Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Decreased distal sensory nerve action potential
Always present (100%)HP:0007230
Decreased motor nerve conduction velocity
Always present (100%)HP:0003431
Decreased nerve conduction velocity
Always present (100%)HP:0000762
Hypoaesthesia
Always present (100%)HP:0033748
Inability to coordinate movements when walking
Always present (100%)HP:0002066
Nerve damage causing decreased feeling and movement
Always present (100%)HP:0007141
Peripheral nerve disease
Always present (100%)HP:0001271
Ataxia
Frequent (30-79%)HP:0001251
Cavus foot
Frequent (30-79%)HP:0001761
Paresthesia
Frequent (30-79%)HP:0003401
Positive Romberg sign
Frequent (30-79%)HP:0002403
Distal limb muscle weakness due to peripheral neuropathy
HP:0002460
Distal muscle atrophy, upper and lower limbs
HP:0003693
Hypertrophic nerve changes
HP:0003382
Hyporeflexia
HP:0001265
Loss of distal sensation
HP:0002936
Onion bulb formation
HP:0003383
Segmental peripheral demyelination/remyelination
HP:0003481
Related Conditions
Quick Facts
- SNOMED CT
- 4183003
- UMLS CUI
- C0270913
- Fully Specified Name
- Charcot-Marie-Tooth disease, type IC (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 18
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.