Overview
Dysdiadokokinesia is a finding that may indicate an underlying health condition requiring clinical evaluation.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Friedreich's ataxia
Occasional (5-29%)
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Frequent (30-79%)
Dentatorubropallidoluysian degeneration
Frequent (30-79%)
Ataxia-telangiectasia syndrome
Frequent (30-79%)
Gamma-glutamyl transpeptidase deficiency
Frequent (30-79%)
Oromandibular-limb hypogenesis spectrum
Diurnal dystonia
Frequent (30-79%)
Ataxic cerebral palsy
Fragile X associated tremor ataxia syndrome
MEMSA - myoclonic epilepsy myopathy sensory ataxia
Frequent (30-79%)
Ataxia-telangiectasia-like disorder
Occasional (5-29%)
Hypermanganesemia with dystonia, polycythaemia, and cirrhosis
Frequent (30-79%)
Fatty acid hydroxylase associated neurodegeneration
Familial isolated vitamin E deficiency
Frequent (30-79%)
Spinocerebellar ataxia type 7
Frequent (30-79%)
Spinocerebellar ataxia type 1
Occasional (5-29%)
Spinocerebellar ataxia type 2
Spinocerebellar ataxia type 10
Frequent (30-79%)
Autosomal dominant dopa responsive dystonia
Frequent (30-79%)
Spinocerebellar ataxia type 29
Frequent (30-79%)
Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome
Always present (100%)
Choroideremia with deafness and obesity syndrome
Occasional (5-29%)
Brain dopamine-serotonin vesicular transport disease
Very frequent (80-99%)
Spinocerebellar ataxia type 12
Spinocerebellar ataxia type 18
Quick Facts
- SNOMED CT
- 23133003
- UMLS CUI
- C0234979
- Fully Specified Name
- Dysdiadochokinesis (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.