| PDX Collection 0670 (continued) |
| G8254 | Quadriplegia, C5-C7 incomplete |
| G830 | Diplegia of upper limbs |
| G931 | Anoxic brain damage, not elsewhere classified |
| G9340 | Encephalopathy, unspecified |
| G9341 | Metabolic encephalopathy |
| G9342 | Megalencephalic leukoencephalopathy with subcortical cysts |
| G9343 | Leukoencephalopathy with calcifications and cysts |
| G9344 | Adult-onset leukodystrophy with axonal spheroids |
| G9345 | Developmental and epileptic encephalopathy |
| G9349 | Other encephalopathy |
| G935 | Compression of brain |
| G936 | Cerebral edema |
| G9381 | Temporal sclerosis |
| G9389 | Other specified disorders of brain |
| G939 | Disorder of brain, unspecified |
| G969 | Disorder of central nervous system, unspecified |
| G980 | Neurogenic arthritis, not elsewhere classified |
| G988 | Other disorders of nervous system |
| I6783 | Posterior reversible encephalopathy syndrome |
| R532 | Functional quadriplegia |
| |
| PDX Collection 0671 |
| G041 | Tropical spastic paraplegia |
| G10 | Huntington's disease |
| G110 | Congenital nonprogressive ataxia |
| G1110 | Early-onset cerebellar ataxia, 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 |
| G210 | Malignant neuroleptic syndrome |
| G230 | Hallervorden-Spatz disease |
| G231 | Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski] |
| G232 | Striatonigral degeneration |
| G233 | Hypomyelination with atrophy of the basal ganglia and cerebellum |
| G238 | Other specified degenerative diseases of basal ganglia |
| G239 | Degenerative disease of basal ganglia, unspecified |
| G2401 | Drug induced subacute dyskinesia |
| G2402 | Drug induced acute dystonia |
| G2409 | Other drug induced dystonia |
| G241 | Genetic torsion dystonia |
| G242 | Idiopathic nonfamilial dystonia |
| G243 | Spasmodic torticollis |
| G244 | Idiopathic orofacial dystonia |
| G245 | Blepharospasm |
| G248 | Other dystonia |
| G249 | Dystonia, unspecified |
| G250 | Essential tremor |
| G251 | Drug-induced tremor |
| G252 | Other specified forms of tremor |
| G253 | Myoclonus |
| G254 | Drug-induced chorea |
| G255 | Other chorea |
| G2561 | Drug induced tics |
| G2569 | Other tics of organic origin |
| G2570 | Drug induced movement disorder, unspecified |
| G2571 | Drug induced akathisia |
| G2579 | Other drug induced movement disorders |
| G2582 | Stiff-man syndrome |
| G2583 | Benign shuddering attacks |
| G2589 | Other specified extrapyramidal and movement disorders |
| G259 | Extrapyramidal and movement disorder, unspecified |
| G35 | Multiple sclerosis |
| G360 | Neuromyelitis optica [Devic] |
| G361 | Acute and subacute hemorrhagic leukoencephalitis [Hurst] |
| G368 | Other specified acute disseminated demyelination |
| G369 | Acute disseminated demyelination, unspecified |
| G370 | Diffuse sclerosis of central nervous system |
| G371 | Central demyelination of corpus callosum |
| G372 | Central pontine myelinolysis |
| G373 | Acute transverse myelitis in demyelinating disease of central nervous system |
| G375 | Concentric sclerosis [Balo] of central nervous system |
| G3781 | Myelin oligodendrocyte glycoprotein antibody disease |
| G3789 | Other specified demyelinating diseases of central nervous system |
| G379 | Demyelinating disease of central nervous system, unspecified |
| G800 | Spastic quadriplegic cerebral palsy |
| G801 | Spastic diplegic cerebral palsy |
| G802 | Spastic hemiplegic cerebral palsy |
| G803 | Athetoid cerebral palsy |
| G804 | Ataxic cerebral palsy |
| G808 | Other cerebral palsy |
| G809 | Cerebral palsy, unspecified |
| G8100 | Flaccid hemiplegia affecting unspecified side |
| G8101 | Flaccid hemiplegia affecting right dominant side |
| G8102 | Flaccid hemiplegia affecting left dominant side |
| G8103 | Flaccid hemiplegia affecting right nondominant side |
| G8104 | Flaccid hemiplegia affecting left nondominant side |
| G8110 | Spastic hemiplegia affecting unspecified side |
| G8111 | Spastic hemiplegia affecting right dominant side |
| G8112 | Spastic hemiplegia affecting left dominant side |
| G8113 | Spastic hemiplegia affecting right nondominant side |
| G8114 | Spastic hemiplegia affecting left nondominant side |
| G8190 | Hemiplegia, unspecified affecting unspecified side |
| G8191 | Hemiplegia, unspecified affecting right dominant side |
| G8192 | Hemiplegia, unspecified affecting left dominant side |
| G8193 | Hemiplegia, unspecified affecting right nondominant side |
| G8194 | Hemiplegia, unspecified affecting left nondominant side |
| G8220 | Paraplegia, unspecified |
| G8221 | Paraplegia, complete |
| G8222 | Paraplegia, incomplete |
| G8250 | Quadriplegia, unspecified |
| G8251 | Quadriplegia, C1-C4 complete |
| G8252 | Quadriplegia, C1-C4 incomplete |
| G8253 | Quadriplegia, C5-C7 complete |
| G8254 | Quadriplegia, C5-C7 incomplete |
| G830 | Diplegia of upper limbs |
| G8310 | Monoplegia of lower limb affecting unspecified side |
| G8311 | Monoplegia of lower limb affecting right dominant side |
| G8312 | Monoplegia of lower limb affecting left dominant side |
| G8313 | Monoplegia of lower limb affecting right nondominant side |
| G8314 | Monoplegia of lower limb affecting left nondominant side |
| G8320 | Monoplegia of upper limb affecting unspecified side |
| G8321 | Monoplegia of upper limb affecting right dominant side |
| G8322 | Monoplegia of upper limb affecting left dominant side |
| G8323 | Monoplegia of upper limb affecting right nondominant side |
| G8324 | Monoplegia of upper limb affecting left nondominant side |
| G8330 | Monoplegia, unspecified affecting unspecified side |
| G8331 | Monoplegia, unspecified affecting right dominant side |
| G8332 | Monoplegia, unspecified affecting left dominant side |
| G8333 | Monoplegia, unspecified affecting right nondominant side |
| G8334 | Monoplegia, unspecified affecting left nondominant side |
| G834 | Cauda equina syndrome |
| G835 | Locked-in state |
| G8381 | Brown-Sequard syndrome |
| G8382 | Anterior cord syndrome |
| G8383 | Posterior cord syndrome |
| G8384 | Todd's paralysis (postepileptic) |
| G8389 | Other specified paralytic syndromes |
| G839 | Paralytic syndrome, unspecified |
| G9001 | Carotid sinus syncope |
| G9009 | Other idiopathic peripheral autonomic neuropathy |
| G902 | Horner's syndrome |
| G903 | Multi-system degeneration of the autonomic nervous system |
| G904 | Autonomic dysreflexia |
| G9050 | Complex regional pain syndrome I, unspecified |
| G90511 | Complex regional pain syndrome I of right upper limb |
| G90512 | Complex regional pain syndrome I of left upper limb |
| G90513 | Complex regional pain syndrome I of upper limb, bilateral |
| G90519 | Complex regional pain syndrome I of unspecified upper limb |
| G90521 | Complex regional pain syndrome I of right lower limb |
| G90522 | Complex regional pain syndrome I of left lower limb |
| G90523 | Complex regional pain syndrome I of lower limb, bilateral |
| G90529 | Complex regional pain syndrome I of unspecified lower limb |
| G9059 | Complex regional pain syndrome I of other specified site |
| G9081 | Serotonin syndrome |
| G9089 | Other disorders of autonomic nervous system |
| G909 | Disorder of the autonomic nervous system, unspecified |
| G90B | LMNB1-related autosomal dominant leukodystrophy |
| G930 | Cerebral cysts |
| G931 | Anoxic brain damage, not elsewhere classified |
| G9340 | Encephalopathy, unspecified |
| G9341 | Metabolic encephalopathy |
| G9342 | Megalencephalic leukoencephalopathy with subcortical cysts |
| G9343 | Leukoencephalopathy with calcifications and cysts |
| G9344 | Adult-onset leukodystrophy with axonal spheroids |
| G9345 | Developmental and epileptic encephalopathy |
| G9349 | Other encephalopathy |
| G9381 | Temporal sclerosis |
| G9389 | Other specified disorders of brain |
| G939 | Disorder of brain, unspecified |
| G950 | Syringomyelia and syringobulbia |
| G9511 | Acute infarction of spinal cord (embolic) (nonembolic) |
| G9519 | Other vascular myelopathies |
| G9520 | Unspecified cord compression |
| G9529 | Other cord compression |
| G9581 | Conus medullaris syndrome |
| G9589 | Other specified diseases of spinal cord |
| G959 | Disease of spinal cord, unspecified |
| G969 | Disorder of central nervous system, unspecified |
| G980 | Neurogenic arthritis, not elsewhere classified |
| G988 | Other disorders of nervous system |
| I6783 | Posterior reversible encephalopathy syndrome |
| R532 | Functional quadriplegia |
| |
| PDX Collection 0672 |
| G041 | Tropical spastic paraplegia |
| G10 | Huntington's disease |
| G110 | Congenital nonprogressive ataxia |
| G1110 | Early-onset cerebellar ataxia, 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 |
| G210 | Malignant neuroleptic syndrome |
| G230 | Hallervorden-Spatz disease |
| G231 | Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski] |
| G232 | Striatonigral degeneration |
| G233 | Hypomyelination with atrophy of the basal ganglia and cerebellum |
| G238 | Other specified degenerative diseases of basal ganglia |
| G239 | Degenerative disease of basal ganglia, unspecified |
| |
| PDX Collection 0673 |
| G041 | Tropical spastic paraplegia |
| G10 | Huntington's disease |
| G110 | Congenital nonprogressive ataxia |
| G1110 | Early-onset cerebellar ataxia, 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 |
| G210 | Malignant neuroleptic syndrome |
| G230 | Hallervorden-Spatz disease |
| G231 | Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski] |
| G232 | Striatonigral degeneration |
| G233 | Hypomyelination with atrophy of the basal ganglia and cerebellum |
| G238 | Other specified degenerative diseases of basal ganglia |
| G239 | Degenerative disease of basal ganglia, unspecified |
| G2401 | Drug induced subacute dyskinesia |
| G2402 | Drug induced acute dystonia |
| G2409 | Other drug induced dystonia |
| G241 | Genetic torsion dystonia |
| G242 | Idiopathic nonfamilial dystonia |
| G243 | Spasmodic torticollis |
| G244 | Idiopathic orofacial dystonia |
| G245 | Blepharospasm |
| G248 | Other dystonia |
| G249 | Dystonia, unspecified |
| G250 | Essential tremor |
| G251 | Drug-induced tremor |
| G252 | Other specified forms of tremor |
| G253 | Myoclonus |
| G254 | Drug-induced chorea |
| G255 | Other chorea |
| G2561 | Drug induced tics |
| G2569 | Other tics of organic origin |
| G2570 | Drug induced movement disorder, unspecified |
| G2571 | Drug induced akathisia |
| G2579 | Other drug induced movement disorders |
| G2582 | Stiff-man syndrome |
| G2583 | Benign shuddering attacks |
| G2589 | Other specified extrapyramidal and movement disorders |
| G259 | Extrapyramidal and movement disorder, unspecified |
| G35 | Multiple sclerosis |
| G360 | Neuromyelitis optica [Devic] |
| G361 | Acute and subacute hemorrhagic leukoencephalitis [Hurst] |
| G368 | Other specified acute disseminated demyelination |
| G369 | Acute disseminated demyelination, unspecified |
| G370 | Diffuse sclerosis of central nervous system |
| G371 | Central demyelination of corpus callosum |
| G372 | Central pontine myelinolysis |
| G373 | Acute transverse myelitis in demyelinating disease of central nervous system |
| G375 | Concentric sclerosis [Balo] of central nervous system |
| G3781 | Myelin oligodendrocyte glycoprotein antibody disease |
| G3789 | Other specified demyelinating diseases of central nervous system |
| G379 | Demyelinating disease of central nervous system, unspecified |
| G800 | Spastic quadriplegic cerebral palsy |
| G801 | Spastic diplegic cerebral palsy |
| G802 | Spastic hemiplegic cerebral palsy |
| G803 | Athetoid cerebral palsy |
| G804 | Ataxic cerebral palsy |
| G808 | Other cerebral palsy |
| G809 | Cerebral palsy, unspecified |
| G8100 | Flaccid hemiplegia affecting unspecified side |
| G8101 | Flaccid hemiplegia affecting right dominant side |
| G8102 | Flaccid hemiplegia affecting left dominant side |
| G8103 | Flaccid hemiplegia affecting right nondominant side |
| G8104 | Flaccid hemiplegia affecting left nondominant side |
| G8110 | Spastic hemiplegia affecting unspecified side |
| G8111 | Spastic hemiplegia affecting right dominant side |
| G8112 | Spastic hemiplegia affecting left dominant side |
| G8113 | Spastic hemiplegia affecting right nondominant side |
| G8114 | Spastic hemiplegia affecting left nondominant side |
| G8190 | Hemiplegia, unspecified affecting unspecified side |
| G8191 | Hemiplegia, unspecified affecting right dominant side |
| G8192 | Hemiplegia, unspecified affecting left dominant side |
| G8193 | Hemiplegia, unspecified affecting right nondominant side |
| G8194 | Hemiplegia, unspecified affecting left nondominant side |
| G8220 | Paraplegia, unspecified |
| G8221 | Paraplegia, complete |
| G8222 | Paraplegia, incomplete |
| G8250 | Quadriplegia, unspecified |
| G8251 | Quadriplegia, C1-C4 complete |
| G8252 | Quadriplegia, C1-C4 incomplete |
| G8253 | Quadriplegia, C5-C7 complete |
| G8254 | Quadriplegia, C5-C7 incomplete |
| G830 | Diplegia of upper limbs |
| G8310 | Monoplegia of lower limb affecting unspecified side |
| G8311 | Monoplegia of lower limb affecting right dominant side |
| G8312 | Monoplegia of lower limb affecting left dominant side |
| G8313 | Monoplegia of lower limb affecting right nondominant side |
| G8314 | Monoplegia of lower limb affecting left nondominant side |
| G8320 | Monoplegia of upper limb affecting unspecified side |
| G8321 | Monoplegia of upper limb affecting right dominant side |
| G8322 | Monoplegia of upper limb affecting left dominant side |
| G8323 | Monoplegia of upper limb affecting right nondominant side |
| G8324 | Monoplegia of upper limb affecting left nondominant side |
| G8330 | Monoplegia, unspecified affecting unspecified side |
| G8331 | Monoplegia, unspecified affecting right dominant side |
| G8332 | Monoplegia, unspecified affecting left dominant side |
| G8333 | Monoplegia, unspecified affecting right nondominant side |
| G8334 | Monoplegia, unspecified affecting left nondominant side |
| G834 | Cauda equina syndrome |
| G835 | Locked-in state |
| G8381 | Brown-Sequard syndrome |
| G8382 | Anterior cord syndrome |
| G8383 | Posterior cord syndrome |
| G8384 | Todd's paralysis (postepileptic) |
| G8389 | Other specified paralytic syndromes |
| G839 | Paralytic syndrome, unspecified |
| G9001 | Carotid sinus syncope |
| G9009 | Other idiopathic peripheral autonomic neuropathy |
| G902 | Horner's syndrome |
| G903 | Multi-system degeneration of the autonomic nervous system |
| G904 | Autonomic dysreflexia |
| G9050 | Complex regional pain syndrome I, unspecified |
| G90511 | Complex regional pain syndrome I of right upper limb |
| G90512 | Complex regional pain syndrome I of left upper limb |
| G90513 | Complex regional pain syndrome I of upper limb, bilateral |
| G90519 | Complex regional pain syndrome I of unspecified upper limb |
| G90521 | Complex regional pain syndrome I of right lower limb |
| G90522 | Complex regional pain syndrome I of left lower limb |
| G90523 | Complex regional pain syndrome I of lower limb, bilateral |
| G90529 | Complex regional pain syndrome I of unspecified lower limb |
| G9059 | Complex regional pain syndrome I of other specified site |
| G9081 | Serotonin syndrome |
| G9089 | Other disorders of autonomic nervous system |
| G909 | Disorder of the autonomic nervous system, unspecified |
| G90B | LMNB1-related autosomal dominant leukodystrophy |
| G931 | Anoxic brain damage, not elsewhere classified |
| G9340 | Encephalopathy, unspecified |
| G9341 | Metabolic encephalopathy |
| G9342 | Megalencephalic leukoencephalopathy with subcortical cysts |
| G9343 | Leukoencephalopathy with calcifications and cysts |
| G9344 | Adult-onset leukodystrophy with axonal spheroids |
| G9345 | Developmental and epileptic encephalopathy |
| G9349 | Other encephalopathy |
| G9381 | Temporal sclerosis |
| G9389 | Other specified disorders of brain |
| G939 | Disorder of brain, unspecified |
| G950 | Syringomyelia and syringobulbia |
| G9511 | Acute infarction of spinal cord (embolic) (nonembolic) |
| G9519 | Other vascular myelopathies |
| G9520 | Unspecified cord compression |
| G9529 | Other cord compression |
| G9581 | Conus medullaris syndrome |
| G9589 | Other specified diseases of spinal cord |
| G959 | Disease of spinal cord, unspecified |
| G9612 | Meningeal adhesions (cerebral) (spinal) |
| G969 | Disorder of central nervous system, unspecified |
| G971 | Other reaction to spinal and lumbar puncture |
| G980 | Neurogenic arthritis, not elsewhere classified |
| G988 | Other disorders of nervous system |
| I6783 | Posterior reversible encephalopathy syndrome |
| R532 | Functional quadriplegia |
| |
| PDX Collection 0674 |
| G041 | Tropical spastic paraplegia |
| G10 | Huntington's disease |
| G110 | Congenital nonprogressive ataxia |
| G1110 | Early-onset cerebellar ataxia, 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] |
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