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
Frequent (30-79%)
HNSHA due to glucose phosphate isomerase deficiency
Déjérine-Sottas disease
Always present (100%)
Chronic inflammatory demyelinating polyradiculoneuropathy
Very frequent (80-99%)
Bickerstaff's brainstem encephalitis
Occasional (5-29%)
MEMSA - myoclonic epilepsy myopathy sensory ataxia
Occasional (5-29%)
Charcot-Marie-Tooth disease type 4C
Occasional (5-29%)
Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome
Occasional (5-29%)
Autosomal recessive posterior column ataxia and retinitis pigmentosa
Secondary syringomyelia
Frequent (30-79%)
Autosomal dominant Charcot-Marie-Tooth disease type 2V
Frequent (30-79%)
Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 445458007
- UMLS CUI
- C0240991
- Fully Specified Name
- Sensory ataxia (finding)
- Associated Conditions
- 12
- 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.