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
Occasional (5-29%)
Corticobasal degeneration
Frequent (30-79%)
Postencephalitic parkinsonism
Occasional (5-29%)
African trypanosomiasis
Occasional (5-29%)
Progressive supranuclear ophthalmoplegia
Occasional (5-29%)
Lethal multiple pterygium syndrome
Trypanosomiasis
Occasional (5-29%)
Manganese pneumonitis
Frequent (30-79%)
Deficiency of ceruloplasmin
Occasional (5-29%)
Progressive supranuclear palsy
Occasional (5-29%)
Pena-Shokeir syndrome type I
Very frequent (80-99%)
Poisoning by manganese
Frequent (30-79%)
Perry syndrome
Always present (100%)
Fowler's syndrome
Lethal congenital contracture syndrome type 2
Autosomal dominant late onset Parkinson disease
Frequent (30-79%)
Spinocerebellar ataxia type 21
Frequent (30-79%)
Spinocerebellar ataxia type 27
Very rare (1-4%)
Kufor Rakeb syndrome
Congenital disorder of glycosylation type 1j
Very rare (1-4%)
Atypical juvenile parkinsonism
Frequent (30-79%)
Static encephalopathy of childhood with neurodegeneration in adulthood
Frequent (30-79%)
Sporadic adult-onset ataxia of unknown etiology
Occasional (5-29%)
Perinatal lethal Gaucher disease
Quick Facts
- SNOMED CT
- 33994004
- UMLS CUI
- C0085623
- Fully Specified Name
- Akinesia (finding)
- Associated Conditions
- 24
- 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.