G10-G13 Systemic atrophies primarily affecting the central nervous system

 
Chapter VI

Diseases of the nervous system
(G00-G99)

Systemic atrophies primarily affecting the central nervous system
(G10-G13)

G10		Huntington's disease Latin: Morbus Huntington
		Huntington's chorea

G11		Hereditary ataxia Latin: Ataxia hereditaria
		Excludes:	cerebral palsy (G80.-) hereditary and idiopathic neuropathy (G60.-) metabolic disorders (E70-E90)
G11.0		Congenital nonprogressive ataxia Latin: Ataxia non progressiva congenita
G11.1		Early-onset cerebellar ataxia Latin: Ataxia cerebellaris juvenili
		Note:	Onset usually before the age of 20
		Early-onset cerebellar ataxia with: · essential tremor · myoclonus [Hunt's ataxia] · retained tendon reflexes Friedreich's ataxia (autosomal recessive) X-linked recessive spinocerebellar ataxia
G11.2		Late-onset cerebellar ataxia Latin: Ataxia cerebellaris tardiva
		Note:	Onset usually after the age of 20
G11.3		Cerebellar ataxia with defective DNA repair Latin: Ataxia cerebellaris cum detectu DNA
		Ataxia telangiectasia [Louis-Bar]
		Excludes:	Cockayne's syndrome (Q87.1) xeroderma pigmentosum (Q82.1)
G11.4		Hereditary spastic paraplegia Latin: Paraplegia spastica hereditaria
G11.8		Other hereditary ataxias Latin: Ataxiae hereditariae aliae
G11.9		Hereditary ataxia, unspecified Latin: Ataxia hereditaria, non specificata
		Hereditary cerebellar: · ataxia NOS · degeneration · disease · syndrome

G12		Spinal muscular atrophy and related syndromes Latin: Atrophia musculorum spinalis et syndromae affines
G12.0		Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] Latin: Atrophia musculorum spinalis infantilis, typus I (Werding-Hoffman)
G12.1		Other inherited spinal muscular atrophy Latin: Atrophia musculorum spinalis hereditaria alia
		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 Latin: Morbus neuroni motorii
		Familial motor neuron disease Lateral sclerosis: · amyotrophic · primary Progressive: · bulbar palsy · spinal muscular atrophy
G12.8		Other spinal muscular atrophies and related syndromes Latin: Atrophiae musculorum spinales aliae et syndromae affines
G12.9		Spinal muscular atrophy, unspecified Latin: Atrophia musculorum spinalis, non specificata

G13*		Systemic atrophies primarily affecting central nervous system in diseases classified elsewhere Latin: Atrophiae systematis nervosi centralis in morbis aliis
G13.0*		Paraneoplastic neuromyopathy and neuropathy Latin: Neuropathia et neuromyopathia paraneoplastica
		Carcinomatous neuromyopathy (C00-C97+) Sensorial paraneoplastic neuropathy [Denny Brown] (C00-D48+)
G13.1*		Other systemic atrophy primarily affecting central nervous system in neoplastic disease Latin: Atrophia systematis nervosi centralis neoplastica alia
		Paraneoplastic limbic encephalopathy (C00-D48+)
G13.2*		Systemic atrophy primarily affecting central nervous system in myxoedema (E00.1+, E03.-+) Latin: Atrophia systematis nervosi centralis ad cretenismum (E00.1+, E03.-+)
G13.8*		Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere Latin: Atrophia systematis nervosi centralis in morbis aliis

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