ICD-10-CM/PCS MS-DRG v39.0 Definitions Manual

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Appendix C: Principal diagnoses which convert CC/MCC to non-CC
Page 56 of 689
PDX Collection 0534 (continued)
E771Defects in glycoprotein degradation
E778Other disorders of glycoprotein metabolism
E779Disorder of glycoprotein metabolism, unspecified
E7800Pure hypercholesterolemia, unspecified
E7801Familial hypercholesterolemia
E781Pure hyperglyceridemia
E782Mixed hyperlipidemia
E783Hyperchylomicronemia
E7841Elevated Lipoprotein(a)
E7849Other hyperlipidemia
E785Hyperlipidemia, unspecified
E786Lipoprotein deficiency
E7870Disorder of bile acid and cholesterol metabolism, unspecified
E7879Other disorders of bile acid and cholesterol metabolism
E7881Lipoid dermatoarthritis
E7889Other lipoprotein metabolism disorders
E789Disorder of lipoprotein metabolism, unspecified
E8802Plasminogen deficiency
E8809Other disorders of plasma-protein metabolism, not elsewhere classified
E881Lipodystrophy, not elsewhere classified
E882Lipomatosis, not elsewhere classified
E8889Other specified metabolic disorders
 
PDX Collection 0535
C965Multifocal and unisystemic Langerhans-cell histiocytosis
C966Unifocal Langerhans-cell histiocytosis
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
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 0536
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
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
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 0537
E7500GM2 gangliosidosis, unspecified
E7501Sandhoff disease
E7502Tay-Sachs disease
E7509Other GM2 gangliosidosis
E7510Unspecified gangliosidosis
E7511Mucolipidosis IV
E7519Other gangliosidosis
E754Neuronal ceroid lipofuscinosis
F842Rett's syndrome
G132Systemic atrophy primarily affecting the central nervous system in myxedema
G138Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere
G300Alzheimer's disease with early onset
G301Alzheimer's disease with late onset
G308Other Alzheimer's disease
G309Alzheimer's disease, unspecified
G3101Pick's disease
G3109Other frontotemporal dementia
G311Senile degeneration of brain, not elsewhere classified
G312Degeneration of nervous system due to alcohol
G3181Alpers disease
G3182Leigh's disease
G3184Mild cognitive impairment, so stated
G3185Corticobasal degeneration
G3189Other specified degenerative diseases of nervous system
G319Degenerative disease of nervous system, unspecified
G914Hydrocephalus in diseases classified elsewhere
G94Other disorders of brain in diseases classified elsewhere
 
PDX Collection 0538
E7500GM2 gangliosidosis, unspecified
E7501Sandhoff disease
E7502Tay-Sachs disease
E7509Other GM2 gangliosidosis
E7510Unspecified gangliosidosis
E7511Mucolipidosis IV
E7519Other gangliosidosis
E7523Krabbe disease
E7525Metachromatic leukodystrophy
E7526Sulfatase deficiency
E7529Other sphingolipidosis
E754Neuronal ceroid lipofuscinosis
F842Rett's syndrome
G132Systemic atrophy primarily affecting the central nervous system in myxedema
G138Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere
G312Degeneration of nervous system due to alcohol
G3181Alpers disease
G3182Leigh's disease
G3289Other specified degenerative disorders of nervous system in diseases classified elsewhere
G914Hydrocephalus in diseases classified elsewhere
G9381Temporal sclerosis
G9389Other specified disorders of brain
G939Disorder of brain, unspecified
G94Other disorders of brain in diseases classified elsewhere
G969Disorder of central nervous system, unspecified
G980Neurogenic arthritis, not elsewhere classified
G988Other disorders of nervous system
G998Other specified disorders of nervous system in diseases classified elsewhere
 
PDX Collection 0539
D8130Adenosine deaminase deficiency, unspecified
D8131Severe combined immunodeficiency due to adenosine deaminase deficiency
D8132Adenosine deaminase 2 deficiency
D8139Other adenosine deaminase deficiency
D815Purine nucleoside phosphorylase [PNP] deficiency
D81810Biotinidase deficiency
D841Defects in the complement system
E7601Hurler's syndrome
E7602Hurler-Scheie syndrome
E7603Scheie's syndrome
E761Mucopolysaccharidosis, type II
E76210Morquio A mucopolysaccharidoses
E76211Morquio B mucopolysaccharidoses
E76219Morquio mucopolysaccharidoses, unspecified
E7622Sanfilippo mucopolysaccharidoses
E7629Other mucopolysaccharidoses
E763Mucopolysaccharidosis, unspecified
E768Other disorders of glucosaminoglycan metabolism
E769Glucosaminoglycan metabolism disorder, unspecified
E791Lesch-Nyhan syndrome
E792Myoadenylate deaminase deficiency
E798Other disorders of purine and pyrimidine metabolism
E799Disorder of purine and pyrimidine metabolism, unspecified
E800Hereditary erythropoietic porphyria
E801Porphyria cutanea tarda
E8020Unspecified porphyria
E8021Acute intermittent (hepatic) porphyria
E8029Other porphyria
E804Gilbert syndrome
E805Crigler-Najjar syndrome
E806Other disorders of bilirubin metabolism
E807Disorder of bilirubin metabolism, unspecified
E850Non-neuropathic heredofamilial amyloidosis
E859Amyloidosis, unspecified
E8881Metabolic syndrome
 
PDX Collection 0540
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
Q872Congenital malformation syndromes predominantly involving limbs
Q873Congenital malformation syndromes involving early overgrowth
Q8740Marfan's syndrome, unspecified
Q87410Marfan's syndrome with aortic dilation
Q87418Marfan's syndrome with other cardiovascular manifestations
Q8742Marfan's syndrome with ocular manifestations
Q8743Marfan's syndrome with skeletal manifestation
Q875Other congenital malformation syndromes with other skeletal changes
Q8781Alport syndrome
Q8782Arterial tortuosity syndrome
Q8789Other specified congenital malformation syndromes, not elsewhere classified
Q898Other specified congenital malformations
Q992Fragile X chromosome
 
PDX Collection 0541
E840Cystic fibrosis with pulmonary manifestations
E8411Meconium ileus in cystic fibrosis
E8419Cystic fibrosis with other intestinal manifestations
E848Cystic fibrosis with other manifestations
E849Cystic fibrosis, unspecified
 
PDX Collection 0542
E850Non-neuropathic heredofamilial amyloidosis
E851Neuropathic heredofamilial amyloidosis
E852Heredofamilial amyloidosis, unspecified
E853Secondary systemic amyloidosis
E854Organ-limited amyloidosis
E8581Light chain (AL) amyloidosis
E8582Wild-type transthyretin-related (ATTR) amyloidosis
E8589Other amyloidosis
E859Amyloidosis, unspecified
E8881Metabolic syndrome
 
PDX Collection 0543
E860Dehydration
E861Hypovolemia
E869Volume depletion, unspecified
E870Hyperosmolality and hypernatremia
E871Hypo-osmolality and hyponatremia
E872Acidosis
E873Alkalosis
E874Mixed disorder of acid-base balance
E875Hyperkalemia
E876Hypokalemia
E8770Fluid overload, unspecified
E8771Transfusion associated circulatory overload
E8779Other fluid overload
E878Other disorders of electrolyte and fluid balance, not elsewhere classified
 
PDX Collection 0544
E0821Diabetes mellitus due to underlying condition with diabetic nephropathy
E0822Diabetes mellitus due to underlying condition with diabetic chronic kidney disease
E0829Diabetes mellitus due to underlying condition with other diabetic kidney complication
E0921Drug or chemical induced diabetes mellitus with diabetic nephropathy
E0922Drug or chemical induced diabetes mellitus with diabetic chronic kidney disease
E0929Drug or chemical induced diabetes mellitus with other diabetic kidney complication
E883Tumor lysis syndrome
N000Acute nephritic syndrome with minor glomerular abnormality
N001Acute nephritic syndrome with focal and segmental glomerular lesions
N002Acute nephritic syndrome with diffuse membranous glomerulonephritis
N003Acute nephritic syndrome with diffuse mesangial proliferative glomerulonephritis
N004Acute nephritic syndrome with diffuse endocapillary proliferative glomerulonephritis
N005Acute nephritic syndrome with diffuse mesangiocapillary glomerulonephritis
N006Acute nephritic syndrome with dense deposit disease
N007Acute nephritic syndrome with diffuse crescentic glomerulonephritis
N008Acute nephritic syndrome with other morphologic changes
N009Acute nephritic syndrome with unspecified morphologic changes
N00AAcute nephritic syndrome with C3 glomerulonephritis
N010Rapidly progressive nephritic syndrome with minor glomerular abnormality
N011Rapidly progressive nephritic syndrome with focal and segmental glomerular lesions
N012Rapidly progressive nephritic syndrome with diffuse membranous glomerulonephritis
N013Rapidly progressive nephritic syndrome with diffuse mesangial proliferative glomerulonephritis
N014Rapidly progressive nephritic syndrome with diffuse endocapillary proliferative glomerulonephritis
N015Rapidly progressive nephritic syndrome with diffuse mesangiocapillary glomerulonephritis
N016Rapidly progressive nephritic syndrome with dense deposit disease
N017Rapidly progressive nephritic syndrome with diffuse crescentic glomerulonephritis
N018Rapidly progressive nephritic syndrome with other morphologic changes
N019Rapidly progressive nephritic syndrome with unspecified morphologic changes
N01ARapidly progressive nephritic syndrome with C3 glomerulonephritis
N028Recurrent and persistent hematuria with other morphologic changes
N029Recurrent and persistent hematuria with unspecified morphologic changes
N02ARecurrent and persistent hematuria with C3 glomerulonephritis
N047Nephrotic syndrome with diffuse crescentic glomerulonephritis
N048Nephrotic syndrome with other morphologic changes
N049Nephrotic syndrome with unspecified morphologic changes
N04ANephrotic syndrome with C3 glomerulonephritis
N050Unspecified nephritic syndrome with minor glomerular abnormality
N051Unspecified nephritic syndrome with focal and segmental glomerular lesions
N056Unspecified nephritic syndrome with dense deposit disease
N057Unspecified nephritic syndrome with diffuse crescentic glomerulonephritis
N058Unspecified nephritic syndrome with other morphologic changes
N059Unspecified nephritic syndrome with unspecified morphologic changes
N05AUnspecified nephritic syndrome with C3 glomerulonephritis
N060Isolated proteinuria with minor glomerular abnormality
N061Isolated proteinuria with focal and segmental glomerular lesions
N066Isolated proteinuria with dense deposit disease
N067Isolated proteinuria with diffuse crescentic glomerulonephritis
N068Isolated proteinuria with other morphologic lesion
N069Isolated proteinuria with unspecified morphologic lesion
N070Hereditary nephropathy, not elsewhere classified with minor glomerular abnormality
N071Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesions
N076Hereditary nephropathy, not elsewhere classified with dense deposit disease
N077Hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritis
N078Hereditary nephropathy, not elsewhere classified with other morphologic lesions
N079Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesions
N08Glomerular disorders in diseases classified elsewhere
N140Analgesic nephropathy
N141Nephropathy induced by other drugs, medicaments and biological substances
N142Nephropathy induced by unspecified drug, medicament or biological substance
N143Nephropathy induced by heavy metals
N144Toxic nephropathy, not elsewhere classified
N150Balkan nephropathy
N158Other specified renal tubulo-interstitial diseases
N159Renal tubulo-interstitial disease, unspecified
N16Renal tubulo-interstitial disorders in diseases classified elsewhere
N170Acute kidney failure with tubular necrosis
N171Acute kidney failure with acute cortical necrosis
N172Acute kidney failure with medullary necrosis
N178Other acute kidney failure
N179Acute kidney failure, unspecified
 
PDX Collection 0545
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
H49819Kearns-Sayre syndrome, unspecified eye
 
PDX Collection 0546
E368Other intraoperative complications of endocrine system
E89810Postprocedural hemorrhage of an endocrine system organ or structure following an endocrine system procedure
E89811Postprocedural hemorrhage of an endocrine system organ or structure following other procedure
E89820Postprocedural hematoma of an endocrine system organ or structure following an endocrine system procedure
E89821Postprocedural hematoma of an endocrine system organ or structure following other procedure
E89822Postprocedural seroma of an endocrine system organ or structure following an endocrine system procedure
E89823Postprocedural seroma of an endocrine system organ or structure following other procedure
E8989Other postprocedural endocrine and metabolic complications and disorders
H95811Postprocedural stenosis of right external ear canal
H95812Postprocedural stenosis of left external ear canal
H95813Postprocedural stenosis of external ear canal, bilateral
H95819Postprocedural stenosis of unspecified external ear canal
H9588Other intraoperative complications and disorders of the ear and mastoid process, not elsewhere classified
H9589Other postprocedural complications and disorders of the ear and mastoid process, not elsewhere classified
I973Postprocedural hypertension
M9689Other intraoperative and postprocedural complications and disorders of the musculoskeletal system
N981Hyperstimulation of ovaries
N982Complications of attempted introduction of fertilized ovum following in vitro fertilization
N983Complications of attempted introduction of embryo in embryo transfer
N988Other complications associated with artificial fertilization
N989Complication associated with artificial fertilization, unspecified
T8182XAEmphysema (subcutaneous) resulting from a procedure, initial encounter
T8189XAOther complications of procedures, not elsewhere classified, initial encounter
T819XXAUnspecified complication of procedure, initial encounter
 
PDX Collection 0547
F0151Vascular dementia with behavioral disturbance
 
PDX Collection 0548
F0281Dementia in other diseases classified elsewhere with behavioral disturbance
F0391Unspecified dementia with behavioral disturbance
 
PDX Collection 0549
F05Delirium due to known physiological condition
R45851Suicidal ideations
 
PDX Collection 0550
F0280Dementia in other diseases classified elsewhere without behavioral disturbance
F0281Dementia in other diseases classified elsewhere with behavioral disturbance
F04Amnestic disorder due to known physiological condition
F05Delirium due to known physiological condition
F060Psychotic disorder with hallucinations due to known physiological condition
F061Catatonic disorder due to known physiological condition
F062Psychotic disorder with delusions due to known physiological condition
F0630Mood disorder due to known physiological condition, unspecified
F0631Mood disorder due to known physiological condition with depressive features
F0632Mood disorder due to known physiological condition with major depressive-like episode
F0633Mood disorder due to known physiological condition with manic features
F0634Mood disorder due to known physiological condition with mixed features
F064Anxiety disorder due to known physiological condition
F068Other specified mental disorders due to known physiological condition
F1010Alcohol abuse, uncomplicated
F1011Alcohol abuse, in remission
F10120Alcohol abuse with intoxication, uncomplicated
F10121Alcohol abuse with intoxication delirium
F10129Alcohol abuse with intoxication, unspecified
F1014Alcohol abuse with alcohol-induced mood disorder
F10150Alcohol abuse with alcohol-induced psychotic disorder with delusions
F10151Alcohol abuse with alcohol-induced psychotic disorder with hallucinations
F10159Alcohol abuse with alcohol-induced psychotic disorder, unspecified
F10180Alcohol abuse with alcohol-induced anxiety disorder
F10181Alcohol abuse with alcohol-induced sexual dysfunction
F10182Alcohol abuse with alcohol-induced sleep disorder
F10188Alcohol abuse with other alcohol-induced disorder
F1019Alcohol abuse with unspecified alcohol-induced disorder
F1020Alcohol dependence, uncomplicated
F1021Alcohol dependence, in remission
F10220Alcohol dependence with intoxication, uncomplicated
F10221Alcohol dependence with intoxication delirium
F10229Alcohol dependence with intoxication, unspecified
F10230Alcohol dependence with withdrawal, uncomplicated
F10231Alcohol dependence with withdrawal delirium
F10232Alcohol dependence with withdrawal with perceptual disturbance
F10239Alcohol dependence with withdrawal, unspecified
F1024Alcohol dependence with alcohol-induced mood disorder
F10250Alcohol dependence with alcohol-induced psychotic disorder with delusions
F10251Alcohol dependence with alcohol-induced psychotic disorder with hallucinations
F10259Alcohol dependence with alcohol-induced psychotic disorder, unspecified
F1026Alcohol dependence with alcohol-induced persisting amnestic disorder
F1027Alcohol dependence with alcohol-induced persisting dementia
F10280Alcohol dependence with alcohol-induced anxiety disorder



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