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.
Friedreich's ataxia
Frequent (30-79%)
Progressive multifocal leukoencephalopathy
Very rare (1-4%)
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Frequent (30-79%)
Sialidosis
Dysmorphic sialidosis
Hyperlysinemia
Occasional (5-29%)
Urocanate hydratase deficiency
Always present (100%)
Williams syndrome
Very frequent (80-99%)
Dentatorubropallidoluysian degeneration
Frequent (30-79%)
Alexander's disease
Always present (100%)
Isovaleryl-CoA dehydrogenase deficiency
Occasional (5-29%)
Tay-Sachs disease
Occasional (5-29%)
Deficiency of 3-hydroxyisobutyryl CoA hydrolase
Always present (100%)
Deficiency of neuraminidase
ABL - Abetalipoproteinaemia
Occasional (5-29%)
Troyer syndrome
Always present (100%)
Carbohydrate-deficient glycoprotein syndrome type I
Frequent (30-79%)
Congenital bilateral perisylvian syndrome
Occasional (5-29%)
Medulloblastoma
Frequent (30-79%)
Vanishing white matter disease
Occasional (5-29%)
Fragile X associated tremor ataxia syndrome
Congenital disorder of glycosylation type Ia
Frequent (30-79%)
MEMSA - myoclonic epilepsy myopathy sensory ataxia
Frequent (30-79%)
Ataxia-telangiectasia-like disorder
Frequent (30-79%)
PRICKLE1-related progressive myoclonic epilepsy with ataxia
Quick Facts
- SNOMED CT
- 32566006
- UMLS CUI
- C0234162
- Fully Specified Name
- Dysmetria (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.