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 1133 of 1324
PDX Collection 6270 (continued)
D57439Sickle-cell thalassemia beta zero with crisis, unspecified
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
D5930Hemolytic-uremic syndrome, unspecified
D5931Infection-associated hemolytic-uremic syndrome
D5932Hereditary hemolytic-uremic syndrome
D5939Other hemolytic-uremic syndrome
 
PDX Collection 6271
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 6272
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
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 6273
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
H49811Kearns-Sayre syndrome, right eye
 
PDX Collection 6274
G40001Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, with status epilepticus
G40009Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, without status epilepticus
G40011Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, with status epilepticus
G40019Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, without status epilepticus
G40101Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, with status epilepticus
G40109Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, without status epilepticus
G40111Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, with status epilepticus
G40119Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, without status epilepticus
G40201Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, with status epilepticus
G40209Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, without status epilepticus
G40211Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, with status epilepticus
G40219Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, without status epilepticus
G40301Generalized idiopathic epilepsy and epileptic syndromes, not intractable, with status epilepticus
G40309Generalized idiopathic epilepsy and epileptic syndromes, not intractable, without status epilepticus
G40311Generalized idiopathic epilepsy and epileptic syndromes, intractable, with status epilepticus
G40319Generalized idiopathic epilepsy and epileptic syndromes, intractable, without status epilepticus
G40401Other generalized epilepsy and epileptic syndromes, not intractable, with status epilepticus
G40409Other generalized epilepsy and epileptic syndromes, not intractable, without status epilepticus
G40411Other generalized epilepsy and epileptic syndromes, intractable, with status epilepticus
G40419Other generalized epilepsy and epileptic syndromes, intractable, without status epilepticus
G4042Cyclin-Dependent Kinase-Like 5 Deficiency Disorder
G40501Epileptic seizures related to external causes, not intractable, with status epilepticus
G40509Epileptic seizures related to external causes, not intractable, without status epilepticus
G40801Other epilepsy, not intractable, with status epilepticus
G40802Other epilepsy, not intractable, without status epilepticus
G40803Other epilepsy, intractable, with status epilepticus
G40804Other epilepsy, intractable, without status epilepticus
G40811Lennox-Gastaut syndrome, not intractable, with status epilepticus
G40812Lennox-Gastaut syndrome, not intractable, without status epilepticus
G40813Lennox-Gastaut syndrome, intractable, with status epilepticus
G40814Lennox-Gastaut syndrome, intractable, without status epilepticus
G40821Epileptic spasms, not intractable, with status epilepticus
G40822Epileptic spasms, not intractable, without status epilepticus
G40823Epileptic spasms, intractable, with status epilepticus
G40824Epileptic spasms, intractable, without status epilepticus
G40833Dravet syndrome, intractable, with status epilepticus
G40834Dravet syndrome, intractable, without status epilepticus
G4089Other seizures
G40901Epilepsy, unspecified, not intractable, with status epilepticus
G40909Epilepsy, unspecified, not intractable, without status epilepticus
G40911Epilepsy, unspecified, intractable, with status epilepticus
G40919Epilepsy, unspecified, intractable, without status epilepticus
G40A01Absence epileptic syndrome, not intractable, with status epilepticus
G40A09Absence epileptic syndrome, not intractable, without status epilepticus
G40A11Absence epileptic syndrome, intractable, with status epilepticus
G40A19Absence epileptic syndrome, intractable, without status epilepticus
G40B01Juvenile myoclonic epilepsy, not intractable, with status epilepticus
G40B09Juvenile myoclonic epilepsy, not intractable, without status epilepticus
G40B11Juvenile myoclonic epilepsy, intractable, with status epilepticus
G40B19Juvenile myoclonic epilepsy, intractable, without status epilepticus
G40C01Lafora progressive myoclonus epilepsy, not intractable, with status epilepticus
G40C09Lafora progressive myoclonus epilepsy, not intractable, without status epilepticus
G40C11Lafora progressive myoclonus epilepsy, intractable, with status epilepticus
G40C19Lafora progressive myoclonus epilepsy, intractable, without status epilepticus
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9342Megaloencephalic leukoencephalopathy with subcortical cysts
G9343Leukoencephalopathy with calcifications and cysts
G9344Adult-onset leukodystrophy with axonal spheroids
G9349Other encephalopathy
G939Disorder of brain, unspecified
G969Disorder of central nervous system, unspecified
G980Neurogenic arthritis, not elsewhere classified
G988Other disorders of nervous system
I6783Posterior reversible encephalopathy syndrome
R561Post traumatic seizures
 
PDX Collection 6275
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 6276
A150Tuberculosis of lung
A154Tuberculosis of intrathoracic lymph nodes
A155Tuberculosis of larynx, trachea and bronchus
A156Tuberculous pleurisy
A158Other respiratory tuberculosis
A159Respiratory tuberculosis unspecified
A179Tuberculosis of nervous system, unspecified
A1882Tuberculosis of other endocrine glands
A1884Tuberculosis of heart
A1889Tuberculosis of other sites
A212Pulmonary tularemia
A221Pulmonary anthrax
A310Pulmonary mycobacterial infection
A3701Whooping cough due to Bordetella pertussis with pneumonia
A3711Whooping cough due to Bordetella parapertussis with pneumonia
A3781Whooping cough due to other Bordetella species with pneumonia
A3791Whooping cough, unspecified species with pneumonia
A420Pulmonary actinomycosis
A430Pulmonary nocardiosis
A481Legionnaires' disease
B250Cytomegaloviral pneumonitis
B390Acute pulmonary histoplasmosis capsulati
B391Chronic pulmonary histoplasmosis capsulati
B392Pulmonary histoplasmosis capsulati, unspecified
B440Invasive pulmonary aspergillosis
B583Pulmonary toxoplasmosis
B59Pneumocystosis
B671Echinococcus granulosus infection of lung
J09X1Influenza due to identified novel influenza A virus with pneumonia
J09X2Influenza due to identified novel influenza A virus with other respiratory manifestations
J1000Influenza due to other identified influenza virus with unspecified type of pneumonia
J1001Influenza due to other identified influenza virus with the same other identified influenza virus pneumonia
J1008Influenza due to other identified influenza virus with other specified pneumonia
J101Influenza due to other identified influenza virus with other respiratory manifestations
J1100Influenza due to unidentified influenza virus with unspecified type of pneumonia
J1108Influenza due to unidentified influenza virus with specified pneumonia
J111Influenza due to unidentified influenza virus with other respiratory manifestations
J120Adenoviral pneumonia
J121Respiratory syncytial virus pneumonia
J122Parainfluenza virus pneumonia
J123Human metapneumovirus pneumonia
J1289Other viral pneumonia
J129Viral pneumonia, unspecified
J13Pneumonia due to Streptococcus pneumoniae
J14Pneumonia due to Hemophilus influenzae
J150Pneumonia due to Klebsiella pneumoniae
J151Pneumonia due to Pseudomonas
J1520Pneumonia due to staphylococcus, unspecified
J15211Pneumonia due to Methicillin susceptible Staphylococcus aureus
J15212Pneumonia due to Methicillin resistant Staphylococcus aureus
J1529Pneumonia due to other staphylococcus
J153Pneumonia due to streptococcus, group B
J154Pneumonia due to other streptococci
J155Pneumonia due to Escherichia coli
J1561Pneumonia due to Acinetobacter baumannii
J1569Pneumonia due to other Gram-negative bacteria
J157Pneumonia due to Mycoplasma pneumoniae
J158Pneumonia due to other specified bacteria
J159Unspecified bacterial pneumonia
J160Chlamydial pneumonia
J168Pneumonia due to other specified infectious organisms
J180Bronchopneumonia, unspecified organism
J181Lobar pneumonia, unspecified organism
J188Other pneumonia, unspecified organism
J189Pneumonia, unspecified organism
J22Unspecified acute lower respiratory infection
J4481Bronchiolitis obliterans and bronchiolitis obliterans syndrome
J4489Other specified chronic obstructive pulmonary disease
J449Chronic obstructive pulmonary disease, unspecified
J470Bronchiectasis with acute lower respiratory infection
J471Bronchiectasis with (acute) exacerbation
J479Bronchiectasis, uncomplicated
J4A0Restrictive allograft syndrome
J4A8Other chronic lung allograft dysfunction
J4A9Chronic lung allograft dysfunction, unspecified
J60Coalworker's pneumoconiosis
J61Pneumoconiosis due to asbestos and other mineral fibers
J620Pneumoconiosis due to talc dust
J628Pneumoconiosis due to other dust containing silica
J630Aluminosis (of lung)
J631Bauxite fibrosis (of lung)
J632Berylliosis
J633Graphite fibrosis (of lung)
J634Siderosis
J635Stannosis
J636Pneumoconiosis due to other specified inorganic dusts
J64Unspecified pneumoconiosis
J65Pneumoconiosis associated with tuberculosis
J660Byssinosis
J661Flax-dressers' disease
J662Cannabinosis
J668Airway disease due to other specific organic dusts
J670Farmer's lung
J671Bagassosis
J672Bird fancier's lung
J673Suberosis
J674Maltworker's lung
J675Mushroom-worker's lung



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13 Oct 2023 12:52:35
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