ICD-10-CM/PCS MS-DRG v42.0 Definitions Manual

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Appendix C: Principal Diagnoses which Convert CC/MCC to non-CC
Page 304 of 430
PDX Collection 1441 (continued)
N136Pyonephrosis
N151Renal and perinephric abscess
N2882Megaloureter
N2884Pyelitis cystica
N2885Pyeloureteritis cystica
N2886Ureteritis cystica
N2889Other specified disorders of kidney and ureter
N289Disorder of kidney and ureter, unspecified
N3000Acute cystitis without hematuria
N3001Acute cystitis with hematuria
N3010Interstitial cystitis (chronic) without hematuria
N3011Interstitial cystitis (chronic) with hematuria
N3020Other chronic cystitis without hematuria
N3021Other chronic cystitis with hematuria
N3030Trigonitis without hematuria
N3031Trigonitis with hematuria
N3080Other cystitis without hematuria
N3081Other cystitis with hematuria
N3090Cystitis, unspecified without hematuria
N3091Cystitis, unspecified with hematuria
N369Urethral disorder, unspecified
N390Urinary tract infection, site not specified
N399Disorder of urinary system, 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
N99511Cystostomy infection
P392Intra-amniotic infection affecting newborn, not elsewhere classified
P393Neonatal urinary tract infection
P394Neonatal skin infection
P398Other specified infections specific to the perinatal period
P399Infection specific to the perinatal period, unspecified
R300Dysuria
R309Painful micturition, unspecified
R8271Bacteriuria
T83511AInfection and inflammatory reaction due to indwelling urethral catheter, initial encounter
 
PDX Collection 1442
P290Neonatal cardiac failure
P2911Neonatal tachycardia
P2912Neonatal bradycardia
P292Neonatal hypertension
P294Transient myocardial ischemia in newborn
P2989Other cardiovascular disorders originating in the perinatal period
P299Cardiovascular disorder originating in the perinatal period, unspecified
P53Hemorrhagic disease of newborn
P60Disseminated intravascular coagulation of newborn
P610Transient neonatal thrombocytopenia
P611Polycythemia neonatorum
P612Anemia of prematurity
P613Congenital anemia from fetal blood loss
P614Other congenital anemias, not elsewhere classified
P615Transient neonatal neutropenia
P616Other transient neonatal disorders of coagulation
P618Other specified perinatal hematological disorders
P619Perinatal hematological disorder, unspecified
P941Congenital hypertonia
P942Congenital hypotonia
P948Other disorders of muscle tone of newborn
P949Disorder of muscle tone of newborn, unspecified
P960Congenital renal failure
P963Wide cranial sutures of newborn
P965Complication to newborn due to (fetal) intrauterine procedure
P9682Delayed separation of umbilical cord
P9683Meconium staining
P9689Other specified conditions originating in the perinatal period
 
PDX Collection 1443
P290Neonatal cardiac failure
P2911Neonatal tachycardia
P2912Neonatal bradycardia
P292Neonatal hypertension
P294Transient myocardial ischemia in newborn
P2989Other cardiovascular disorders originating in the perinatal period
P299Cardiovascular disorder originating in the perinatal period, unspecified
P500Newborn affected by intrauterine (fetal) blood loss from vasa previa
P501Newborn affected by intrauterine (fetal) blood loss from ruptured cord
P502Newborn affected by intrauterine (fetal) blood loss from placenta
P503Newborn affected by hemorrhage into co-twin
P504Newborn affected by hemorrhage into maternal circulation
P505Newborn affected by intrauterine (fetal) blood loss from cut end of co-twin's cord
P508Newborn affected by other intrauterine (fetal) blood loss
P509Newborn affected by intrauterine (fetal) blood loss, unspecified
P53Hemorrhagic disease of newborn
P540Neonatal hematemesis
P541Neonatal melena
P542Neonatal rectal hemorrhage
P543Other neonatal gastrointestinal hemorrhage
P544Neonatal adrenal hemorrhage
P546Neonatal vaginal hemorrhage
P548Other specified neonatal hemorrhages
P549Neonatal hemorrhage, unspecified
P60Disseminated intravascular coagulation of newborn
P610Transient neonatal thrombocytopenia
P611Polycythemia neonatorum
P612Anemia of prematurity
P613Congenital anemia from fetal blood loss
P614Other congenital anemias, not elsewhere classified
P615Transient neonatal neutropenia
P616Other transient neonatal disorders of coagulation
P618Other specified perinatal hematological disorders
P619Perinatal hematological disorder, unspecified
P941Congenital hypertonia
P942Congenital hypotonia
P948Other disorders of muscle tone of newborn
P949Disorder of muscle tone of newborn, unspecified
P960Congenital renal failure
P963Wide cranial sutures of newborn
P965Complication to newborn due to (fetal) intrauterine procedure
P9682Delayed separation of umbilical cord
P9683Meconium staining
P9689Other specified conditions originating in the perinatal period
 
PDX Collection 1444
P290Neonatal cardiac failure
P2911Neonatal tachycardia
P2912Neonatal bradycardia
P292Neonatal hypertension
P294Transient myocardial ischemia in newborn
P2989Other cardiovascular disorders originating in the perinatal period
P299Cardiovascular disorder originating in the perinatal period, unspecified
P550Rh isoimmunization of newborn
P551ABO isoimmunization of newborn
P558Other hemolytic diseases of newborn
P559Hemolytic disease of newborn, unspecified
P560Hydrops fetalis due to isoimmunization
P5690Hydrops fetalis due to unspecified hemolytic disease
P5699Hydrops fetalis due to other hemolytic disease
P570Kernicterus due to isoimmunization
P941Congenital hypertonia
P942Congenital hypotonia
P948Other disorders of muscle tone of newborn
P949Disorder of muscle tone of newborn, unspecified
P960Congenital renal failure
P963Wide cranial sutures of newborn
P965Complication to newborn due to (fetal) intrauterine procedure
P9682Delayed separation of umbilical cord
P9683Meconium staining
P9689Other specified conditions originating in the perinatal period
 
PDX Collection 1445
P290Neonatal cardiac failure
P2911Neonatal tachycardia
P2912Neonatal bradycardia
P292Neonatal hypertension
P294Transient myocardial ischemia in newborn
P2989Other cardiovascular disorders originating in the perinatal period
P299Cardiovascular disorder originating in the perinatal period, unspecified
P578Other specified kernicterus
P579Kernicterus, unspecified
P580Neonatal jaundice due to bruising
P581Neonatal jaundice due to bleeding
P582Neonatal jaundice due to infection
P583Neonatal jaundice due to polycythemia
P5841Neonatal jaundice due to drugs or toxins transmitted from mother
P5842Neonatal jaundice due to drugs or toxins given to newborn
P585Neonatal jaundice due to swallowed maternal blood
P588Neonatal jaundice due to other specified excessive hemolysis
P589Neonatal jaundice due to excessive hemolysis, unspecified
P590Neonatal jaundice associated with preterm delivery
P591Inspissated bile syndrome
P5920Neonatal jaundice from unspecified hepatocellular damage
P5929Neonatal jaundice from other hepatocellular damage
P593Neonatal jaundice from breast milk inhibitor
P598Neonatal jaundice from other specified causes
P599Neonatal jaundice, unspecified
P941Congenital hypertonia
P942Congenital hypotonia
P948Other disorders of muscle tone of newborn
P949Disorder of muscle tone of newborn, unspecified
P960Congenital renal failure
P963Wide cranial sutures of newborn
P965Complication to newborn due to (fetal) intrauterine procedure
P9682Delayed separation of umbilical cord
P9683Meconium staining
P9689Other specified conditions originating in the perinatal period
 
PDX Collection 1446
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
D553Anemia due to disorders of nucleotide metabolism
D558Other anemias due to enzyme disorders
D559Anemia due to enzyme disorder, unspecified
D564Hereditary persistence of fetal hemoglobin [HPFH]
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
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
D6103Fanconi anemia
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
D759Disease of blood and blood-forming organs, unspecified
P612Anemia of prematurity
P613Congenital anemia from fetal blood loss
P614Other congenital anemias, not elsewhere classified
 
PDX Collection 1447
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
D564Hereditary persistence of fetal hemoglobin [HPFH]
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
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
D6103Fanconi anemia
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
D759Disease of blood and blood-forming organs, unspecified
P612Anemia of prematurity
P613Congenital anemia from fetal blood loss
P614Other congenital anemias, not elsewhere classified
 
PDX Collection 1448
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
D564Hereditary persistence of fetal hemoglobin [HPFH]
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
D573Sickle-cell trait
D57811Other sickle-cell disorders with acute chest syndrome
D57812Other sickle-cell disorders with splenic sequestration
D57819Other sickle-cell disorders with crisis, unspecified
D582Other hemoglobinopathies
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
D5930Hemolytic-uremic syndrome, unspecified
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