Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Charcot-Marie-Tooth disease, type IA
Charcot-Marie-Tooth disease, type IB
Distal muscular dystrophy
Frequent (30-79%)
Leprosy
Occasional (5-29%)
Amyotrophic lateral sclerosis
Occasional (5-29%)
Déjérine-Sottas disease
Hereditary sensory and motor neuropathy, type VI
Occasional (5-29%)
Giant axonal neuropathy
ABL - Abetalipoproteinaemia
Occasional (5-29%)
Landau-Kleffner syndrome
Occasional (5-29%)
Autosomal dominant sensory neuropathy
Frequent (30-79%)
Subacute idiopathic demyelinating polyradiculoneuropathy
Occasional (5-29%)
Hereditary sensory and autonomic neuropathy type I
Frequent (30-79%)
Charcot-Marie-Tooth disease, type I
Facioscapulohumeral muscular dystrophy
Frequent (30-79%)
Tibial muscular dystrophy
Frequent (30-79%)
Hypermanganesemia with dystonia, polycythaemia, and cirrhosis
Hereditary inclusion body myopathy
Frequent (30-79%)
Autosomal recessive axonal neuropathy with neuromyotonia
Occasional (5-29%)
Charcot-Marie-Tooth disease and deafness
Occasional (5-29%)
Charcot-Marie-Tooth disease type 4B2
Occasional (5-29%)
Autosomal dominant Charcot-Marie-Tooth disease type 2B
Always present (100%)
Autosomal dominant Charcot-Marie-Tooth disease type 2E
Occasional (5-29%)
Autosomal dominant Charcot-Marie-Tooth disease type 2I
Autosomal dominant Charcot-Marie-Tooth disease type 2J
Quick Facts
- SNOMED CT
- 27253007
- UMLS CUI
- C0427149
- Fully Specified Name
- Foot-drop gait (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.