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Primary dystonia (G24.105) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Idiopathic torsion dystonia (G24.104) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Dopa-responsive dystonia (G24.103) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Idiopathic dystonia (G24.102) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Idiopathic familial dystonia (G24.100x002) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Idiopathic familial dystonia (G24.100) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Drug-induced dystonia (G24.000x001) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Drug-induced dystonia (G24.000) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Basal-ganglia degenerative disease (G23.900) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Corticobasal degeneration (G23.803) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled.
Primary basal-ganglia calcification (G23.802) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compiled
Olivopontocerebellar atrophy is progressive cerebellar ataxia with parkinsonism/autonomic failure (MSA-C); no cure, supportive/rehab.
神经内科Guam ALS-parkinsonism-dementia complex (G23.800x007) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being c
Dentatorubropallidoluysian atrophy (G23.800x006) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is being compi
Familial idiopathic basal-ganglia calcification (Fahr disease) (G23.800x005) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological
Other specified basal-ganglia degenerative disease (G23.800) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed pathological introduction is
Striatonigral degeneration is atypical parkinsonism with severe rigidity, poor levodopa response, autonomic/cerebellar features (MSA-P); supportive care.
神经内科Progressive supranuclear palsy (Steele-Richardson-Olszewski) is atypical parkinsonism with axial rigidity, supranuclear gaze palsy, falls, dementia; poor levodopa response, supportive.
神经内科Progressive supranuclear ophthalmoplegia (Steele-Richardson-Olszewski) (G23.100) is a disease entity listed in the National Clinical Version 2.0 of the Disease Classification and Codes standard issued by the National Health Commission; a detailed patholog
Hallervorden-Spatz disease (NBIA/PKAN) is inherited childhood progressive dystonia/parkinsonism/dementia with iron deposition in globus pallidus; no cure, supportive.
神经内科
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