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.
Postencephalitic parkinsonism
Frequent (30-79%)
Japanese encephalitis virus disease
Frequent (30-79%)
Manganese pneumonitis
Very frequent (80-99%)
Deficiency of ceruloplasmin
Diurnal dystonia
Occasional (5-29%)
Dravet syndrome
Frequent (30-79%)
Poisoning by manganese
Very frequent (80-99%)
Thiamine transporter-2 deficiency
Very frequent (80-99%)
Autosomal dominant dopa responsive dystonia
Occasional (5-29%)
Early onset parkinsonism and intellectual disability syndrome
Spinocerebellar ataxia type 21
Spinocerebellar ataxia type 19
Occasional (5-29%)
Spinocerebellar ataxia type 37
Very frequent (80-99%)
Dopamine transporter deficiency syndrome
Frequent (30-79%)
X-linked parkinsonism with spasticity syndrome
Very frequent (80-99%)
Autosomal dominant progressive external ophthalmoplegia
Occasional (5-29%)
Autosomal recessive progressive external ophthalmoplegia
Occasional (5-29%)
Familial infantile bilateral striatal necrosis
Occasional (5-29%)
Spinocerebellar ataxia type 43
Frequent (30-79%)
Idiopathic catatonia
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 55630000
- UMLS CUI
- C0151564
- Fully Specified Name
- Cogwheel muscle rigidity (finding)
- Associated Conditions
- 20
- 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.