Diseases

F78A9

Other genetic related intellectual disability

F800

Phonological disorder

F801

Expressive language disorder

F802

Mixed receptive-expressive language disorder

F804

Speech and language development delay due to hearing loss

F8081

Childhood onset fluency disorder

F8082

Social pragmatic communication disorder

F8089

Other developmental disorders of speech and language

F809

Developmental disorder of speech and language, unspecified

F810

Specific reading disorder

F812

Mathematics disorder

F840

Autistic disorder

F842

Rett's syndrome

F843

Other childhood disintegrative disorder

F845

Asperger's syndrome

F848

Other pervasive developmental disorders

F849

Pervasive developmental disorder, unspecified

F900

Attention-deficit hyperactivity disorder, predominantly inattentive type

F901

Attention-deficit hyperactivity disorder, predominantly hyperactive type

F902

Attention-deficit hyperactivity disorder, combined type

F908

Attention-deficit hyperactivity disorder, other type

F909

Attention-deficit hyperactivity disorder, unspecified type

F910

Conduct disorder confined to family context

F911

Conduct disorder, childhood-onset type

F912

Conduct disorder, adolescent-onset type

F918

Other conduct disorders

F919

Conduct disorder, unspecified

F930

Separation anxiety disorder of childhood

F938

Other childhood emotional disorders

F939

Childhood emotional disorder, unspecified

F940

Selective mutism

F941

Reactive attachment disorder of childhood

F942

Disinhibited attachment disorder of childhood

F948

Other childhood disorders of social functioning

F949

Childhood disorder of social functioning, unspecified

F950

Transient tic disorder

F951

Chronic motor or vocal tic disorder

F952

Tourette's disorder

F958

Other tic disorders

F959

Tic disorder, unspecified

F980

Enuresis not due to a substance or known physiological condition

F981

Encopresis not due to a substance or known physiological condition

F9821

Rumination disorder of infancy and childhood

F9829

Other feeding disorders of infancy and early childhood

F983

Pica of infancy and childhood

F984

Stereotyped movement disorders

G002

Streptococcal meningitis

G003

Staphylococcal meningitis

G008

Other bacterial meningitis

G009

Bacterial meningitis, unspecified

G030

Nonpyogenic meningitis

G031

Chronic meningitis

G032

Benign recurrent meningitis [Mollaret]

G038

Meningitis due to other specified causes

G039

Meningitis, unspecified

G0400

Acute disseminated encephalitis and encephalomyelitis, unspecified

G0401

Postinfectious acute disseminated encephalitis and encephalomyelitis (postinfectious ADEM)

G0402

Postimmunization acute disseminated encephalitis, myelitis and encephalomyelitis

G041

Tropical spastic paraplegia

G042

Bacterial meningoencephalitis and meningomyelitis, not elsewhere classified

G0430

Acute necrotizing hemorrhagic encephalopathy, unspecified

G0431

Postinfectious acute necrotizing hemorrhagic encephalopathy

G0432

Postimmunization acute necrotizing hemorrhagic encephalopathy

G0439

Other acute necrotizing hemorrhagic encephalopathy

G0481

Other encephalitis and encephalomyelitis

G0482

Acute flaccid myelitis

G0489

Other myelitis

G0490

Encephalitis and encephalomyelitis, unspecified

G0491

Myelitis, unspecified

G053

Encephalitis and encephalomyelitis in diseases classified elsewhere

G054

Myelitis in diseases classified elsewhere

G060

Intracranial abscess and granuloma

G061

Intraspinal abscess and granuloma

G062

Extradural and subdural abscess, unspecified

G1111

Friedreich ataxia

G1119

Other early-onset cerebellar ataxia

G112

Late-onset cerebellar ataxia

G113

Cerebellar ataxia with defective DNA repair

G114

Hereditary spastic paraplegia

G115

Hypomyelination - hypogonadotropic hypogonadism - hypodontia

G116

Leukodystrophy with vanishing white matter disease

G118

Other hereditary ataxias

G119

Hereditary ataxia, unspecified

G120

Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]

G121

Other inherited spinal muscular atrophy

G1220

Motor neuron disease, unspecified

G1221

Amyotrophic lateral sclerosis

G1222

Progressive bulbar palsy

G1223

Primary lateral sclerosis

G1224

Familial motor neuron disease

G1225

Progressive spinal muscle atrophy

G1229

Other motor neuron disease

G128

Other spinal muscular atrophies and related syndromes

G129

Spinal muscular atrophy, unspecified

G130

Paraneoplastic neuromyopathy and neuropathy

G131

Other systemic atrophy primarily affecting central nervous system in neoplastic disease

G132

Systemic atrophy primarily affecting the central nervous system in myxedema

G138

Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere

G20A1

Parkinson's disease without dyskinesia, without mention of fluctuations

G20A2

Parkinson's disease without dyskinesia, with fluctuations