Certain infectious and parasitic diseases
Certain infectious and parasitic diseases Certain infectious and parasitic diseases
G11.9 Hereditary ataxia, unspecified Hereditary cerebellar: · ataxia NOS · degeneration · disease · syndrome G12 Spinal muscular atrophy and related syndromes G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] G12.1 Other inherited spinal muscular atrophy Progressive bulbar palsy of childhood [Fazio-Londe] Spinal muscular atrophy: · adult form · childhood form, type II · distal · juvenile form, type III [Kugelberg-Welander] · scapuloperoneal form G12.2 Motor neuron disease Familial motor neuron disease Lateral sclerosis: · amyotrophic · primary Progressive: · bulbar palsy · spinal muscular atrophy G12.8 Other spinal muscular atrophies and related syndromes G12.9 Spinal muscular atrophy, unspecified G13* Systemic atrophies primarily affecting central nervous system in diseases classified elsewhere G13.0* Paraneoplastic neuromyopathy and neuropathy Carcinomatous neuromyopathy ( C00-C97† ) Sensorial paraneoplastic neuropathy [Denny Brown] ( C00-D48† ) G13.1* Other systemic atrophy primarily affecting central nervous system in neoplastic disease Paraneoplastic limbic encephalopathy ( C00-D48† ) G13.2* G13.8* Systemic atrophy primarily affecting central nervous system in myxoedema ( E00.1† , E03.-† ) Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere 236 WHO’s ICD-10
Extrapyramidal and movement disorders (G20-G26) G20 Parkinson's disease Hemiparkinsonism Paralysis agitans Parkinsonism or Parkinson's disease: · NOS · idiopathic · primary G21 Secondary parkinsonism G21.0 Malignant neuroleptic syndrome Use additional external cause code (Chapter XX), if desired, to identify drug. G21.1 Other drug-induced secondary parkinsonism Use additional external cause code (Chapter XX), if desired, to identify drug. G21.2 Secondary parkinsonism due to other external agents Use additional external cause code (Chapter XX), if desired, to identify external agent. G21.3 Postencephalitic parkinsonism G21.8 Other secondary parkinsonism G21.9 Secondary parkinsonism, unspecified G22* Parkinsonism in diseases classified elsewhere Syphilitic parkinsonism ( A52.1† ) G23 Other degenerative diseases of basal ganglia Excludes: multi-system degeneration ( G90.3 ) G23.0 Hallervorden-Spatz disease Pigmentary pallidal degeneration G23.1 Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski] G23.2 Striatonigral degeneration G23.8 Other specified degenerative diseases of basal ganglia Calcification of basal ganglia G23.9 Degenerative disease of basal ganglia, unspecified G24 Dystonia Includes: dyskinesia Excludes: athetoid cerebral palsy ( G80.3 ) G24.0 Drug-induced dystonia Use additional external cause code (Chapter XX), if desired, to identify drug. G24.1 Idiopathic familial dystonia Idiopathic dystonia NOS G24.2 Idiopathic nonfamilial dystonia G24.3 Spasmodic torticollis Excludes: torticollis NOS ( M43.6 ) Version for 2007 237
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G11.9 Hereditary ataxia, unspecified<br />
Hereditary cerebellar:<br />
· ataxia NOS<br />
· degeneration<br />
· disease<br />
· syndrome<br />
G12 Spinal muscular atrophy <strong>and</strong> related syndromes<br />
G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]<br />
G12.1 Other inherited spinal muscular atrophy<br />
Progressive bulbar palsy of childhood [Fazio-Londe]<br />
Spinal muscular atrophy:<br />
· adult form<br />
· childhood form, type II<br />
· distal<br />
· juvenile form, type III [Kugelberg-Wel<strong>and</strong>er]<br />
· scapuloperoneal form<br />
G12.2 Motor neuron disease<br />
Familial motor neuron disease<br />
Lateral sclerosis:<br />
· amyotrophic<br />
· primary<br />
Progressive:<br />
· bulbar palsy<br />
· spinal muscular atrophy<br />
G12.8 Other spinal muscular atrophies <strong>and</strong> related syndromes<br />
G12.9 Spinal muscular atrophy, unspecified<br />
G13* Systemic atrophies primarily affecting central nervous system<br />
in <strong>diseases</strong> classified elsewhere<br />
G13.0* Paraneoplastic neuromyopathy <strong>and</strong> neuropathy<br />
Carcinomatous neuromyopathy ( C00-C97† )<br />
Sensorial paraneoplastic neuropathy [Denny Brown] ( C00-D48† )<br />
G13.1*<br />
Other systemic atrophy primarily affecting central nervous system in<br />
neoplastic disease<br />
Paraneoplastic limbic encephalopathy ( C00-D48† )<br />
G13.2*<br />
G13.8*<br />
Systemic atrophy primarily affecting central nervous system in myxoedema<br />
( E00.1† , E03.-† )<br />
Systemic atrophy primarily affecting central nervous system in other<br />
<strong>diseases</strong> classified elsewhere<br />
236 WHO’s ICD-10
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