2025 ICD-10 CM DIAGNOSIS INDEX TERMS STARTING WITH G

  • Hemophilus meningitis - G00.0
  • Pneumococcal meningitis - G00.1
  • Streptococcal meningitis - G00.2
  • Staphylococcal meningitis - G00.3
  • Other bacterial meningitis - G00.8
  • Bacterial meningitis, unspecified - G00.9
  • Nonpyogenic meningitis - G03.0
  • Chronic meningitis - G03.1
  • Benign recurrent meningitis [Mollaret] - G03.2
  • Meningitis due to other specified causes - G03.8
  • Meningitis, unspecified - G03.9
  • Acute disseminated encephalitis and encephalomyelitis (ADEM) - G04.0
  • Acute disseminated encephalitis and encephalomyelitis, unspecified - G04.00
  • Postinfectious acute disseminated encephalitis and encephalomyelitis (postinfectious ADEM) - G04.01
  • 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 and encephalomyelitis in diseases classified elsewhere - G05.3
  • Myelitis in diseases classified elsewhere - G05.4
  • Intracranial abscess and granuloma - G06.0
  • Intraspinal abscess and granuloma - G06.1
  • Extradural and subdural abscess, unspecified - G06.2
  • 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 - G11.5
  • Leukodystrophy with vanishing white matter disease - G11.6
  • Other hereditary ataxias - G11.8
  • Hereditary ataxia, unspecified - G11.9
  • 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
  • Progressive spinal muscle atrophy - G12.25
  • Other motor neuron disease - G12.29
  • Other spinal muscular atrophies and related syndromes - G12.8
  • Spinal muscular atrophy, unspecified - G12.9
  • Paraneoplastic neuromyopathy and neuropathy - G13.0
  • Other systemic atrophy primarily affecting central nervous system in neoplastic disease - G13.1
  • Systemic atrophy primarily affecting the central nervous system in myxedema - G13.2
  • Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere - G13.8
  • Parkinson's disease without dyskinesia - G20.A
  • Parkinson's disease without dyskinesia, without mention of fluctuations - G20.A1
  • Parkinson's disease without dyskinesia, with fluctuations - G20.A2
  • Parkinson's disease with dyskinesia - G20.B
  • Parkinson's disease with dyskinesia, without mention of fluctuations - G20.B1
  • Parkinson's disease with dyskinesia, with fluctuations - G20.B2
  • Parkinsonism, unspecified - G20.C
  • Malignant neuroleptic syndrome - G21.0
  • Other drug-induced secondary parkinsonism - G21.1
  • Neuroleptic induced parkinsonism - G21.11
  • Other drug induced secondary parkinsonism - G21.19
  • Secondary parkinsonism due to other external agents - G21.2
  • Postencephalitic parkinsonism - G21.3
  • Vascular parkinsonism - G21.4
  • Other secondary parkinsonism - G21.8
  • Secondary parkinsonism, unspecified - G21.9
  • Hallervorden-Spatz disease - G23.0
  • Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski] - G23.1
  • Striatonigral degeneration - G23.2
  • Hypomyelination with atrophy of the basal ganglia and cerebellum - G23.3
  • Other specified degenerative diseases of basal ganglia - G23.8
  • Degenerative disease of basal ganglia, unspecified - G23.9
  • Drug induced dystonia - G24.0
  • Drug induced subacute dyskinesia - G24.01
  • Drug induced acute dystonia - G24.02
  • Other drug induced dystonia - G24.09
  • Genetic torsion dystonia - G24.1
  • Idiopathic nonfamilial dystonia - G24.2
  • Spasmodic torticollis - G24.3
  • Idiopathic orofacial dystonia - G24.4
  • Blepharospasm - G24.5
  • Other dystonia - G24.8
  • Dystonia, unspecified - G24.9
  • Essential tremor - G25.0
  • Drug-induced tremor - G25.1
  • Other specified forms of tremor - G25.2
  • Myoclonus - G25.3
  • Drug-induced chorea - G25.4