facts
- SNOMED CT
- 1197152005
- UMLS CUI
- C1833308
- Fully Specified Name
- Distal hereditary motor neuropathy type 5 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 20
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.