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 |