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 1130 of 1324
PDX Collection 6250 (continued)
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 6251
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
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 6252
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
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 6253
K634Enteroptosis
K6389Other specified diseases of intestine
K639Disease of intestine, unspecified
K650Generalized (acute) peritonitis
K651Peritoneal abscess
K652Spontaneous bacterial peritonitis
K653Choleperitonitis
K654Sclerosing mesenteritis
K658Other peritonitis
K659Peritonitis, unspecified
K6819Other retroperitoneal abscess
K683Retroperitoneal hematoma
K689Other disorders of retroperitoneum
K9289Other specified diseases of the digestive system
K929Disease of digestive system, unspecified
R1113Vomiting of fecal matter
 
PDX Collection 6254
Q440Agenesis, aplasia and hypoplasia of gallbladder
Q441Other congenital malformations of gallbladder
Q442Atresia of bile ducts
Q443Congenital stenosis and stricture of bile ducts
Q444Choledochal cyst
Q445Other congenital malformations of bile ducts
Q446Cystic disease of liver
Q4470Other congenital malformation of liver, unspecified
Q4471Alagille syndrome
Q4479Other congenital malformations of liver
 
PDX Collection 6255
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
E88811Insulin resistance syndrome, Type A
E88818Other insulin resistance
E88819Insulin resistance, unspecified
E8889Other specified metabolic disorders
H49819Kearns-Sayre syndrome, unspecified eye
 
PDX Collection 6256
K634Enteroptosis
K6389Other specified diseases of intestine
K639Disease of intestine, unspecified
K650Generalized (acute) peritonitis
K651Peritoneal abscess
K652Spontaneous bacterial peritonitis
K653Choleperitonitis
K654Sclerosing mesenteritis
K658Other peritonitis
K659Peritonitis, unspecified
K6819Other retroperitoneal abscess
K682Retroperitoneal fibrosis
K689Other disorders of retroperitoneum
K9289Other specified diseases of the digestive system
K929Disease of digestive system, unspecified
R1113Vomiting of fecal matter
 
PDX Collection 6257
Q440Agenesis, aplasia and hypoplasia of gallbladder
Q441Other congenital malformations of gallbladder
Q442Atresia of bile ducts
Q443Congenital stenosis and stricture of bile ducts
Q444Choledochal cyst
Q445Other congenital malformations of bile ducts
Q446Cystic disease of liver
Q4470Other congenital malformation of liver, unspecified
Q4471Alagille syndrome
Q4479Other congenital malformations of liver
 
PDX Collection 6258
D800Hereditary hypogammaglobulinemia
D803Selective deficiency of immunoglobulin G [IgG] subclasses
D804Selective deficiency of immunoglobulin M [IgM]
D805Immunodeficiency with increased immunoglobulin M [IgM]
D806Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
D807Transient hypogammaglobulinemia of infancy
D808Other immunodeficiencies with predominantly antibody defects
D809Immunodeficiency with predominantly antibody defects, unspecified
D810Severe combined immunodeficiency [SCID] with reticular dysgenesis
D811Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
D812Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
D814Nezelof's syndrome
D816Major histocompatibility complex class I deficiency
D817Major histocompatibility complex class II deficiency
D8182Activated Phosphoinositide 3-kinase Delta Syndrome [APDS]
D8189Other combined immunodeficiencies
D819Combined immunodeficiency, unspecified
D820Wiskott-Aldrich syndrome
D821Di George's syndrome
D822Immunodeficiency with short-limbed stature
D823Immunodeficiency following hereditary defective response to Epstein-Barr virus
D824Hyperimmunoglobulin E [IgE] syndrome
D828Immunodeficiency associated with other specified major defects
D829Immunodeficiency associated with major defect, unspecified
D830Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
D831Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
D832Common variable immunodeficiency with autoantibodies to B- or T-cells
D838Other common variable immunodeficiencies
D839Common variable immunodeficiency, unspecified
D840Lymphocyte function antigen-1 [LFA-1] defect
D84821Immunodeficiency due to drugs
D84822Immunodeficiency due to external causes
D8489Other immunodeficiencies
D849Immunodeficiency, unspecified
D893Immune reconstitution syndrome
D8940Mast cell activation, unspecified
D8941Monoclonal mast cell activation syndrome
D8942Idiopathic mast cell activation syndrome
D8943Secondary mast cell activation
D8949Other mast cell activation disorder
D8982Autoimmune lymphoproliferative syndrome [ALPS]
D8984IgG4-related disease
D8989Other specified disorders involving the immune mechanism, not elsewhere classified
D899Disorder involving the immune mechanism, unspecified
 
PDX Collection 6259
D800Hereditary hypogammaglobulinemia
D803Selective deficiency of immunoglobulin G [IgG] subclasses
D804Selective deficiency of immunoglobulin M [IgM]
D805Immunodeficiency with increased immunoglobulin M [IgM]
D806Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
D807Transient hypogammaglobulinemia of infancy
D808Other immunodeficiencies with predominantly antibody defects
D809Immunodeficiency with predominantly antibody defects, unspecified
D810Severe combined immunodeficiency [SCID] with reticular dysgenesis
D811Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
D812Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
D814Nezelof's syndrome
D816Major histocompatibility complex class I deficiency
D817Major histocompatibility complex class II deficiency
D8182Activated Phosphoinositide 3-kinase Delta Syndrome [APDS]



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13 Oct 2023 12:52:35
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