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 1312 of 1324
PDX Collection 6984 (continued)
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
D5703Hb-SS disease with cerebral vascular involvement
D5704Hb-SS disease with dactylitis
D5709Hb-SS disease with crisis with other specified complication
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
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
D57413Sickle-cell thalassemia, unspecified, with cerebral vascular involvement
D57414Sickle-cell thalassemia, unspecified, with dactylitis
D57418Sickle-cell thalassemia, unspecified, with crisis with other specified complication
D57419Sickle-cell thalassemia, unspecified, with crisis
D5742Sickle-cell thalassemia beta zero without crisis
D57431Sickle-cell thalassemia beta zero with acute chest syndrome
D57432Sickle-cell thalassemia beta zero with splenic sequestration
D57433Sickle-cell thalassemia beta zero with cerebral vascular involvement
D57434Sickle-cell thalassemia beta zero with dactylitis
D57438Sickle-cell thalassemia beta zero with crisis with other specified complication
D57439Sickle-cell thalassemia beta zero with crisis, unspecified
D5744Sickle-cell thalassemia beta plus without crisis
D57451Sickle-cell thalassemia beta plus with acute chest syndrome
D57452Sickle-cell thalassemia beta plus with splenic sequestration
D57453Sickle-cell thalassemia beta plus with cerebral vascular involvement
D57454Sickle-cell thalassemia beta plus with dactylitis
D57458Sickle-cell thalassemia beta plus with crisis with other specified complication
D57459Sickle-cell thalassemia beta plus with crisis, unspecified
D5780Other sickle-cell disorders without crisis
D57811Other sickle-cell disorders with acute chest syndrome
D57812Other sickle-cell disorders with splenic sequestration
D57813Other sickle-cell disorders with cerebral vascular involvement
D57814Other sickle-cell disorders with dactylitis
D57818Other sickle-cell disorders with crisis with other specified complication
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
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 6985
C880Waldenstrom macroglobulinemia
D472Monoclonal gammopathy
D890Polyclonal hypergammaglobulinemia
D891Cryoglobulinemia
E700Classical phenylketonuria
E701Other hyperphenylalaninemias
E7020Disorder of tyrosine metabolism, unspecified
E7021Tyrosinemia
E7029Other disorders of tyrosine metabolism
E7030Albinism, unspecified
E70310X-linked ocular albinism
E70311Autosomal recessive ocular albinism
E70318Other ocular albinism
E70319Ocular albinism, unspecified
E70320Tyrosinase negative oculocutaneous albinism
E70321Tyrosinase positive oculocutaneous albinism
E70328Other oculocutaneous albinism
E70329Oculocutaneous albinism, unspecified
E70330Chediak-Higashi syndrome
E70331Hermansky-Pudlak syndrome
E70338Other albinism with hematologic abnormality
E70339Albinism with hematologic abnormality, unspecified
E7039Other specified albinism
E7040Disorders of histidine metabolism, unspecified
E7041Histidinemia
E7049Other disorders of histidine metabolism
E705Disorders of tryptophan metabolism
E7081Aromatic L-amino acid decarboxylase deficiency
E7089Other disorders of aromatic amino-acid metabolism
E709Disorder of aromatic amino-acid metabolism, unspecified
E710Maple-syrup-urine disease
E71110Isovaleric acidemia
E711113-methylglutaconic aciduria
E71118Other branched-chain organic acidurias
E71120Methylmalonic acidemia
E71121Propionic acidemia
E71128Other disorders of propionate metabolism
E7119Other disorders of branched-chain amino-acid metabolism
E712Disorder of branched-chain amino-acid metabolism, unspecified
E7130Disorder of fatty-acid metabolism, unspecified
E7200Disorders of amino-acid transport, unspecified
E7201Cystinuria
E7202Hartnup's disease
E7204Cystinosis
E7209Other disorders of amino-acid transport
E7210Disorders of sulfur-bearing amino-acid metabolism, unspecified
E7211Homocystinuria
E7212Methylenetetrahydrofolate reductase deficiency
E7219Other disorders of sulfur-bearing amino-acid metabolism
E7220Disorder of urea cycle metabolism, unspecified
E7221Argininemia
E7222Arginosuccinic aciduria
E7223Citrullinemia
E7229Other disorders of urea cycle metabolism
E723Disorders of lysine and hydroxylysine metabolism
E724Disorders of ornithine metabolism
E7250Disorder of glycine metabolism, unspecified
E7251Non-ketotic hyperglycinemia
E7252Trimethylaminuria
E7253Primary hyperoxaluria
E7259Other disorders of glycine metabolism
E7281Disorders of gamma aminobutyric acid metabolism
E7289Other specified disorders of amino-acid metabolism
E729Disorder of amino-acid metabolism, unspecified
E730Congenital lactase deficiency
E731Secondary lactase deficiency
E738Other lactose intolerance
E739Lactose intolerance, unspecified
E7400Glycogen storage disease, unspecified
E7401von Gierke disease
E7402Pompe disease
E7403Cori disease
E7404McArdle disease
E7405Lysosome-associated membrane protein 2 [LAMP2] deficiency
E7409Other glycogen storage disease
E7410Disorder of fructose metabolism, unspecified
E7411Essential fructosuria
E7412Hereditary fructose intolerance
E7419Other disorders of fructose metabolism
E7420Disorders of galactose metabolism, unspecified
E7421Galactosemia
E7429Other disorders of galactose metabolism
E7431Sucrase-isomaltase deficiency
E7439Other disorders of intestinal carbohydrate absorption
E744Disorders of pyruvate metabolism and gluconeogenesis
E74810Glucose transporter protein type 1 deficiency
E74818Other disorders of glucose transport
E74819Disorders of glucose transport, unspecified
E7489Other specified disorders of carbohydrate metabolism
E749Disorder of carbohydrate metabolism, unspecified
E7521Fabry (-Anderson) disease
E7522Gaucher disease
E75240Niemann-Pick disease type A
E75241Niemann-Pick disease type B
E75242Niemann-Pick disease type C
E75243Niemann-Pick disease type D
E75248Other Niemann-Pick disease
E75249Niemann-Pick disease, unspecified
E753Sphingolipidosis, unspecified
E755Other lipid storage disorders
E756Lipid storage disorder, unspecified
E770Defects in post-translational modification of lysosomal enzymes
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
E88811Insulin resistance syndrome, Type A
E88818Other insulin resistance
E88819Insulin resistance, unspecified
E8889Other specified metabolic disorders
 
PDX Collection 6986
I0981Rheumatic heart failure
I110Hypertensive heart disease with heart failure
I130Hypertensive heart and chronic kidney disease with heart failure and stage 1 through stage 4 chronic kidney disease, or unspecified chronic kidney disease
I132Hypertensive heart and chronic kidney disease with heart failure and with stage 5 chronic kidney disease, or end stage renal disease
I200Unstable angina
I201Angina pectoris with documented spasm
I202Refractory angina pectoris
I2081Angina pectoris with coronary microvascular dysfunction
I2089Other forms of angina pectoris
I209Angina pectoris, unspecified
I2101ST elevation (STEMI) myocardial infarction involving left main coronary artery
I2102ST elevation (STEMI) myocardial infarction involving left anterior descending coronary artery
I2109ST elevation (STEMI) myocardial infarction involving other coronary artery of anterior wall
I2111ST elevation (STEMI) myocardial infarction involving right coronary artery
I2119ST elevation (STEMI) myocardial infarction involving other coronary artery of inferior wall
I2121ST elevation (STEMI) myocardial infarction involving left circumflex coronary artery
I2129ST elevation (STEMI) myocardial infarction involving other sites
I213ST elevation (STEMI) myocardial infarction of unspecified site
I214Non-ST elevation (NSTEMI) myocardial infarction
I219Acute myocardial infarction, unspecified
I21A1Myocardial infarction type 2
I21A9Other myocardial infarction type
I21BMyocardial infarction with coronary microvascular dysfunction
I220Subsequent ST elevation (STEMI) myocardial infarction of anterior wall
I221Subsequent ST elevation (STEMI) myocardial infarction of inferior wall
I222Subsequent non-ST elevation (NSTEMI) myocardial infarction
I228Subsequent ST elevation (STEMI) myocardial infarction of other sites
I229Subsequent ST elevation (STEMI) myocardial infarction of unspecified site
I240Acute coronary thrombosis not resulting in myocardial infarction
I2481Acute coronary microvascular dysfunction
I2489Other forms of acute ischemic heart disease
I249Acute ischemic heart disease, unspecified
I255Ischemic cardiomyopathy
I256Silent myocardial ischemia
I25700Atherosclerosis of coronary artery bypass graft(s), unspecified, with unstable angina pectoris
I25702Atherosclerosis of coronary artery bypass graft(s), unspecified, with refractory angina pectoris
I25712Atherosclerosis of autologous vein coronary artery bypass graft(s) with refractory angina pectoris
I25722Atherosclerosis of autologous artery coronary artery bypass graft(s) with refractory angina pectoris
I25732Atherosclerosis of nonautologous biological coronary artery bypass graft(s) with refractory angina pectoris
I25752Atherosclerosis of native coronary artery of transplanted heart with refractory angina pectoris
I25762Atherosclerosis of bypass graft of coronary artery of transplanted heart with refractory angina pectoris
I25792Atherosclerosis of other coronary artery bypass graft(s) with refractory angina pectoris
I2585Chronic coronary microvascular dysfunction
I2589Other forms of chronic ischemic heart disease
I259Chronic ischemic heart disease, unspecified
I501Left ventricular failure, unspecified
I50810Right heart failure, unspecified
I50811Acute right heart failure
I50812Chronic right heart failure
I50813Acute on chronic right heart failure
I50814Right heart failure due to left heart failure
I5082Biventricular heart failure
I5083High output heart failure
I5084End stage heart failure
I5089Other heart failure
I509Heart failure, unspecified
I878Other specified disorders of veins
I879Disorder of vein, unspecified
I998Other disorder of circulatory system
I999Unspecified disorder of circulatory system
R570Cardiogenic shock
R579Shock, unspecified
 
PDX Collection 6987
A179Tuberculosis of nervous system, unspecified
A1810Tuberculosis of genitourinary system, unspecified
A1811Tuberculosis of kidney and ureter
A1813Tuberculosis of other urinary organs
A1882Tuberculosis of other endocrine glands
A1884Tuberculosis of heart
A1889Tuberculosis of other sites
A5421Gonococcal infection of kidney and ureter
A5429Other gonococcal genitourinary infections
A5482Gonococcal brain abscess
A5484Gonococcal pneumonia
A5489Other gonococcal infections
A549Gonococcal infection, unspecified
A5900Urogenital trichomoniasis, unspecified
A598Trichomoniasis of other sites
A599Trichomoniasis, unspecified
A985Hemorrhagic fever with renal syndrome
B3741Candidal cystitis and urethritis
B3742Candidal balanitis
B3749Other urogenital candidiasis
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
E09618Drug or chemical induced diabetes mellitus with other diabetic arthropathy
E09620Drug or chemical induced diabetes mellitus with diabetic dermatitis
E09621Drug or chemical induced diabetes mellitus with foot ulcer
E09622Drug or chemical induced diabetes mellitus with other skin ulcer
E09628Drug or chemical induced diabetes mellitus with other skin complications
E09630Drug or chemical induced diabetes mellitus with periodontal disease
E09638Drug or chemical induced diabetes mellitus with other oral complications
E09649Drug or chemical induced diabetes mellitus with hypoglycemia without coma
E0965Drug or chemical induced diabetes mellitus with hyperglycemia
E0969Drug or chemical induced diabetes mellitus with other specified complication
E098Drug or chemical induced diabetes mellitus with unspecified complications
E1021Type 1 diabetes mellitus with diabetic nephropathy
E1022Type 1 diabetes mellitus with diabetic chronic kidney disease
E1029Type 1 diabetes mellitus with other diabetic kidney complication
E10618Type 1 diabetes mellitus with other diabetic arthropathy
E10620Type 1 diabetes mellitus with diabetic dermatitis
E10621Type 1 diabetes mellitus with foot ulcer
E10622Type 1 diabetes mellitus with other skin ulcer
E10628Type 1 diabetes mellitus with other skin complications
E10630Type 1 diabetes mellitus with periodontal disease
E10638Type 1 diabetes mellitus with other oral complications
E10649Type 1 diabetes mellitus with hypoglycemia without coma
E1069Type 1 diabetes mellitus with other specified complication
E108Type 1 diabetes mellitus with unspecified complications
E1121Type 2 diabetes mellitus with diabetic nephropathy
E1122Type 2 diabetes mellitus with diabetic chronic kidney disease
E1129Type 2 diabetes mellitus with other diabetic kidney complication
E11618Type 2 diabetes mellitus with other diabetic arthropathy
E11620Type 2 diabetes mellitus with diabetic dermatitis
E11621Type 2 diabetes mellitus with foot ulcer
E11622Type 2 diabetes mellitus with other skin ulcer
E11628Type 2 diabetes mellitus with other skin complications
E11630Type 2 diabetes mellitus with periodontal disease
E11638Type 2 diabetes mellitus with other oral complications
E11649Type 2 diabetes mellitus with hypoglycemia without coma
E1169Type 2 diabetes mellitus with other specified complication
E118Type 2 diabetes mellitus with unspecified complications
E1321Other specified diabetes mellitus with diabetic nephropathy
E1322Other specified diabetes mellitus with diabetic chronic kidney disease
E1329Other specified diabetes mellitus with other diabetic kidney complication
E13618Other specified diabetes mellitus with other diabetic arthropathy
E13620Other specified diabetes mellitus with diabetic dermatitis
E13621Other specified diabetes mellitus with foot ulcer
E13622Other specified diabetes mellitus with other skin ulcer
E13628Other specified diabetes mellitus with other skin complications
E13630Other specified diabetes mellitus with periodontal disease
E13638Other specified diabetes mellitus with other oral complications
E13649Other specified diabetes mellitus with hypoglycemia without coma
E1365Other specified diabetes mellitus with hyperglycemia
E1369Other specified diabetes mellitus with other specified complication
E138Other specified diabetes mellitus with unspecified complications
M1030Gout due to renal impairment, unspecified site
M10311Gout due to renal impairment, right shoulder
M10312Gout due to renal impairment, left shoulder
M10319Gout due to renal impairment, unspecified shoulder
M10321Gout due to renal impairment, right elbow
M10322Gout due to renal impairment, left elbow
M10329Gout due to renal impairment, unspecified elbow
M10331Gout due to renal impairment, right wrist
M10332Gout due to renal impairment, left wrist
M10339Gout due to renal impairment, unspecified wrist
M10341Gout due to renal impairment, right hand
M10342Gout due to renal impairment, left hand
M10349Gout due to renal impairment, unspecified hand
M10351Gout due to renal impairment, right hip
M10352Gout due to renal impairment, left hip
M10359Gout due to renal impairment, unspecified hip
M10361Gout due to renal impairment, right knee
M10362Gout due to renal impairment, left knee
M10369Gout due to renal impairment, unspecified knee
M10371Gout due to renal impairment, right ankle and foot
M10372Gout due to renal impairment, left ankle and foot
M10379Gout due to renal impairment, unspecified ankle and foot
M1038Gout due to renal impairment, vertebrae



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13 Oct 2023 12:52:35
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