ICD-10-CM/PCS MS-DRG v41.0 Definitions Manual

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Appendix C: Principal diagnoses which convert CC/MCC to non-CC
Page 1283 of 1324
PDX Collection 6917 (continued)
N044Nephrotic syndrome with diffuse endocapillary proliferative glomerulonephritis
N045Nephrotic syndrome with diffuse mesangiocapillary glomerulonephritis
N046Nephrotic syndrome with dense deposit disease
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
N052Unspecified nephritic syndrome with diffuse membranous glomerulonephritis
N053Unspecified nephritic syndrome with diffuse mesangial proliferative glomerulonephritis
N054Unspecified nephritic syndrome with diffuse endocapillary proliferative glomerulonephritis
N055Unspecified nephritic syndrome with diffuse mesangiocapillary glomerulonephritis
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
N0620Isolated proteinuria with diffuse membranous glomerulonephritis, unspecified
N0621Primary membranous nephropathy with isolated proteinuria
N0622Secondary membranous nephropathy with isolated proteinuria
N0629Other isolated proteinuria with diffuse membranous glomerulonephritis
N063Isolated proteinuria with diffuse mesangial proliferative glomerulonephritis
N064Isolated proteinuria with diffuse endocapillary proliferative glomerulonephritis
N065Isolated proteinuria with diffuse mesangiocapillary glomerulonephritis
N066Isolated proteinuria with dense deposit disease
N067Isolated proteinuria with diffuse crescentic glomerulonephritis
N068Isolated proteinuria with other morphologic lesion
N069Isolated proteinuria with unspecified morphologic lesion
N06AIsolated proteinuria with C3 glomerulonephritis
N070Hereditary nephropathy, not elsewhere classified with minor glomerular abnormality
N071Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesions
N072Hereditary nephropathy, not elsewhere classified with diffuse membranous glomerulonephritis
N073Hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritis
N074Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritis
N075Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis
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
N07AHereditary nephropathy, not elsewhere classified with C3 glomerulonephritis
N118Other chronic tubulo-interstitial nephritis
N119Chronic tubulo-interstitial nephritis, unspecified
N12Tubulo-interstitial nephritis, not specified as acute or chronic
N1411Contrast-induced nephropathy
N1419Nephropathy induced by other drugs, medicaments and biological substances
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
N80A0Endometriosis of bladder, unspecified depth
N80A1Superficial endometriosis of bladder
N80A2Deep endometriosis of bladder
N80A41Superficial endometriosis of right ureter
N80A42Superficial endometriosis of left ureter
N80A43Superficial endometriosis of bilateral ureters
N80A49Superficial endometriosis of unspecified ureter
N80A51Deep endometriosis of right ureter
N80A52Deep endometriosis of left ureter
N80A53Deep endometriosis of bilateral ureters
N80A59Deep endometriosis of unspecified ureter
N80A61Endometriosis of right ureter, unspecified depth
N80A62Endometriosis of left ureter, unspecified depth
N80A63Endometriosis of bilateral ureters, unspecified depth
N80A69Endometriosis of unspecified ureter, unspecified depth
 
PDX Collection 6918
D474Osteomyelofibrosis
D500Iron deficiency anemia secondary to blood loss (chronic)
D501Sideropenic dysphagia
D508Other iron deficiency anemias
D509Iron deficiency anemia, unspecified
D510Vitamin B12 deficiency anemia due to intrinsic factor deficiency
D511Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria
D512Transcobalamin II deficiency
D513Other dietary vitamin B12 deficiency anemia
D518Other vitamin B12 deficiency anemias
D519Vitamin B12 deficiency anemia, unspecified
D520Dietary folate deficiency anemia
D521Drug-induced folate deficiency anemia
D528Other folate deficiency anemias
D529Folate deficiency anemia, unspecified
D530Protein deficiency anemia
D531Other megaloblastic anemias, not elsewhere classified
D532Scorbutic anemia
D538Other specified nutritional anemias
D539Nutritional anemia, unspecified
D550Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
D551Anemia due to other disorders of glutathione metabolism
D5521Anemia due to pyruvate kinase deficiency
D5529Anemia due to other disorders of glycolytic enzymes
D553Anemia due to disorders of nucleotide metabolism
D558Other anemias due to enzyme disorders
D559Anemia due to enzyme disorder, unspecified
D560Alpha thalassemia
D561Beta thalassemia
D562Delta-beta thalassemia
D563Thalassemia minor
D564Hereditary persistence of fetal hemoglobin [HPFH]
D565Hemoglobin E-beta thalassemia
D568Other thalassemias
D569Thalassemia, unspecified
D5700Hb-SS disease with crisis, unspecified
D5701Hb-SS disease with acute chest syndrome
D5702Hb-SS disease with splenic sequestration
D571Sickle-cell disease without crisis
D5720Sickle-cell/Hb-C disease without crisis
D57211Sickle-cell/Hb-C disease with acute chest syndrome
D57212Sickle-cell/Hb-C disease with splenic sequestration
D57213Sickle-cell/Hb-C disease with cerebral vascular involvement
D57214Sickle-cell/Hb-C disease with dactylitis
D57218Sickle-cell/Hb-C disease with crisis with other specified complication
D57219Sickle-cell/Hb-C disease with crisis, unspecified
D573Sickle-cell trait
D5740Sickle-cell thalassemia without crisis
D57411Sickle-cell thalassemia, unspecified, with acute chest syndrome
D57412Sickle-cell thalassemia, unspecified, with splenic sequestration
D57419Sickle-cell thalassemia, unspecified, with crisis
D5780Other sickle-cell disorders without crisis
D57811Other sickle-cell disorders with acute chest syndrome
D57812Other sickle-cell disorders with splenic sequestration
D57819Other sickle-cell disorders with crisis, unspecified
D580Hereditary spherocytosis
D581Hereditary elliptocytosis
D582Other hemoglobinopathies
D588Other specified hereditary hemolytic anemias
D589Hereditary hemolytic anemia, unspecified
D590Drug-induced autoimmune hemolytic anemia
D5910Autoimmune hemolytic anemia, unspecified
D5911Warm autoimmune hemolytic anemia
D5912Cold autoimmune hemolytic anemia
D5913Mixed type autoimmune hemolytic anemia
D5919Other autoimmune hemolytic anemia
D592Drug-induced nonautoimmune hemolytic anemia
D5930Hemolytic-uremic syndrome, unspecified
D5931Infection-associated hemolytic-uremic syndrome
D5932Hereditary hemolytic-uremic syndrome
D5939Other hemolytic-uremic syndrome
D594Other nonautoimmune hemolytic anemias
D595Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]
D596Hemoglobinuria due to hemolysis from other external causes
D598Other acquired hemolytic anemias
D599Acquired hemolytic anemia, unspecified
D600Chronic acquired pure red cell aplasia
D601Transient acquired pure red cell aplasia
D608Other acquired pure red cell aplasias
D609Acquired pure red cell aplasia, unspecified
D6101Constitutional (pure) red blood cell aplasia
D6102Shwachman-Diamond syndrome
D6109Other constitutional aplastic anemia
D611Drug-induced aplastic anemia
D612Aplastic anemia due to other external agents
D613Idiopathic aplastic anemia
D61810Antineoplastic chemotherapy induced pancytopenia
D61811Other drug-induced pancytopenia
D61818Other pancytopenia
D6182Myelophthisis
D6189Other specified aplastic anemias and other bone marrow failure syndromes
D619Aplastic anemia, unspecified
D62Acute posthemorrhagic anemia
D640Hereditary sideroblastic anemia
D642Secondary sideroblastic anemia due to drugs and toxins
D643Other sideroblastic anemias
D644Congenital dyserythropoietic anemia
D6481Anemia due to antineoplastic chemotherapy
D6489Other specified anemias
D649Anemia, unspecified
D68312Antiphospholipid antibody with hemorrhagic disorder
D6851Activated protein C resistance
D6852Prothrombin gene mutation
D6859Other primary thrombophilia
D6861Antiphospholipid syndrome
D6862Lupus anticoagulant syndrome
D6869Other thrombophilia
D7589Other specified diseases of blood and blood-forming organs
D759Disease of blood and blood-forming organs, unspecified
D75AGlucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia
D892Hypergammaglobulinemia, unspecified
 
PDX Collection 6919
A020Salmonella enteritis
A039Shigellosis, unspecified
A040Enteropathogenic Escherichia coli infection
A041Enterotoxigenic Escherichia coli infection
A042Enteroinvasive Escherichia coli infection
A043Enterohemorrhagic Escherichia coli infection
A044Other intestinal Escherichia coli infections
A045Campylobacter enteritis
A046Enteritis due to Yersinia enterocolitica
A0471Enterocolitis due to Clostridium difficile, recurrent
A0472Enterocolitis due to Clostridium difficile, not specified as recurrent
A048Other specified bacterial intestinal infections
A049Bacterial intestinal infection, unspecified
A050Foodborne staphylococcal intoxication
A052Foodborne Clostridium perfringens [Clostridium welchii] intoxication
A060Acute amebic dysentery
A061Chronic intestinal amebiasis
A062Amebic nondysenteric colitis
A069Amebiasis, unspecified
A071Giardiasis [lambliasis]
A072Cryptosporidiosis
A073Isosporiasis
A074Cyclosporiasis
A078Other specified protozoal intestinal diseases
A079Protozoal intestinal disease, unspecified
A080Rotaviral enteritis
A0811Acute gastroenteropathy due to Norwalk agent
A0819Acute gastroenteropathy due to other small round viruses
A082Adenoviral enteritis
A0831Calicivirus enteritis
A0832Astrovirus enteritis
A0839Other viral enteritis
A084Viral intestinal infection, unspecified
A088Other specified intestinal infections
A09Infectious gastroenteritis and colitis, unspecified
A1832Tuberculous enteritis
A1839Retroperitoneal tuberculosis
A1883Tuberculosis of digestive tract organs, not elsewhere classified
B3782Candidal enteritis
B829Intestinal parasitism, unspecified
J09X3Influenza due to identified novel influenza A virus with gastrointestinal manifestations
J09X9Influenza due to identified novel influenza A virus with other manifestations
J102Influenza due to other identified influenza virus with gastrointestinal manifestations
J1081Influenza due to other identified influenza virus with encephalopathy
J1082Influenza due to other identified influenza virus with myocarditis
J1083Influenza due to other identified influenza virus with otitis media
J1089Influenza due to other identified influenza virus with other manifestations
J112Influenza due to unidentified influenza virus with gastrointestinal manifestations
J1181Influenza due to unidentified influenza virus with encephalopathy
J1182Influenza due to unidentified influenza virus with myocarditis
J1183Influenza due to unidentified influenza virus with otitis media
J1189Influenza due to unidentified influenza virus with other manifestations
K30Functional dyspepsia
K3184Gastroparesis
K521Toxic gastroenteritis and colitis
K5221Food protein-induced enterocolitis syndrome
K5222Food protein-induced enteropathy
K5229Other allergic and dietetic gastroenteritis and colitis
K523Indeterminate colitis
K5282Eosinophilic colitis
K52831Collagenous colitis
K52832Lymphocytic colitis
K52838Other microscopic colitis
K52839Microscopic colitis, unspecified
K5289Other specified noninfective gastroenteritis and colitis
K529Noninfective gastroenteritis and colitis, unspecified
K580Irritable bowel syndrome with diarrhea
K581Irritable bowel syndrome with constipation
K582Mixed irritable bowel syndrome
K588Other irritable bowel syndrome
K589Irritable bowel syndrome without diarrhea
K650Generalized (acute) peritonitis
K652Spontaneous bacterial peritonitis
K658Other peritonitis
K6812Psoas muscle abscess
K6819Other retroperitoneal abscess
K682Retroperitoneal fibrosis
K683Retroperitoneal hematoma
K689Other disorders of retroperitoneum
P768Other specified intestinal obstruction of newborn
P769Intestinal obstruction of newborn, unspecified
P771Stage 1 necrotizing enterocolitis in newborn
P772Stage 2 necrotizing enterocolitis in newborn
P773Stage 3 necrotizing enterocolitis in newborn
P779Necrotizing enterocolitis in newborn, unspecified
P781Other neonatal peritonitis
P783Noninfective neonatal diarrhea
P7881Congenital cirrhosis (of liver)
P7882Peptic ulcer of newborn
P7883Newborn esophageal reflux
P7884Gestational alloimmune liver disease
P7889Other specified perinatal digestive system disorders
 
PDX Collection 6920
A020Salmonella enteritis
A039Shigellosis, unspecified
A040Enteropathogenic Escherichia coli infection
A041Enterotoxigenic Escherichia coli infection
A042Enteroinvasive Escherichia coli infection
A043Enterohemorrhagic Escherichia coli infection
A044Other intestinal Escherichia coli infections
A045Campylobacter enteritis
A046Enteritis due to Yersinia enterocolitica
A0471Enterocolitis due to Clostridium difficile, recurrent
A0472Enterocolitis due to Clostridium difficile, not specified as recurrent
A048Other specified bacterial intestinal infections
A049Bacterial intestinal infection, unspecified
A050Foodborne staphylococcal intoxication
A052Foodborne Clostridium perfringens [Clostridium welchii] intoxication
A060Acute amebic dysentery
A061Chronic intestinal amebiasis
A062Amebic nondysenteric colitis
A069Amebiasis, unspecified
A071Giardiasis [lambliasis]
A072Cryptosporidiosis
A073Isosporiasis
A074Cyclosporiasis
A078Other specified protozoal intestinal diseases
A079Protozoal intestinal disease, unspecified
A080Rotaviral enteritis
A0811Acute gastroenteropathy due to Norwalk agent
A0819Acute gastroenteropathy due to other small round viruses
A082Adenoviral enteritis
A0831Calicivirus enteritis
A0832Astrovirus enteritis
A0839Other viral enteritis
A084Viral intestinal infection, unspecified
A088Other specified intestinal infections
A09Infectious gastroenteritis and colitis, unspecified
A1832Tuberculous enteritis
A1839Retroperitoneal tuberculosis
A1883Tuberculosis of digestive tract organs, not elsewhere classified
B3782Candidal enteritis
B829Intestinal parasitism, unspecified
J09X3Influenza due to identified novel influenza A virus with gastrointestinal manifestations
J09X9Influenza due to identified novel influenza A virus with other manifestations
J102Influenza due to other identified influenza virus with gastrointestinal manifestations
J1081Influenza due to other identified influenza virus with encephalopathy
J1082Influenza due to other identified influenza virus with myocarditis
J1083Influenza due to other identified influenza virus with otitis media
J1089Influenza due to other identified influenza virus with other manifestations
J112Influenza due to unidentified influenza virus with gastrointestinal manifestations
J1181Influenza due to unidentified influenza virus with encephalopathy
J1182Influenza due to unidentified influenza virus with myocarditis
J1183Influenza due to unidentified influenza virus with otitis media
J1189Influenza due to unidentified influenza virus with other manifestations
K30Functional dyspepsia
K3184Gastroparesis
K521Toxic gastroenteritis and colitis
K5221Food protein-induced enterocolitis syndrome
K5222Food protein-induced enteropathy
K5229Other allergic and dietetic gastroenteritis and colitis
K523Indeterminate colitis
K5282Eosinophilic colitis
K52831Collagenous colitis
K52832Lymphocytic colitis
K52838Other microscopic colitis
K52839Microscopic colitis, unspecified
K5289Other specified noninfective gastroenteritis and colitis
K529Noninfective gastroenteritis and colitis, unspecified
K580Irritable bowel syndrome with diarrhea
K581Irritable bowel syndrome with constipation
K582Mixed irritable bowel syndrome
K588Other irritable bowel syndrome
K589Irritable bowel syndrome without diarrhea
K650Generalized (acute) peritonitis
K652Spontaneous bacterial peritonitis
K658Other peritonitis
K6812Psoas muscle abscess
K6819Other retroperitoneal abscess
K682Retroperitoneal fibrosis
K683Retroperitoneal hematoma
K689Other disorders of retroperitoneum
P768Other specified intestinal obstruction of newborn
P769Intestinal obstruction of newborn, unspecified
P771Stage 1 necrotizing enterocolitis in newborn
P772Stage 2 necrotizing enterocolitis in newborn
P773Stage 3 necrotizing enterocolitis in newborn
P779Necrotizing enterocolitis in newborn, unspecified
P781Other neonatal peritonitis
P783Noninfective neonatal diarrhea
P7881Congenital cirrhosis (of liver)
P7882Peptic ulcer of newborn
P7883Newborn esophageal reflux
P7884Gestational alloimmune liver disease
P7889Other specified perinatal digestive system disorders
 
PDX Collection 6921
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
E7153Other group 2 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
E8843Disorders of mitochondrial tRNA synthetases
E8849Other mitochondrial metabolism disorders
E88811Insulin resistance syndrome, Type A
E88818Other insulin resistance
E88819Insulin resistance, unspecified
E8889Other specified metabolic disorders
H49811Kearns-Sayre syndrome, right eye
H49812Kearns-Sayre syndrome, left eye
H49813Kearns-Sayre syndrome, bilateral
H49819Kearns-Sayre syndrome, unspecified eye



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