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

Previous Page [Alt-p] Up a level [Alt-u] Next Page [Alt-n]
Appendix C: Principal diagnoses which convert CC/MCC to non-CC
Page 1184 of 1324
 
PDX Collection 6492
I10Essential (primary) hypertension
I110Hypertensive heart disease with heart failure
I119Hypertensive heart disease without heart failure
I120Hypertensive chronic kidney disease with stage 5 chronic kidney disease or end stage renal disease
I129Hypertensive chronic kidney disease with stage 1 through stage 4 chronic kidney disease, or unspecified chronic kidney disease
I130Hypertensive heart and chronic kidney disease with heart failure and stage 1 through stage 4 chronic kidney disease, or unspecified chronic kidney disease
I1310Hypertensive heart and chronic kidney disease without heart failure, with stage 1 through stage 4 chronic kidney disease, or unspecified chronic kidney disease
I1311Hypertensive heart and chronic kidney disease without heart failure, with stage 5 chronic kidney disease, or end stage renal disease
I132Hypertensive heart and chronic kidney disease with heart failure and with stage 5 chronic kidney disease, or end stage renal disease
I150Renovascular hypertension
I151Hypertension secondary to other renal disorders
I152Hypertension secondary to endocrine disorders
I158Other secondary hypertension
I159Secondary hypertension, unspecified
I160Hypertensive urgency
I161Hypertensive emergency
I169Hypertensive crisis, unspecified
I1A0Resistant hypertension
I878Other specified disorders of veins
I879Disorder of vein, unspecified
I998Other disorder of circulatory system
I999Unspecified disorder of circulatory system
N262Page kidney
 
PDX Collection 6493
I440Atrioventricular block, first degree
I441Atrioventricular block, second degree
I442Atrioventricular block, complete
I4430Unspecified atrioventricular block
I4439Other atrioventricular block
I444Left anterior fascicular block
I445Left posterior fascicular block
I4460Unspecified fascicular block
I4469Other fascicular block
I447Left bundle-branch block, unspecified
I450Right fascicular block
I4510Unspecified right bundle-branch block
I4519Other right bundle-branch block
I452Bifascicular block
I453Trifascicular block
I454Nonspecific intraventricular block
I455Other specified heart block
I456Pre-excitation syndrome
I4581Long QT syndrome
I4589Other specified conduction disorders
I459Conduction disorder, unspecified
I469Cardiac arrest, cause unspecified
I470Re-entry ventricular arrhythmia
I4710Supraventricular tachycardia, unspecified
I4711Inappropriate sinus tachycardia, so stated
I4719Other supraventricular tachycardia
I4720Ventricular tachycardia, unspecified
I4721Torsades de pointes
I4729Other ventricular tachycardia
I479Paroxysmal tachycardia, unspecified
I480Paroxysmal atrial fibrillation
I4811Longstanding persistent atrial fibrillation
I4819Other persistent atrial fibrillation
I4820Chronic atrial fibrillation, unspecified
I4821Permanent atrial fibrillation
I483Typical atrial flutter
I484Atypical atrial flutter
I4891Unspecified atrial fibrillation
I4892Unspecified atrial flutter
I4901Ventricular fibrillation
I4902Ventricular flutter
I492Junctional premature depolarization
I498Other specified cardiac arrhythmias
I878Other specified disorders of veins
I879Disorder of vein, unspecified
I998Other disorder of circulatory system
I999Unspecified disorder of circulatory system
R001Bradycardia, unspecified
 
PDX Collection 6494
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
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
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
D693Immune thrombocytopenic purpura
D6941Evans syndrome
D6942Congenital and hereditary thrombocytopenia purpura
D6949Other primary thrombocytopenia
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 6495
I440Atrioventricular block, first degree
I441Atrioventricular block, second degree
I442Atrioventricular block, complete
I4430Unspecified atrioventricular block
I4439Other atrioventricular block
I444Left anterior fascicular block
I445Left posterior fascicular block
I4460Unspecified fascicular block
I4469Other fascicular block
I447Left bundle-branch block, unspecified
I450Right fascicular block
I4510Unspecified right bundle-branch block
I4519Other right bundle-branch block
I452Bifascicular block
I453Trifascicular block
I454Nonspecific intraventricular block
I455Other specified heart block
I456Pre-excitation syndrome
I4581Long QT syndrome
I4589Other specified conduction disorders
I459Conduction disorder, unspecified
I469Cardiac arrest, cause unspecified
I470Re-entry ventricular arrhythmia
I4710Supraventricular tachycardia, unspecified
I4711Inappropriate sinus tachycardia, so stated
I4719Other supraventricular tachycardia
I4720Ventricular tachycardia, unspecified
I4721Torsades de pointes
I4729Other ventricular tachycardia
I479Paroxysmal tachycardia, unspecified
I480Paroxysmal atrial fibrillation
I4811Longstanding persistent atrial fibrillation
I4819Other persistent atrial fibrillation
I4820Chronic atrial fibrillation, unspecified
I4821Permanent atrial fibrillation
I483Typical atrial flutter
I484Atypical atrial flutter
I4891Unspecified atrial fibrillation
I4892Unspecified atrial flutter
I4901Ventricular fibrillation
I4902Ventricular flutter
I492Junctional premature depolarization
I498Other specified cardiac arrhythmias
I878Other specified disorders of veins
I879Disorder of vein, unspecified
I998Other disorder of circulatory system
I999Unspecified disorder of circulatory system
R001Bradycardia, unspecified
 
PDX Collection 6496
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
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 6497
Q900Trisomy 21, nonmosaicism (meiotic nondisjunction)
Q901Trisomy 21, mosaicism (mitotic nondisjunction)
Q902Trisomy 21, translocation
Q909Down syndrome, unspecified
Q910Trisomy 18, nonmosaicism (meiotic nondisjunction)
Q911Trisomy 18, mosaicism (mitotic nondisjunction)
Q912Trisomy 18, translocation
Q913Trisomy 18, unspecified
Q914Trisomy 13, nonmosaicism (meiotic nondisjunction)
Q915Trisomy 13, mosaicism (mitotic nondisjunction)
Q916Trisomy 13, translocation
Q917Trisomy 13, unspecified
Q920Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction)
Q921Whole chromosome trisomy, mosaicism (mitotic nondisjunction)
Q922Partial trisomy
Q925Duplications with other complex rearrangements
Q9261Marker chromosomes in normal individual
Q9262Marker chromosomes in abnormal individual
Q927Triploidy and polyploidy
Q928Other specified trisomies and partial trisomies of autosomes
Q929Trisomy and partial trisomy of autosomes, unspecified
Q930Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction)
Q931Whole chromosome monosomy, mosaicism (mitotic nondisjunction)
Q932Chromosome replaced with ring, dicentric or isochromosome
Q933Deletion of short arm of chromosome 4
Q934Deletion of short arm of chromosome 5
Q9351Angelman syndrome
Q9352Phelan-McDermid syndrome
Q9359Other deletions of part of a chromosome
Q937Deletions with other complex rearrangements
Q9381Velo-cardio-facial syndrome
Q9382Williams syndrome
Q9388Other microdeletions
Q9389Other deletions from the autosomes
Q939Deletion from autosomes, unspecified
Q950Balanced translocation and insertion in normal individual
Q951Chromosome inversion in normal individual
Q952Balanced autosomal rearrangement in abnormal individual
Q953Balanced sex/autosomal rearrangement in abnormal individual
Q955Individual with autosomal fragile site
Q958Other balanced rearrangements and structural markers
Q959Balanced rearrangement and structural marker, unspecified
Q960Karyotype 45, X
Q961Karyotype 46, X iso (Xq)
Q962Karyotype 46, X with abnormal sex chromosome, except iso (Xq)
Q963Mosaicism, 45, X/46, XX or XY
Q964Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome
Q968Other variants of Turner's syndrome
Q969Turner's syndrome, unspecified
Q970Karyotype 47, XXX
Q971Female with more than three X chromosomes
Q972Mosaicism, lines with various numbers of X chromosomes
Q973Female with 46, XY karyotype
Q978Other specified sex chromosome abnormalities, female phenotype
Q979Sex chromosome abnormality, female phenotype, unspecified
Q980Klinefelter syndrome karyotype 47, XXY
Q981Klinefelter syndrome, male with more than two X chromosomes
Q983Other male with 46, XX karyotype
Q984Klinefelter syndrome, unspecified
Q985Karyotype 47, XYY
Q986Male with structurally abnormal sex chromosome
Q987Male with sex chromosome mosaicism
Q988Other specified sex chromosome abnormalities, male phenotype
Q989Sex chromosome abnormality, male phenotype, unspecified
Q990Chimera 46, XX/46, XY
Q99146, XX true hermaphrodite
Q998Other specified chromosome abnormalities
Q999Chromosomal abnormality, unspecified
 
PDX Collection 6498
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



Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244
13 Oct 2023 12:52:35
CMS, code-revision=349, description-revision=1375