Bloodwork

ICD-10-CM codes

The diagnosis classification on lab requisitions and clinical records. Every condition on this site is anchored to an ICD-10-CM code.

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22 chapters

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97,584 codes · page 126 of 1,952

Acute disseminated encephalitis and encephalomyelitis, unspecified G04.00 Postinfectious acute disseminated encephalitis and encephalomyelitis (postinfectious ADEM) G04.01 Postimmun ac dissem encphlts, myelitis and encephalomyelitis Postimmunization acute disseminated encephalitis, myelitis and encephalomyelitis G04.02 Tropical spastic paraplegia G04.1 Bacterial meningoencephalitis and meningomyelitis, not elsewhere classified G04.2 Acute necrotizing hemorrhagic encephalopathy G04.3 Acute necrotizing hemorrhagic encephalopathy, unspecified G04.30 Postinfectious acute necrotizing hemorrhagic encephalopathy G04.31 Postimmunization acute necrotizing hemorrhagic encephalopathy G04.32 Other acute necrotizing hemorrhagic encephalopathy G04.39 Other encephalitis, myelitis and encephalomyelitis G04.8 Other encephalitis and encephalomyelitis G04.81 Acute flaccid myelitis G04.82 Other myelitis G04.89 Encephalitis, myelitis and encephalomyelitis, unspecified G04.9 Encephalitis and encephalomyelitis, unspecified G04.90 Myelitis, unspecified G04.91 Encephalitis, myelitis and encephalomyelitis in diseases classified elsewhere G05 Encephalitis and encephalomyelitis in diseases classd elswhr Encephalitis and encephalomyelitis in diseases classified elsewhere G05.3 Myelitis in diseases classified elsewhere G05.4 Intracranial and intraspinal abscess and granuloma G06 Intracranial abscess and granuloma G06.0 Intraspinal abscess and granuloma G06.1 Extradural and subdural abscess, unspecified G06.2 Intracranial and intraspinal abscess and granuloma in diseases classified elsewhere G07 Intracranial and intraspinal phlebitis and thrombophlebitis G08 Sequelae of inflammatory diseases of central nervous system G09 Huntington's disease G10 Hereditary ataxia G11 Congenital nonprogressive ataxia G11.0 Early-onset cerebellar ataxia G11.1 Early-onset cerebellar ataxia, unspecified G11.10 Friedreich ataxia G11.11 Other early-onset cerebellar ataxia G11.19 Late-onset cerebellar ataxia G11.2 Cerebellar ataxia with defective DNA repair G11.3 Hereditary spastic paraplegia G11.4 Hypomyelination - hypogonadotropic hypogonadism - hypodontia Hypomyelination - hypogonadotropic hypogonadism - hypodontia G11.5 Leukodystrophy with vanishing white matter disease G11.6 Other hereditary ataxias G11.8 Hereditary ataxia, unspecified G11.9 Spinal muscular atrophy and related syndromes G12 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] G12.0 Other inherited spinal muscular atrophy G12.1 Motor neuron disease G12.2 Motor neuron disease, unspecified G12.20 Amyotrophic lateral sclerosis G12.21 Progressive bulbar palsy G12.22 Primary lateral sclerosis G12.23 Familial motor neuron disease G12.24