ICD-10-CM/PCS MS-DRG v38.0 R1 Definitions Manual

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Appendix C: Principal diagnoses which convert CC/MCC to non-CC
Page 352 of 454
PDX Collection 3674 (continued)
E7142Carnitine deficiency due to inborn errors of metabolism
E7143Iatrogenic carnitine deficiency
E71440Ruvalcaba-Myhre-Smith syndrome
E71448Other secondary carnitine deficiency
E71542Other group 3 peroxisomal disorders
E803Defects of catalase and peroxidase
E804Gilbert syndrome
E805Crigler-Najjar syndrome
E806Other disorders of bilirubin metabolism
E807Disorder of bilirubin metabolism, unspecified
E8840Mitochondrial metabolism disorder, unspecified
E8841MELAS syndrome
E8842MERRF syndrome
E8849Other mitochondrial metabolism disorders
E8889Other specified metabolic disorders
H49811Kearns-Sayre syndrome, right eye
H49812Kearns-Sayre syndrome, left eye
H49813Kearns-Sayre syndrome, bilateral
H49819Kearns-Sayre syndrome, unspecified eye
 
PDX Collection 3676
C965Multifocal and unisystemic Langerhans-cell histiocytosis
C966Unifocal Langerhans-cell histiocytosis
E71310Long chain/very long chain acyl CoA dehydrogenase deficiency
E71311Medium chain acyl CoA dehydrogenase deficiency
E71312Short chain acyl CoA dehydrogenase deficiency
E71313Glutaric aciduria type II
E71314Muscle carnitine palmitoyltransferase deficiency
E71318Other disorders of fatty-acid oxidation
E7132Disorders of ketone metabolism
E7139Other disorders of fatty-acid metabolism
E7140Disorder of carnitine metabolism, unspecified
E7141Primary carnitine deficiency
E7142Carnitine deficiency due to inborn errors of metabolism
E7143Iatrogenic carnitine deficiency
E71440Ruvalcaba-Myhre-Smith syndrome
E71448Other secondary carnitine deficiency
E7150Peroxisomal disorder, unspecified
E71510Zellweger syndrome
E71511Neonatal adrenoleukodystrophy
E71518Other disorders of peroxisome biogenesis
E71520Childhood cerebral X-linked adrenoleukodystrophy
E71521Adolescent X-linked adrenoleukodystrophy
E71522Adrenomyeloneuropathy
E71528Other X-linked adrenoleukodystrophy
E71529X-linked adrenoleukodystrophy, unspecified type
E7153Other group 2 peroxisomal disorders
E71540Rhizomelic chondrodysplasia punctata
E71541Zellweger-like syndrome
E71542Other group 3 peroxisomal disorders
E71548Other peroxisomal disorders
E803Defects of catalase and peroxidase
E804Gilbert syndrome
E805Crigler-Najjar syndrome
E806Other disorders of bilirubin metabolism
E807Disorder of bilirubin metabolism, unspecified
E8840Mitochondrial metabolism disorder, unspecified
E8889Other specified metabolic disorders
 
PDX Collection 3678
C965Multifocal and unisystemic Langerhans-cell histiocytosis
C966Unifocal Langerhans-cell histiocytosis
E71310Long chain/very long chain acyl CoA dehydrogenase deficiency
E71311Medium chain acyl CoA dehydrogenase deficiency
E71312Short chain acyl CoA dehydrogenase deficiency
E71313Glutaric aciduria type II
E71314Muscle carnitine palmitoyltransferase deficiency
E71318Other disorders of fatty-acid oxidation
E7132Disorders of ketone metabolism
E7139Other disorders of fatty-acid metabolism
E7140Disorder of carnitine metabolism, unspecified
E7141Primary carnitine deficiency
E7142Carnitine deficiency due to inborn errors of metabolism
E7143Iatrogenic carnitine deficiency
E71440Ruvalcaba-Myhre-Smith syndrome
E71448Other secondary carnitine deficiency
E7150Peroxisomal disorder, unspecified
E71510Zellweger syndrome
E71511Neonatal adrenoleukodystrophy
E71518Other disorders of peroxisome biogenesis
E71520Childhood cerebral X-linked adrenoleukodystrophy
E71521Adolescent X-linked adrenoleukodystrophy
E71522Adrenomyeloneuropathy
E71528Other X-linked adrenoleukodystrophy
E71529X-linked adrenoleukodystrophy, unspecified type
E7153Other group 2 peroxisomal disorders
E71540Rhizomelic chondrodysplasia punctata
E71541Zellweger-like syndrome
E71542Other group 3 peroxisomal disorders
E71548Other peroxisomal disorders
E803Defects of catalase and peroxidase
E804Gilbert syndrome
E805Crigler-Najjar syndrome
E806Other disorders of bilirubin metabolism
E807Disorder of bilirubin metabolism, unspecified
E8841MELAS syndrome
E8889Other specified metabolic disorders
 
PDX Collection 3680
C965Multifocal and unisystemic Langerhans-cell histiocytosis
C966Unifocal Langerhans-cell histiocytosis
E71310Long chain/very long chain acyl CoA dehydrogenase deficiency
E71311Medium chain acyl CoA dehydrogenase deficiency
E71312Short chain acyl CoA dehydrogenase deficiency
E71313Glutaric aciduria type II
E71314Muscle carnitine palmitoyltransferase deficiency
E71318Other disorders of fatty-acid oxidation
E7132Disorders of ketone metabolism
E7139Other disorders of fatty-acid metabolism
E7140Disorder of carnitine metabolism, unspecified
E7141Primary carnitine deficiency
E7142Carnitine deficiency due to inborn errors of metabolism
E7143Iatrogenic carnitine deficiency
E71440Ruvalcaba-Myhre-Smith syndrome
E71448Other secondary carnitine deficiency
E7150Peroxisomal disorder, unspecified
E71510Zellweger syndrome
E71511Neonatal adrenoleukodystrophy
E71518Other disorders of peroxisome biogenesis
E71520Childhood cerebral X-linked adrenoleukodystrophy
E71521Adolescent X-linked adrenoleukodystrophy
E71522Adrenomyeloneuropathy
E71528Other X-linked adrenoleukodystrophy
E71529X-linked adrenoleukodystrophy, unspecified type
E7153Other group 2 peroxisomal disorders
E71540Rhizomelic chondrodysplasia punctata
E71541Zellweger-like syndrome
E71542Other group 3 peroxisomal disorders
E71548Other peroxisomal disorders
E803Defects of catalase and peroxidase
E804Gilbert syndrome
E805Crigler-Najjar syndrome
E806Other disorders of bilirubin metabolism
E807Disorder of bilirubin metabolism, unspecified
E8842MERRF syndrome
E8889Other specified metabolic disorders
 
PDX Collection 3682
C965Multifocal and unisystemic Langerhans-cell histiocytosis
C966Unifocal Langerhans-cell histiocytosis
E71310Long chain/very long chain acyl CoA dehydrogenase deficiency
E71311Medium chain acyl CoA dehydrogenase deficiency
E71312Short chain acyl CoA dehydrogenase deficiency
E71313Glutaric aciduria type II
E71314Muscle carnitine palmitoyltransferase deficiency
E71318Other disorders of fatty-acid oxidation
E7132Disorders of ketone metabolism
E7139Other disorders of fatty-acid metabolism
E7140Disorder of carnitine metabolism, unspecified
E7141Primary carnitine deficiency
E7142Carnitine deficiency due to inborn errors of metabolism
E7143Iatrogenic carnitine deficiency
E71440Ruvalcaba-Myhre-Smith syndrome
E71448Other secondary carnitine deficiency
E7150Peroxisomal disorder, unspecified
E71510Zellweger syndrome
E71511Neonatal adrenoleukodystrophy
E71518Other disorders of peroxisome biogenesis
E71520Childhood cerebral X-linked adrenoleukodystrophy
E71521Adolescent X-linked adrenoleukodystrophy
E71522Adrenomyeloneuropathy
E71528Other X-linked adrenoleukodystrophy
E71529X-linked adrenoleukodystrophy, unspecified type
E7153Other group 2 peroxisomal disorders
E71540Rhizomelic chondrodysplasia punctata
E71541Zellweger-like syndrome
E71542Other group 3 peroxisomal disorders
E71548Other peroxisomal disorders
E803Defects of catalase and peroxidase
E804Gilbert syndrome
E805Crigler-Najjar syndrome
E806Other disorders of bilirubin metabolism
E807Disorder of bilirubin metabolism, unspecified
E8849Other mitochondrial metabolism disorders
E8889Other specified metabolic disorders
 
PDX Collection 3685
G20Parkinson's disease
G2111Neuroleptic induced parkinsonism
G2119Other drug induced secondary parkinsonism
G212Secondary parkinsonism due to other external agents
G213Postencephalitic parkinsonism
G214Vascular parkinsonism
G218Other secondary parkinsonism
G219Secondary parkinsonism, unspecified
G230Hallervorden-Spatz disease
G9001Carotid sinus syncope
G9009Other idiopathic peripheral autonomic neuropathy
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9349Other encephalopathy
I6783Posterior reversible encephalopathy syndrome
 
PDX Collection 3687
G20Parkinson's disease
G2111Neuroleptic induced parkinsonism
G2119Other drug induced secondary parkinsonism
G212Secondary parkinsonism due to other external agents
G213Postencephalitic parkinsonism
G214Vascular parkinsonism
G218Other secondary parkinsonism
G219Secondary parkinsonism, unspecified
G231Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski]
G9001Carotid sinus syncope
G9009Other idiopathic peripheral autonomic neuropathy
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9349Other encephalopathy
I6783Posterior reversible encephalopathy syndrome
 
PDX Collection 3689
G20Parkinson's disease
G2111Neuroleptic induced parkinsonism
G2119Other drug induced secondary parkinsonism
G212Secondary parkinsonism due to other external agents
G213Postencephalitic parkinsonism
G214Vascular parkinsonism
G218Other secondary parkinsonism
G219Secondary parkinsonism, unspecified
G232Striatonigral degeneration
G9001Carotid sinus syncope
G9009Other idiopathic peripheral autonomic neuropathy
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9349Other encephalopathy
I6783Posterior reversible encephalopathy syndrome
 
PDX Collection 3691
G20Parkinson's disease
G2111Neuroleptic induced parkinsonism
G2119Other drug induced secondary parkinsonism
G212Secondary parkinsonism due to other external agents
G213Postencephalitic parkinsonism
G214Vascular parkinsonism
G218Other secondary parkinsonism
G219Secondary parkinsonism, unspecified
G238Other specified degenerative diseases of basal ganglia
G9001Carotid sinus syncope
G9009Other idiopathic peripheral autonomic neuropathy
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9349Other encephalopathy
I6783Posterior reversible encephalopathy syndrome
 
PDX Collection 3693
G20Parkinson's disease
G2111Neuroleptic induced parkinsonism
G2119Other drug induced secondary parkinsonism
G212Secondary parkinsonism due to other external agents
G213Postencephalitic parkinsonism
G214Vascular parkinsonism
G218Other secondary parkinsonism
G219Secondary parkinsonism, unspecified
G239Degenerative disease of basal ganglia, unspecified
G9001Carotid sinus syncope
G9009Other idiopathic peripheral autonomic neuropathy
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9349Other encephalopathy
I6783Posterior reversible encephalopathy syndrome
 
PDX Collection 3695
G20Parkinson's disease
G2111Neuroleptic induced parkinsonism
G2119Other drug induced secondary parkinsonism
G212Secondary parkinsonism due to other external agents
G213Postencephalitic parkinsonism
G214Vascular parkinsonism
G218Other secondary parkinsonism
G219Secondary parkinsonism, unspecified
G2402Drug induced acute dystonia
G2570Drug induced movement disorder, unspecified
G2571Drug induced akathisia
G2579Other drug induced movement disorders
G2589Other specified extrapyramidal and movement disorders
G259Extrapyramidal and movement disorder, unspecified
G26Extrapyramidal and movement disorders in diseases classified elsewhere
G803Athetoid cerebral palsy
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9349Other encephalopathy
I6783Posterior reversible encephalopathy syndrome
 
PDX Collection 3697
G20Parkinson's disease
G2111Neuroleptic induced parkinsonism
G2119Other drug induced secondary parkinsonism
G212Secondary parkinsonism due to other external agents
G213Postencephalitic parkinsonism
G214Vascular parkinsonism
G218Other secondary parkinsonism
G219Secondary parkinsonism, unspecified
G2409Other drug induced dystonia
G2570Drug induced movement disorder, unspecified
G2571Drug induced akathisia
G2579Other drug induced movement disorders
G2589Other specified extrapyramidal and movement disorders
G259Extrapyramidal and movement disorder, unspecified
G26Extrapyramidal and movement disorders in diseases classified elsewhere
G803Athetoid cerebral palsy
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9349Other encephalopathy
I6783Posterior reversible encephalopathy syndrome
 
PDX Collection 3699
G20Parkinson's disease
G2111Neuroleptic induced parkinsonism
G2119Other drug induced secondary parkinsonism
G212Secondary parkinsonism due to other external agents
G213Postencephalitic parkinsonism
G214Vascular parkinsonism
G218Other secondary parkinsonism
G219Secondary parkinsonism, unspecified
G242Idiopathic nonfamilial dystonia
G2570Drug induced movement disorder, unspecified
G2571Drug induced akathisia
G2579Other drug induced movement disorders
G2589Other specified extrapyramidal and movement disorders
G259Extrapyramidal and movement disorder, unspecified
G26Extrapyramidal and movement disorders in diseases classified elsewhere
G803Athetoid cerebral palsy
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9349Other encephalopathy
I6783Posterior reversible encephalopathy syndrome
 
PDX Collection 3702
A9230West Nile virus infection, unspecified
A9231West Nile virus infection with encephalitis
A9232West Nile virus infection with other neurologic manifestation
A9239West Nile virus infection with other complications
B9721SARS-associated coronavirus as the cause of diseases classified elsewhere
G370Diffuse sclerosis of central nervous system
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9349Other encephalopathy
I6783Posterior reversible encephalopathy syndrome
 
PDX Collection 3704
G210Malignant neuroleptic syndrome
G835Locked-in state
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9349Other encephalopathy
 
PDX Collection 3706
C965Multifocal and unisystemic Langerhans-cell histiocytosis
C966Unifocal Langerhans-cell histiocytosis
E71310Long chain/very long chain acyl CoA dehydrogenase deficiency
E71311Medium chain acyl CoA dehydrogenase deficiency
E71312Short chain acyl CoA dehydrogenase deficiency
E71313Glutaric aciduria type II
E71314Muscle carnitine palmitoyltransferase deficiency
E71318Other disorders of fatty-acid oxidation
E7132Disorders of ketone metabolism
E7139Other disorders of fatty-acid metabolism
E7140Disorder of carnitine metabolism, unspecified
E7141Primary carnitine deficiency
E7142Carnitine deficiency due to inborn errors of metabolism
E7143Iatrogenic carnitine deficiency
E71440Ruvalcaba-Myhre-Smith syndrome
E71448Other secondary carnitine deficiency
E7150Peroxisomal disorder, unspecified
E71510Zellweger syndrome
E71511Neonatal adrenoleukodystrophy
E71518Other disorders of peroxisome biogenesis
E71520Childhood cerebral X-linked adrenoleukodystrophy
E71521Adolescent X-linked adrenoleukodystrophy
E71522Adrenomyeloneuropathy
E71528Other X-linked adrenoleukodystrophy
E71529X-linked adrenoleukodystrophy, unspecified type
E7153Other group 2 peroxisomal disorders
E71540Rhizomelic chondrodysplasia punctata
E71541Zellweger-like syndrome
E71542Other group 3 peroxisomal disorders
E71548Other peroxisomal disorders
E803Defects of catalase and peroxidase
E804Gilbert syndrome
E805Crigler-Najjar syndrome
E806Other disorders of bilirubin metabolism
E807Disorder of bilirubin metabolism, unspecified
E8889Other specified metabolic disorders
H49811Kearns-Sayre syndrome, right eye
 
PDX Collection 3708
C965Multifocal and unisystemic Langerhans-cell histiocytosis
C966Unifocal Langerhans-cell histiocytosis
E71310Long chain/very long chain acyl CoA dehydrogenase deficiency
E71311Medium chain acyl CoA dehydrogenase deficiency
E71312Short chain acyl CoA dehydrogenase deficiency
E71313Glutaric aciduria type II
E71314Muscle carnitine palmitoyltransferase deficiency
E71318Other disorders of fatty-acid oxidation
E7132Disorders of ketone metabolism
E7139Other disorders of fatty-acid metabolism
E7140Disorder of carnitine metabolism, unspecified
E7141Primary carnitine deficiency
E7142Carnitine deficiency due to inborn errors of metabolism
E7143Iatrogenic carnitine deficiency
E71440Ruvalcaba-Myhre-Smith syndrome
E71448Other secondary carnitine deficiency
E7150Peroxisomal disorder, unspecified
E71510Zellweger syndrome
E71511Neonatal adrenoleukodystrophy
E71518Other disorders of peroxisome biogenesis
E71520Childhood cerebral X-linked adrenoleukodystrophy
E71521Adolescent X-linked adrenoleukodystrophy
E71522Adrenomyeloneuropathy
E71528Other X-linked adrenoleukodystrophy
E71529X-linked adrenoleukodystrophy, unspecified type
E7153Other group 2 peroxisomal disorders
E71540Rhizomelic chondrodysplasia punctata
E71541Zellweger-like syndrome
E71542Other group 3 peroxisomal disorders
E71548Other peroxisomal disorders
E803Defects of catalase and peroxidase
E804Gilbert syndrome
E805Crigler-Najjar syndrome
E806Other disorders of bilirubin metabolism
E807Disorder of bilirubin metabolism, unspecified
E8889Other specified metabolic disorders
H49812Kearns-Sayre syndrome, left eye
 
PDX Collection 3710
C965Multifocal and unisystemic Langerhans-cell histiocytosis
C966Unifocal Langerhans-cell histiocytosis
E71310Long chain/very long chain acyl CoA dehydrogenase deficiency
E71311Medium chain acyl CoA dehydrogenase deficiency
E71312Short chain acyl CoA dehydrogenase deficiency
E71313Glutaric aciduria type II
E71314Muscle carnitine palmitoyltransferase deficiency
E71318Other disorders of fatty-acid oxidation
E7132Disorders of ketone metabolism
E7139Other disorders of fatty-acid metabolism



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