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.
Jakob-Creutzfeldt disease
Charcot-Marie-Tooth disease, type IC
Always present (100%)
Coffin-Siris syndrome
Occasional (5-29%)
Friedreich's ataxia
Always present (100%)
Ring chromosome 22 syndrome
Frequent (30-79%)
Adenylosuccinate lyase deficiency
Niemann-Pick disease, type D
Always present (100%)
Progressive multifocal leukoencephalopathy
Frequent (30-79%)
Metachromatic leukodystrophy, congenital type
Frequent (30-79%)
Roussy-Lévy syndrome
Frequent (30-79%)
Metachromatic leukodystrophy, late infantile type
Frequent (30-79%)
Hyperlysinemia
Occasional (5-29%)
Huntington's chorea
Urocanate hydratase deficiency
Very frequent (80-99%)
Mannosidosis
Niemann-Pick disease, type C
Always present (100%)
Gerstmann-Straussler-Scheinker syndrome
Very frequent (80-99%)
Dentatorubropallidoluysian degeneration
Frequent (30-79%)
Sphingolipid activator protein 1 deficiency
Rett's disorder
Marinesco-Sjogren syndrome
Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance
Saccharopinuria
Occasional (5-29%)
Deficiency of ceruloplasmin
Frequent (30-79%)
Deficiency of alpha-mannosidase
Quick Facts
- SNOMED CT
- 25136009
- UMLS CUI
- C0751837
- Fully Specified Name
- Ataxic 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.