PDX Collection 6895 (continued) |
E1140 | Type 2 diabetes mellitus with diabetic neuropathy, unspecified |
E1141 | Type 2 diabetes mellitus with diabetic mononeuropathy |
E1142 | Type 2 diabetes mellitus with diabetic polyneuropathy |
E1143 | Type 2 diabetes mellitus with diabetic autonomic (poly)neuropathy |
E1144 | Type 2 diabetes mellitus with diabetic amyotrophy |
E1149 | Type 2 diabetes mellitus with other diabetic neurological complication |
E11618 | Type 2 diabetes mellitus with other diabetic arthropathy |
E11620 | Type 2 diabetes mellitus with diabetic dermatitis |
E11621 | Type 2 diabetes mellitus with foot ulcer |
E11622 | Type 2 diabetes mellitus with other skin ulcer |
E11628 | Type 2 diabetes mellitus with other skin complications |
E11630 | Type 2 diabetes mellitus with periodontal disease |
E11638 | Type 2 diabetes mellitus with other oral complications |
E11649 | Type 2 diabetes mellitus with hypoglycemia without coma |
E1169 | Type 2 diabetes mellitus with other specified complication |
E118 | Type 2 diabetes mellitus with unspecified complications |
E1340 | Other specified diabetes mellitus with diabetic neuropathy, unspecified |
E1341 | Other specified diabetes mellitus with diabetic mononeuropathy |
E1342 | Other specified diabetes mellitus with diabetic polyneuropathy |
E1343 | Other specified diabetes mellitus with diabetic autonomic (poly)neuropathy |
E1344 | Other specified diabetes mellitus with diabetic amyotrophy |
E1349 | Other specified diabetes mellitus with other diabetic neurological complication |
E13618 | Other specified diabetes mellitus with other diabetic arthropathy |
E13620 | Other specified diabetes mellitus with diabetic dermatitis |
E13621 | Other specified diabetes mellitus with foot ulcer |
E13622 | Other specified diabetes mellitus with other skin ulcer |
E13628 | Other specified diabetes mellitus with other skin complications |
E13630 | Other specified diabetes mellitus with periodontal disease |
E13638 | Other specified diabetes mellitus with other oral complications |
E13649 | Other specified diabetes mellitus with hypoglycemia without coma |
E1365 | Other specified diabetes mellitus with hyperglycemia |
E1369 | Other specified diabetes mellitus with other specified complication |
E138 | Other specified diabetes mellitus with unspecified complications |
G113 | Cerebellar ataxia with defective DNA repair |
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 |
G9001 | Carotid sinus syncope |
G9009 | Other idiopathic peripheral autonomic neuropathy |
G902 | Horner's syndrome |
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 |
G908 | Other disorders of autonomic nervous system |
G909 | Disorder of the autonomic nervous system, unspecified |
G90B | LMNB1-related autosomal dominant leukodystrophy |
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 |
|
PDX Collection 6896 |
D8130 | Adenosine deaminase deficiency, unspecified |
D8131 | Severe combined immunodeficiency due to adenosine deaminase deficiency |
D8132 | Adenosine deaminase 2 deficiency |
D8139 | Other adenosine deaminase deficiency |
D815 | Purine nucleoside phosphorylase [PNP] deficiency |
D81810 | Biotinidase deficiency |
D841 | Defects in the complement system |
E7601 | Hurler's syndrome |
E7602 | Hurler-Scheie syndrome |
E7603 | Scheie's syndrome |
E761 | Mucopolysaccharidosis, type II |
E76210 | Morquio A mucopolysaccharidoses |
E76211 | Morquio B mucopolysaccharidoses |
E76219 | Morquio mucopolysaccharidoses, unspecified |
E7622 | Sanfilippo mucopolysaccharidoses |
E7629 | Other mucopolysaccharidoses |
E763 | Mucopolysaccharidosis, unspecified |
E768 | Other disorders of glucosaminoglycan metabolism |
E769 | Glucosaminoglycan metabolism disorder, unspecified |
E791 | Lesch-Nyhan syndrome |
E792 | Myoadenylate deaminase deficiency |
E7981 | Aicardi-Goutieres syndrome |
E7982 | Hereditary xanthinuria |
E7989 | Other specified disorders of purine and pyrimidine metabolism |
E799 | Disorder of purine and pyrimidine metabolism, unspecified |
E800 | Hereditary erythropoietic porphyria |
E801 | Porphyria cutanea tarda |
E8020 | Unspecified porphyria |
E8021 | Acute intermittent (hepatic) porphyria |
E8029 | Other porphyria |
E804 | Gilbert syndrome |
E805 | Crigler-Najjar syndrome |
E806 | Other disorders of bilirubin metabolism |
E807 | Disorder of bilirubin metabolism, unspecified |
E88810 | Metabolic syndrome |
|
PDX Collection 6897 |
D8130 | Adenosine deaminase deficiency, unspecified |
D8131 | Severe combined immunodeficiency due to adenosine deaminase deficiency |
D8132 | Adenosine deaminase 2 deficiency |
D8139 | Other adenosine deaminase deficiency |
D815 | Purine nucleoside phosphorylase [PNP] deficiency |
D81810 | Biotinidase deficiency |
D841 | Defects in the complement system |
E7601 | Hurler's syndrome |
E7602 | Hurler-Scheie syndrome |
E7603 | Scheie's syndrome |
E761 | Mucopolysaccharidosis, type II |
E76210 | Morquio A mucopolysaccharidoses |
E76211 | Morquio B mucopolysaccharidoses |
E76219 | Morquio mucopolysaccharidoses, unspecified |
E7622 | Sanfilippo mucopolysaccharidoses |
E7629 | Other mucopolysaccharidoses |
E763 | Mucopolysaccharidosis, unspecified |
E768 | Other disorders of glucosaminoglycan metabolism |
E769 | Glucosaminoglycan metabolism disorder, unspecified |
E791 | Lesch-Nyhan syndrome |
E792 | Myoadenylate deaminase deficiency |
E7981 | Aicardi-Goutieres syndrome |
E7982 | Hereditary xanthinuria |
E7989 | Other specified disorders of purine and pyrimidine metabolism |
E799 | Disorder of purine and pyrimidine metabolism, unspecified |
E800 | Hereditary erythropoietic porphyria |
E801 | Porphyria cutanea tarda |
E8020 | Unspecified porphyria |
E8021 | Acute intermittent (hepatic) porphyria |
E8029 | Other porphyria |
E804 | Gilbert syndrome |
E805 | Crigler-Najjar syndrome |
E806 | Other disorders of bilirubin metabolism |
E807 | Disorder of bilirubin metabolism, unspecified |
E88810 | Metabolic syndrome |
|
PDX Collection 6898 |
E0940 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic neuropathy, unspecified |
E0941 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic mononeuropathy |
E0942 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic polyneuropathy |
E0943 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic autonomic (poly)neuropathy |
E0944 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic amyotrophy |
E0949 | Drug or chemical induced diabetes mellitus with neurological complications with other diabetic neurological complication |
E1040 | Type 1 diabetes mellitus with diabetic neuropathy, unspecified |
E1041 | Type 1 diabetes mellitus with diabetic mononeuropathy |
E1042 | Type 1 diabetes mellitus with diabetic polyneuropathy |
E1043 | Type 1 diabetes mellitus with diabetic autonomic (poly)neuropathy |
E1044 | Type 1 diabetes mellitus with diabetic amyotrophy |
E1049 | Type 1 diabetes mellitus with other diabetic neurological complication |
E1140 | Type 2 diabetes mellitus with diabetic neuropathy, unspecified |
E1141 | Type 2 diabetes mellitus with diabetic mononeuropathy |
E1142 | Type 2 diabetes mellitus with diabetic polyneuropathy |
E1143 | Type 2 diabetes mellitus with diabetic autonomic (poly)neuropathy |
E1144 | Type 2 diabetes mellitus with diabetic amyotrophy |
E1149 | Type 2 diabetes mellitus with other diabetic neurological complication |
E1340 | Other specified diabetes mellitus with diabetic neuropathy, unspecified |
E1341 | Other specified diabetes mellitus with diabetic mononeuropathy |
E1342 | Other specified diabetes mellitus with diabetic polyneuropathy |
E1343 | Other specified diabetes mellitus with diabetic autonomic (poly)neuropathy |
E1344 | Other specified diabetes mellitus with diabetic amyotrophy |
E1349 | Other specified diabetes mellitus with other diabetic neurological complication |
G041 | Tropical spastic paraplegia |
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 |
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 |
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 |
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 |
G908 | 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 | Megaloencephalic leukoencephalopathy with subcortical cysts |
G9343 | Leukoencephalopathy with calcifications and cysts |
G9344 | Adult-onset leukodystrophy with axonal spheroids |
G9349 | Other encephalopathy |
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) |
G96191 | Perineural cyst |
G96198 | Other disorders of meninges, not elsewhere classified |
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 6899 |
E0940 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic neuropathy, unspecified |
E0941 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic mononeuropathy |
E0942 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic polyneuropathy |
E0943 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic autonomic (poly)neuropathy |
E0944 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic amyotrophy |
E0949 | Drug or chemical induced diabetes mellitus with neurological complications with other diabetic neurological complication |
E1040 | Type 1 diabetes mellitus with diabetic neuropathy, unspecified |
E1041 | Type 1 diabetes mellitus with diabetic mononeuropathy |
E1042 | Type 1 diabetes mellitus with diabetic polyneuropathy |
E1043 | Type 1 diabetes mellitus with diabetic autonomic (poly)neuropathy |
E1044 | Type 1 diabetes mellitus with diabetic amyotrophy |
E1049 | Type 1 diabetes mellitus with other diabetic neurological complication |
E1140 | Type 2 diabetes mellitus with diabetic neuropathy, unspecified |
E1141 | Type 2 diabetes mellitus with diabetic mononeuropathy |
E1142 | Type 2 diabetes mellitus with diabetic polyneuropathy |
E1143 | Type 2 diabetes mellitus with diabetic autonomic (poly)neuropathy |
E1144 | Type 2 diabetes mellitus with diabetic amyotrophy |
E1149 | Type 2 diabetes mellitus with other diabetic neurological complication |
E1340 | Other specified diabetes mellitus with diabetic neuropathy, unspecified |
E1341 | Other specified diabetes mellitus with diabetic mononeuropathy |
E1342 | Other specified diabetes mellitus with diabetic polyneuropathy |
E1343 | Other specified diabetes mellitus with diabetic autonomic (poly)neuropathy |
E1344 | Other specified diabetes mellitus with diabetic amyotrophy |
E1349 | Other specified diabetes mellitus with other diabetic neurological complication |
G041 | Tropical spastic paraplegia |
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 |
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 |
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 |