MS-DRG 056

Principal Diagnosis - Pdx

• A52.10 Symptomatic neurosyphilis, unspecified
• A52.11 Tabes dorsalis
• A52.12 Other cerebrospinal syphilis
• A52.15 Late syphilitic neuropathy
• A52.16 Charcot's arthropathy (tabetic)
• A52.17 General paresis
• A52.19 Other symptomatic neurosyphilis
• A52.3 Neurosyphilis, unspecified
• A81.00 Creutzfeldt-Jakob disease, unspecified
• A81.01 Variant Creutzfeldt-Jakob disease
• A81.09 Other Creutzfeldt-Jakob disease
• A81.1 Subacute sclerosing panencephalitis
• A81.2 Progressive multifocal leukoencephalopathy
• A81.81 Kuru
• A81.82 Gerstmann-Straussler-Scheinker syndrome
• A81.83 Fatal familial insomnia
• A81.89 Other atypical virus infections of central nervous system
• A81.9 Atypical virus infection of central nervous system, unspecified
• E75.00 GM2 gangliosidosis, unspecified
• E75.01 Sandhoff disease
• E75.02 Tay-Sachs disease
• E75.09 Other GM2 gangliosidosis
• E75.10 Unspecified gangliosidosis
• E75.11 Mucolipidosis IV
• E75.19 Other gangliosidosis
• E75.23 Krabbe disease
• E75.25 Metachromatic leukodystrophy
• E75.26 Sulfatase deficiency
• E75.27 Pelizaeus-Merzbacher disease
• E75.28 Canavan disease
• E75.29 Other sphingolipidosis
• E75.4 Neuronal ceroid lipofuscinosis
• F07.89 Other personality and behavioral disorders due to known physiological condition
• F48.2 Pseudobulbar affect
• F84.2 Rett's syndrome
• G10 Huntington's disease
• G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
• G12.1 Other inherited spinal muscular atrophy
• G12.20 Motor neuron disease, unspecified
• G12.21 Amyotrophic lateral sclerosis
• G12.22 Progressive bulbar palsy
• G12.23 Primary lateral sclerosis
• G12.24 Familial motor neuron disease
• G12.25 Progressive spinal muscle atrophy
• G12.29 Other motor neuron disease
• G12.8 Other spinal muscular atrophies and related syndromes
• G12.9 Spinal muscular atrophy, unspecified
• G13.2 Systemic atrophy primarily affecting the central nervous system in myxedema
• G13.8 Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere
• G20.A1 Parkinson's disease without dyskinesia, without mention of fluctuations
• G20.A2 Parkinson's disease without dyskinesia, with fluctuations
• G20.B1 Parkinson's disease with dyskinesia, without mention of fluctuations
• G20.B2 Parkinson's disease with dyskinesia, with fluctuations
• G20.C Parkinsonism, unspecified
• G21.11 Neuroleptic induced parkinsonism
• G21.19 Other drug induced secondary parkinsonism
• G21.2 Secondary parkinsonism due to other external agents
• G21.3 Postencephalitic parkinsonism
• G21.4 Vascular parkinsonism
• G21.8 Other secondary parkinsonism
• G21.9 Secondary parkinsonism, unspecified
• G23.0 Hallervorden-Spatz disease
• G23.1 Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski]
• G23.2 Striatonigral degeneration
• G23.3 Hypomyelination with atrophy of the basal ganglia and cerebellum
• G23.8 Other specified degenerative diseases of basal ganglia
• G23.9 Degenerative disease of basal ganglia, unspecified
• G24.1 Genetic torsion dystonia
• G25.4 Drug-induced chorea
• G25.5 Other chorea
• G25.70 Drug induced movement disorder, unspecified
• G25.71 Drug induced akathisia
• G25.79 Other drug induced movement disorders
• G25.81 Restless legs syndrome
• G25.89 Other specified extrapyramidal and movement disorders
• G25.9 Extrapyramidal and movement disorder, unspecified
• G26 Extrapyramidal and movement disorders in diseases classified elsewhere
• G30.0 Alzheimer's disease with early onset
• G30.1 Alzheimer's disease with late onset
• G30.8 Other Alzheimer's disease
• G30.9 Alzheimer's disease, unspecified
• G31.01 Pick's disease
• G31.09 Other frontotemporal neurocognitive disorder
• G31.1 Senile degeneration of brain, not elsewhere classified
• G31.2 Degeneration of nervous system due to alcohol
• G31.80 Leukodystrophy, unspecified
• G31.81 Alpers disease
• G31.82 Leigh's disease
• G31.83 Neurocognitive disorder with Lewy bodies
• G31.84 Mild cognitive impairment of uncertain or unknown etiology
• G31.85 Corticobasal degeneration
• G31.86 Alexander disease
• G31.89 Other specified degenerative diseases of nervous system
• G31.9 Degenerative disease of nervous system, unspecified
• G70.00 Myasthenia gravis without (acute) exacerbation
• G70.01 Myasthenia gravis with (acute) exacerbation
• G70.80 Lambert-Eaton syndrome, unspecified
• G70.81 Lambert-Eaton syndrome in disease classified elsewhere
• G73.1 Lambert-Eaton syndrome in neoplastic disease
• G73.3 Myasthenic syndromes in other diseases classified elsewhere