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Charcot-Marie-Tooth disease type 4B1

disorder
SNOMED 715803003CUI C1832399

Overview

Charcot-Marie-Tooth disease type 4B1 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 muscle atrophy, upper and lower limbs
Always present (100%)HP:0003693
Abnormal auditory evoked potentials
HP:0006958
Cobb angle greater than ten degrees
HP:0002650
Decreased motor nerve conduction velocity
HP:0003431
Distal limb muscle weakness due to peripheral neuropathy
HP:0002460
Facial muscle weakness of muscles innervated by CN VII
HP:0010628
Fetal foot inversion
HP:0001762
Irregular myelin foldings
HP:0004336
Irregular myelin loops
HP:0007208
Loss of distal sensation
HP:0002936
No development of motor milestones
HP:0001270
Proximal limb muscle weakness
HP:0003701

Quick Facts

SNOMED CT
715803003
UMLS CUI
C1832399
Fully Specified Name
Charcot-Marie-Tooth disease type 4B1 (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
12
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.