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.
Pigmentary pallidal degeneration
Always present (100%)
Agenesis of corpus callosum
Occasional (5-29%)
Chorea acanthocytosis syndrome
Frequent (30-79%)
Familial dysautonomia
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Frequent (30-79%)
Metachromatic leukodystrophy, juvenile type
Occasional (5-29%)
Rubinstein-Taybi syndrome
Always present (100%)
Hyperlysinemia
Occasional (5-29%)
Williams syndrome
Frequent (30-79%)
Alstrom syndrome
Occasional (5-29%)
Adrenoleukodystrophy
Sotos' syndrome
Isaacs syndrome
Primary lateral sclerosis
Frequent (30-79%)
Wilson's disease
Oromandibular-limb hypogenesis spectrum
20p partial trisomy syndrome
Very frequent (80-99%)
Tay-Sachs disease
Frequent (30-79%)
Deficiency of uridyl transferase
Occasional (5-29%)
Deficiency of phosphoriboisomerase
Always present (100%)
Westphal-Strumpell syndrome
Benign myoclonic epilepsy in infancy
Frequent (30-79%)
Acute liver failure
Occasional (5-29%)
Diurnal dystonia
Frequent (30-79%)
Dravet syndrome
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 281016006
- UMLS CUI
- C0520966
- Fully Specified Name
- Incoordination (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.