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.
Dandy-Walker syndrome
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Frequent (30-79%)
Urocanate hydratase deficiency
Very frequent (80-99%)
Adrenoleukodystrophy
Gerstmann-Straussler-Scheinker syndrome
Cytochrome-c oxidase deficiency
Always present (100%)
Dentatorubropallidoluysian degeneration
Frequent (30-79%)
Rett's disorder
Azorean disease
Deficiency of succinic dehydrogenase
Always present (100%)
Deficiency of 3-hydroxyisobutyryl CoA hydrolase
Frequent (30-79%)
Complex II deficiency
Always present (100%)
Neonatal pseudo-hydrocephalic progeroid syndrome
Multiple symmetrical lipomatosis
Vanishing white matter disease
Frequent (30-79%)
Christianson syndrome
Very frequent (80-99%)
Hypermanganesemia with dystonia, polycythaemia, and cirrhosis
Occasional (5-29%)
Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation
Very rare (1-4%)
Spinocerebellar ataxia type 36
Very frequent (80-99%)
Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1
Spinocerebellar ataxia type 1
Spinocerebellar ataxia type 6
Occasional (5-29%)
Spinocerebellar ataxia type 29
Always present (100%)
Spinocerebellar ataxia type 15/16
Always present (100%)
Cerebellar ataxia Cayman type
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 250067008
- UMLS CUI
- C0427190
- Fully Specified Name
- Truncal ataxia (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.