| PDX Collection 3674 (continued) |
| E7142 | Carnitine deficiency due to inborn errors of metabolism |
| E7143 | Iatrogenic carnitine deficiency |
| E71440 | Ruvalcaba-Myhre-Smith syndrome |
| E71448 | Other secondary carnitine deficiency |
| E71542 | Other group 3 peroxisomal disorders |
| E803 | Defects of catalase and peroxidase |
| E804 | Gilbert syndrome |
| E805 | Crigler-Najjar syndrome |
| E806 | Other disorders of bilirubin metabolism |
| E807 | Disorder of bilirubin metabolism, unspecified |
| E8840 | Mitochondrial metabolism disorder, unspecified |
| E8841 | MELAS syndrome |
| E8842 | MERRF syndrome |
| E8849 | Other mitochondrial metabolism disorders |
| E8889 | Other specified metabolic disorders |
| H49811 | Kearns-Sayre syndrome, right eye |
| H49812 | Kearns-Sayre syndrome, left eye |
| H49813 | Kearns-Sayre syndrome, bilateral |
| H49819 | Kearns-Sayre syndrome, unspecified eye |
| |
| PDX Collection 3676 |
| C965 | Multifocal and unisystemic Langerhans-cell histiocytosis |
| C966 | Unifocal Langerhans-cell histiocytosis |
| E71310 | Long chain/very long chain acyl CoA dehydrogenase deficiency |
| E71311 | Medium chain acyl CoA dehydrogenase deficiency |
| E71312 | Short chain acyl CoA dehydrogenase deficiency |
| E71313 | Glutaric aciduria type II |
| E71314 | Muscle carnitine palmitoyltransferase deficiency |
| E71318 | Other disorders of fatty-acid oxidation |
| E7132 | Disorders of ketone metabolism |
| E7139 | Other disorders of fatty-acid metabolism |
| E7140 | Disorder of carnitine metabolism, unspecified |
| E7141 | Primary carnitine deficiency |
| E7142 | Carnitine deficiency due to inborn errors of metabolism |
| E7143 | Iatrogenic carnitine deficiency |
| E71440 | Ruvalcaba-Myhre-Smith syndrome |
| E71448 | Other secondary carnitine deficiency |
| E7150 | Peroxisomal disorder, unspecified |
| E71510 | Zellweger syndrome |
| E71511 | Neonatal adrenoleukodystrophy |
| E71518 | Other disorders of peroxisome biogenesis |
| E71520 | Childhood cerebral X-linked adrenoleukodystrophy |
| E71521 | Adolescent X-linked adrenoleukodystrophy |
| E71522 | Adrenomyeloneuropathy |
| E71528 | Other X-linked adrenoleukodystrophy |
| E71529 | X-linked adrenoleukodystrophy, unspecified type |
| E7153 | Other group 2 peroxisomal disorders |
| E71540 | Rhizomelic chondrodysplasia punctata |
| E71541 | Zellweger-like syndrome |
| E71542 | Other group 3 peroxisomal disorders |
| E71548 | Other peroxisomal disorders |
| E803 | Defects of catalase and peroxidase |
| E804 | Gilbert syndrome |
| E805 | Crigler-Najjar syndrome |
| E806 | Other disorders of bilirubin metabolism |
| E807 | Disorder of bilirubin metabolism, unspecified |
| E8840 | Mitochondrial metabolism disorder, unspecified |
| E8889 | Other specified metabolic disorders |
| |
| PDX Collection 3678 |
| C965 | Multifocal and unisystemic Langerhans-cell histiocytosis |
| C966 | Unifocal Langerhans-cell histiocytosis |
| E71310 | Long chain/very long chain acyl CoA dehydrogenase deficiency |
| E71311 | Medium chain acyl CoA dehydrogenase deficiency |
| E71312 | Short chain acyl CoA dehydrogenase deficiency |
| E71313 | Glutaric aciduria type II |
| E71314 | Muscle carnitine palmitoyltransferase deficiency |
| E71318 | Other disorders of fatty-acid oxidation |
| E7132 | Disorders of ketone metabolism |
| E7139 | Other disorders of fatty-acid metabolism |
| E7140 | Disorder of carnitine metabolism, unspecified |
| E7141 | Primary carnitine deficiency |
| E7142 | Carnitine deficiency due to inborn errors of metabolism |
| E7143 | Iatrogenic carnitine deficiency |
| E71440 | Ruvalcaba-Myhre-Smith syndrome |
| E71448 | Other secondary carnitine deficiency |
| E7150 | Peroxisomal disorder, unspecified |
| E71510 | Zellweger syndrome |
| E71511 | Neonatal adrenoleukodystrophy |
| E71518 | Other disorders of peroxisome biogenesis |
| E71520 | Childhood cerebral X-linked adrenoleukodystrophy |
| E71521 | Adolescent X-linked adrenoleukodystrophy |
| E71522 | Adrenomyeloneuropathy |
| E71528 | Other X-linked adrenoleukodystrophy |
| E71529 | X-linked adrenoleukodystrophy, unspecified type |
| E7153 | Other group 2 peroxisomal disorders |
| E71540 | Rhizomelic chondrodysplasia punctata |
| E71541 | Zellweger-like syndrome |
| E71542 | Other group 3 peroxisomal disorders |
| E71548 | Other peroxisomal disorders |
| E803 | Defects of catalase and peroxidase |
| E804 | Gilbert syndrome |
| E805 | Crigler-Najjar syndrome |
| E806 | Other disorders of bilirubin metabolism |
| E807 | Disorder of bilirubin metabolism, unspecified |
| E8841 | MELAS syndrome |
| E8889 | Other specified metabolic disorders |
| |
| PDX Collection 3680 |
| C965 | Multifocal and unisystemic Langerhans-cell histiocytosis |
| C966 | Unifocal Langerhans-cell histiocytosis |
| E71310 | Long chain/very long chain acyl CoA dehydrogenase deficiency |
| E71311 | Medium chain acyl CoA dehydrogenase deficiency |
| E71312 | Short chain acyl CoA dehydrogenase deficiency |
| E71313 | Glutaric aciduria type II |
| E71314 | Muscle carnitine palmitoyltransferase deficiency |
| E71318 | Other disorders of fatty-acid oxidation |
| E7132 | Disorders of ketone metabolism |
| E7139 | Other disorders of fatty-acid metabolism |
| E7140 | Disorder of carnitine metabolism, unspecified |
| E7141 | Primary carnitine deficiency |
| E7142 | Carnitine deficiency due to inborn errors of metabolism |
| E7143 | Iatrogenic carnitine deficiency |
| E71440 | Ruvalcaba-Myhre-Smith syndrome |
| E71448 | Other secondary carnitine deficiency |
| E7150 | Peroxisomal disorder, unspecified |
| E71510 | Zellweger syndrome |
| E71511 | Neonatal adrenoleukodystrophy |
| E71518 | Other disorders of peroxisome biogenesis |
| E71520 | Childhood cerebral X-linked adrenoleukodystrophy |
| E71521 | Adolescent X-linked adrenoleukodystrophy |
| E71522 | Adrenomyeloneuropathy |
| E71528 | Other X-linked adrenoleukodystrophy |
| E71529 | X-linked adrenoleukodystrophy, unspecified type |
| E7153 | Other group 2 peroxisomal disorders |
| E71540 | Rhizomelic chondrodysplasia punctata |
| E71541 | Zellweger-like syndrome |
| E71542 | Other group 3 peroxisomal disorders |
| E71548 | Other peroxisomal disorders |
| E803 | Defects of catalase and peroxidase |
| E804 | Gilbert syndrome |
| E805 | Crigler-Najjar syndrome |
| E806 | Other disorders of bilirubin metabolism |
| E807 | Disorder of bilirubin metabolism, unspecified |
| E8842 | MERRF syndrome |
| E8889 | Other specified metabolic disorders |
| |
| PDX Collection 3682 |
| C965 | Multifocal and unisystemic Langerhans-cell histiocytosis |
| C966 | Unifocal Langerhans-cell histiocytosis |
| E71310 | Long chain/very long chain acyl CoA dehydrogenase deficiency |
| E71311 | Medium chain acyl CoA dehydrogenase deficiency |
| E71312 | Short chain acyl CoA dehydrogenase deficiency |
| E71313 | Glutaric aciduria type II |
| E71314 | Muscle carnitine palmitoyltransferase deficiency |
| E71318 | Other disorders of fatty-acid oxidation |
| E7132 | Disorders of ketone metabolism |
| E7139 | Other disorders of fatty-acid metabolism |
| E7140 | Disorder of carnitine metabolism, unspecified |
| E7141 | Primary carnitine deficiency |
| E7142 | Carnitine deficiency due to inborn errors of metabolism |
| E7143 | Iatrogenic carnitine deficiency |
| E71440 | Ruvalcaba-Myhre-Smith syndrome |
| E71448 | Other secondary carnitine deficiency |
| E7150 | Peroxisomal disorder, unspecified |
| E71510 | Zellweger syndrome |
| E71511 | Neonatal adrenoleukodystrophy |
| E71518 | Other disorders of peroxisome biogenesis |
| E71520 | Childhood cerebral X-linked adrenoleukodystrophy |
| E71521 | Adolescent X-linked adrenoleukodystrophy |
| E71522 | Adrenomyeloneuropathy |
| E71528 | Other X-linked adrenoleukodystrophy |
| E71529 | X-linked adrenoleukodystrophy, unspecified type |
| E7153 | Other group 2 peroxisomal disorders |
| E71540 | Rhizomelic chondrodysplasia punctata |
| E71541 | Zellweger-like syndrome |
| E71542 | Other group 3 peroxisomal disorders |
| E71548 | Other peroxisomal disorders |
| E803 | Defects of catalase and peroxidase |
| E804 | Gilbert syndrome |
| E805 | Crigler-Najjar syndrome |
| E806 | Other disorders of bilirubin metabolism |
| E807 | Disorder of bilirubin metabolism, unspecified |
| E8849 | Other mitochondrial metabolism disorders |
| E8889 | Other specified metabolic disorders |
| |
| PDX Collection 3685 |
| G20 | Parkinson's disease |
| G2111 | Neuroleptic induced parkinsonism |
| G2119 | Other drug induced secondary parkinsonism |
| G212 | Secondary parkinsonism due to other external agents |
| G213 | Postencephalitic parkinsonism |
| G214 | Vascular parkinsonism |
| G218 | Other secondary parkinsonism |
| G219 | Secondary parkinsonism, unspecified |
| G230 | Hallervorden-Spatz disease |
| G9001 | Carotid sinus syncope |
| G9009 | Other idiopathic peripheral autonomic neuropathy |
| G9340 | Encephalopathy, unspecified |
| G9341 | Metabolic encephalopathy |
| G9349 | Other encephalopathy |
| I6783 | Posterior reversible encephalopathy syndrome |
| |
| PDX Collection 3687 |
| G20 | Parkinson's disease |
| G2111 | Neuroleptic induced parkinsonism |
| G2119 | Other drug induced secondary parkinsonism |
| G212 | Secondary parkinsonism due to other external agents |
| G213 | Postencephalitic parkinsonism |
| G214 | Vascular parkinsonism |
| G218 | Other secondary parkinsonism |
| G219 | Secondary parkinsonism, unspecified |
| G231 | Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski] |
| G9001 | Carotid sinus syncope |
| G9009 | Other idiopathic peripheral autonomic neuropathy |
| G9340 | Encephalopathy, unspecified |
| G9341 | Metabolic encephalopathy |
| G9349 | Other encephalopathy |
| I6783 | Posterior reversible encephalopathy syndrome |
| |
| PDX Collection 3689 |
| G20 | Parkinson's disease |
| G2111 | Neuroleptic induced parkinsonism |
| G2119 | Other drug induced secondary parkinsonism |
| G212 | Secondary parkinsonism due to other external agents |
| G213 | Postencephalitic parkinsonism |
| G214 | Vascular parkinsonism |
| G218 | Other secondary parkinsonism |
| G219 | Secondary parkinsonism, unspecified |
| G232 | Striatonigral degeneration |
| G9001 | Carotid sinus syncope |
| G9009 | Other idiopathic peripheral autonomic neuropathy |
| G9340 | Encephalopathy, unspecified |
| G9341 | Metabolic encephalopathy |
| G9349 | Other encephalopathy |
| I6783 | Posterior reversible encephalopathy syndrome |
| |
| PDX Collection 3691 |
| G20 | Parkinson's disease |
| G2111 | Neuroleptic induced parkinsonism |
| G2119 | Other drug induced secondary parkinsonism |
| G212 | Secondary parkinsonism due to other external agents |
| G213 | Postencephalitic parkinsonism |
| G214 | Vascular parkinsonism |
| G218 | Other secondary parkinsonism |
| G219 | Secondary parkinsonism, unspecified |
| G238 | Other specified degenerative diseases of basal ganglia |
| G9001 | Carotid sinus syncope |
| G9009 | Other idiopathic peripheral autonomic neuropathy |
| G9340 | Encephalopathy, unspecified |
| G9341 | Metabolic encephalopathy |
| G9349 | Other encephalopathy |
| I6783 | Posterior reversible encephalopathy syndrome |
| |
| PDX Collection 3693 |
| G20 | Parkinson's disease |
| G2111 | Neuroleptic induced parkinsonism |
| G2119 | Other drug induced secondary parkinsonism |
| G212 | Secondary parkinsonism due to other external agents |
| G213 | Postencephalitic parkinsonism |
| G214 | Vascular parkinsonism |
| G218 | Other secondary parkinsonism |
| G219 | Secondary parkinsonism, unspecified |
| G239 | Degenerative disease of basal ganglia, unspecified |
| G9001 | Carotid sinus syncope |
| G9009 | Other idiopathic peripheral autonomic neuropathy |
| G9340 | Encephalopathy, unspecified |
| G9341 | Metabolic encephalopathy |
| G9349 | Other encephalopathy |
| I6783 | Posterior reversible encephalopathy syndrome |
| |
| PDX Collection 3695 |
| G20 | Parkinson's disease |
| G2111 | Neuroleptic induced parkinsonism |
| G2119 | Other drug induced secondary parkinsonism |
| G212 | Secondary parkinsonism due to other external agents |
| G213 | Postencephalitic parkinsonism |
| G214 | Vascular parkinsonism |
| G218 | Other secondary parkinsonism |
| G219 | Secondary parkinsonism, unspecified |
| G2402 | Drug induced acute dystonia |
| G2570 | Drug induced movement disorder, unspecified |
| G2571 | Drug induced akathisia |
| G2579 | Other drug induced movement disorders |
| G2589 | Other specified extrapyramidal and movement disorders |
| G259 | Extrapyramidal and movement disorder, unspecified |
| G26 | Extrapyramidal and movement disorders in diseases classified elsewhere |
| G803 | Athetoid cerebral palsy |
| G9340 | Encephalopathy, unspecified |
| G9341 | Metabolic encephalopathy |
| G9349 | Other encephalopathy |
| I6783 | Posterior reversible encephalopathy syndrome |
| |
| PDX Collection 3697 |
| G20 | Parkinson's disease |
| G2111 | Neuroleptic induced parkinsonism |
| G2119 | Other drug induced secondary parkinsonism |
| G212 | Secondary parkinsonism due to other external agents |
| G213 | Postencephalitic parkinsonism |
| G214 | Vascular parkinsonism |
| G218 | Other secondary parkinsonism |
| G219 | Secondary parkinsonism, unspecified |
| G2409 | Other drug induced dystonia |
| G2570 | Drug induced movement disorder, unspecified |
| G2571 | Drug induced akathisia |
| G2579 | Other drug induced movement disorders |
| G2589 | Other specified extrapyramidal and movement disorders |
| G259 | Extrapyramidal and movement disorder, unspecified |
| G26 | Extrapyramidal and movement disorders in diseases classified elsewhere |
| G803 | Athetoid cerebral palsy |
| G9340 | Encephalopathy, unspecified |
| G9341 | Metabolic encephalopathy |
| G9349 | Other encephalopathy |
| I6783 | Posterior reversible encephalopathy syndrome |
| |
| PDX Collection 3699 |
| G20 | Parkinson's disease |
| G2111 | Neuroleptic induced parkinsonism |
| G2119 | Other drug induced secondary parkinsonism |
| G212 | Secondary parkinsonism due to other external agents |
| G213 | Postencephalitic parkinsonism |
| G214 | Vascular parkinsonism |
| G218 | Other secondary parkinsonism |
| G219 | Secondary parkinsonism, unspecified |
| G242 | Idiopathic nonfamilial dystonia |
| G2570 | Drug induced movement disorder, unspecified |
| G2571 | Drug induced akathisia |
| G2579 | Other drug induced movement disorders |
| G2589 | Other specified extrapyramidal and movement disorders |
| G259 | Extrapyramidal and movement disorder, unspecified |
| G26 | Extrapyramidal and movement disorders in diseases classified elsewhere |
| G803 | Athetoid cerebral palsy |
| G9340 | Encephalopathy, unspecified |
| G9341 | Metabolic encephalopathy |
| G9349 | Other encephalopathy |
| I6783 | Posterior reversible encephalopathy syndrome |
| |
| PDX Collection 3702 |
| A9230 | West Nile virus infection, unspecified |
| A9231 | West Nile virus infection with encephalitis |
| A9232 | West Nile virus infection with other neurologic manifestation |
| A9239 | West Nile virus infection with other complications |
| B9721 | SARS-associated coronavirus as the cause of diseases classified elsewhere |
| G370 | Diffuse sclerosis of central nervous system |
| G9340 | Encephalopathy, unspecified |
| G9341 | Metabolic encephalopathy |
| G9349 | Other encephalopathy |
| I6783 | Posterior reversible encephalopathy syndrome |
| |
| PDX Collection 3704 |
| G210 | Malignant neuroleptic syndrome |
| G835 | Locked-in state |
| G9340 | Encephalopathy, unspecified |
| G9341 | Metabolic encephalopathy |
| G9349 | Other encephalopathy |
| |
| PDX Collection 3706 |
| C965 | Multifocal and unisystemic Langerhans-cell histiocytosis |
| C966 | Unifocal Langerhans-cell histiocytosis |
| E71310 | Long chain/very long chain acyl CoA dehydrogenase deficiency |
| E71311 | Medium chain acyl CoA dehydrogenase deficiency |
| E71312 | Short chain acyl CoA dehydrogenase deficiency |
| E71313 | Glutaric aciduria type II |
| E71314 | Muscle carnitine palmitoyltransferase deficiency |
| E71318 | Other disorders of fatty-acid oxidation |
| E7132 | Disorders of ketone metabolism |
| E7139 | Other disorders of fatty-acid metabolism |
| E7140 | Disorder of carnitine metabolism, unspecified |
| E7141 | Primary carnitine deficiency |
| E7142 | Carnitine deficiency due to inborn errors of metabolism |
| E7143 | Iatrogenic carnitine deficiency |
| E71440 | Ruvalcaba-Myhre-Smith syndrome |
| E71448 | Other secondary carnitine deficiency |
| E7150 | Peroxisomal disorder, unspecified |
| E71510 | Zellweger syndrome |
| E71511 | Neonatal adrenoleukodystrophy |
| E71518 | Other disorders of peroxisome biogenesis |
| E71520 | Childhood cerebral X-linked adrenoleukodystrophy |
| E71521 | Adolescent X-linked adrenoleukodystrophy |
| E71522 | Adrenomyeloneuropathy |
| E71528 | Other X-linked adrenoleukodystrophy |
| E71529 | X-linked adrenoleukodystrophy, unspecified type |
| E7153 | Other group 2 peroxisomal disorders |
| E71540 | Rhizomelic chondrodysplasia punctata |
| E71541 | Zellweger-like syndrome |
| E71542 | Other group 3 peroxisomal disorders |
| E71548 | Other peroxisomal disorders |
| E803 | Defects of catalase and peroxidase |
| E804 | Gilbert syndrome |
| E805 | Crigler-Najjar syndrome |
| E806 | Other disorders of bilirubin metabolism |
| E807 | Disorder of bilirubin metabolism, unspecified |
| E8889 | Other specified metabolic disorders |
| H49811 | Kearns-Sayre syndrome, right eye |
| |
| PDX Collection 3708 |
| C965 | Multifocal and unisystemic Langerhans-cell histiocytosis |
| C966 | Unifocal Langerhans-cell histiocytosis |
| E71310 | Long chain/very long chain acyl CoA dehydrogenase deficiency |
| E71311 | Medium chain acyl CoA dehydrogenase deficiency |
| E71312 | Short chain acyl CoA dehydrogenase deficiency |
| E71313 | Glutaric aciduria type II |
| E71314 | Muscle carnitine palmitoyltransferase deficiency |
| E71318 | Other disorders of fatty-acid oxidation |
| E7132 | Disorders of ketone metabolism |
| E7139 | Other disorders of fatty-acid metabolism |
| E7140 | Disorder of carnitine metabolism, unspecified |
| E7141 | Primary carnitine deficiency |
| E7142 | Carnitine deficiency due to inborn errors of metabolism |
| E7143 | Iatrogenic carnitine deficiency |
| E71440 | Ruvalcaba-Myhre-Smith syndrome |
| E71448 | Other secondary carnitine deficiency |
| E7150 | Peroxisomal disorder, unspecified |
| E71510 | Zellweger syndrome |
| E71511 | Neonatal adrenoleukodystrophy |
| E71518 | Other disorders of peroxisome biogenesis |
| E71520 | Childhood cerebral X-linked adrenoleukodystrophy |
| E71521 | Adolescent X-linked adrenoleukodystrophy |
| E71522 | Adrenomyeloneuropathy |
| E71528 | Other X-linked adrenoleukodystrophy |
| E71529 | X-linked adrenoleukodystrophy, unspecified type |
| E7153 | Other group 2 peroxisomal disorders |
| E71540 | Rhizomelic chondrodysplasia punctata |
| E71541 | Zellweger-like syndrome |
| E71542 | Other group 3 peroxisomal disorders |
| E71548 | Other peroxisomal disorders |
| E803 | Defects of catalase and peroxidase |
| E804 | Gilbert syndrome |
| E805 | Crigler-Najjar syndrome |
| E806 | Other disorders of bilirubin metabolism |
| E807 | Disorder of bilirubin metabolism, unspecified |
| E8889 | Other specified metabolic disorders |
| H49812 | Kearns-Sayre syndrome, left eye |
| |
| PDX Collection 3710 |
| C965 | Multifocal and unisystemic Langerhans-cell histiocytosis |
| C966 | Unifocal Langerhans-cell histiocytosis |
| E71310 | Long chain/very long chain acyl CoA dehydrogenase deficiency |
| E71311 | Medium chain acyl CoA dehydrogenase deficiency |
| E71312 | Short chain acyl CoA dehydrogenase deficiency |
| E71313 | Glutaric aciduria type II |
| E71314 | Muscle carnitine palmitoyltransferase deficiency |
| E71318 | Other disorders of fatty-acid oxidation |
| E7132 | Disorders of ketone metabolism |
| E7139 | Other disorders of fatty-acid metabolism |
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