DRAFT

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

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Part 1: List of CC and Major CC codes
Page 5 of 46
A000 A8183 C229 C8292 D613 F0394 G40823 H5988 I70368 J157 K7111 L97526 M4857XA M84477A M8669 N184 O364XX1 P3610 R402211 S0633AA S13101A S25309A S32434K S37022A S42309P S45012A S52101Q S52261C S52363B S52611P S62031P S62344K S65311A S72065C S72324Q S72431K S76829A S82109M S82232A S82435Q S82856M S89321K S92341P T24322A T81506A T85694A
DxCC/MCCExclusionsDescription
D613MCC 6297:115 codesIdiopathic aplastic anemia
D61810MCC 0500:45 codesAntineoplastic chemotherapy induced pancytopenia
D61811MCC 0500:45 codesOther drug-induced pancytopenia
D61818CC 0500:45 codesOther pancytopenia
D6182CC 0500:45 codesMyelophthisis
D6189MCC 6364:115 codesOther specified aplastic anemias and other bone marrow failure syndromes
D619CC 6294:115 codesAplastic anemia, unspecified
D62CC 6771:116 codesAcute posthemorrhagic anemia
D65MCC 5564:52 codesDisseminated intravascular coagulation [defibrination syndrome]
D66MCC 5566:52 codesHereditary factor VIII deficiency
D67MCC 5565:52 codesHereditary factor IX deficiency
D6800CC 4847:51 codesVon Willebrand disease, unspecified
D6801CC 4846:51 codesVon Willebrand disease, type 1
D68020CC 4937:51 codesVon Willebrand disease, type 2A
D68021CC 4939:51 codesVon Willebrand disease, type 2B
D68022CC 4940:51 codesVon Willebrand disease, type 2M
D68023CC 4943:51 codesVon Willebrand disease, type 2N
D68029CC 4930:51 codesVon Willebrand disease, type 2, unspecified
D6803CC 4856:51 codesVon Willebrand disease, type 3
D6804CC 4854:51 codesAcquired von Willebrand disease
D6809CC 4853:51 codesOther von Willebrand disease
D681CC 5158:52 codesHereditary factor XI deficiency
D682CC 5155:52 codesHereditary deficiency of other clotting factors
D68311CC 5745:51 codesAcquired hemophilia
D68312CC 5746:52 codesAntiphospholipid antibody with hemorrhagic disorder
D68318CC 5739:51 codesOther hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
D6832CC 4820:52 codesHemorrhagic disorder due to extrinsic circulating anticoagulants
D684CC 5151:52 codesAcquired coagulation factor deficiency
D6851CC 0505:40 codesActivated protein C resistance
D6852CC 0505:40 codesProthrombin gene mutation
D6859CC 4371:42 codesOther primary thrombophilia
D6861CC 0505:40 codesAntiphospholipid syndrome
D6862CC 0505:40 codesLupus anticoagulant syndrome
D6869CC 4372:42 codesOther thrombophilia
D688CC 5149:52 codesOther specified coagulation defects
D689CC 5146:52 codesCoagulation defect, unspecified
D690CC 5182:52 codesAllergic purpura
D693CC 5177:54 codesImmune thrombocytopenic purpura
D6941CC 5455:54 codesEvans syndrome
D6942CC 5454:54 codesCongenital and hereditary thrombocytopenia purpura
D740CC 0506:24 codesCongenital methemoglobinemia
D748CC 0506:24 codesOther methemoglobinemias
D749CC 0506:24 codesMethemoglobinemia, unspecified
D7581CC 3619:130 codesMyelofibrosis
D761CC 5673:39 codesHemophagocytic lymphohistiocytosis
D762CC 5672:39 codesHemophagocytic syndrome, infection-associated
D763CC 5671:39 codesOther histiocytosis syndromes
D7801CC 0508:80 codesIntraoperative hemorrhage and hematoma of the spleen complicating a procedure on the spleen
D7802CC 0508:80 codesIntraoperative hemorrhage and hematoma of the spleen complicating other procedure
D7811CC 0509:76 codesAccidental puncture and laceration of the spleen during a procedure on the spleen
D7812CC 0509:76 codesAccidental puncture and laceration of the spleen during other procedure
D7821CC 0508:80 codesPostprocedural hemorrhage of the spleen following a procedure on the spleen
D7822CC 0508:80 codesPostprocedural hemorrhage of the spleen following other procedure
D7831CC 0508:80 codesPostprocedural hematoma of the spleen following a procedure on the spleen
D7832CC 0508:80 codesPostprocedural hematoma of the spleen following other procedure
D7833CC 0508:80 codesPostprocedural seroma of the spleen following a procedure on the spleen
D7834CC 0508:80 codesPostprocedural seroma of the spleen following other procedure
D7881CC 0510:18 codesOther intraoperative complications of the spleen
D7889CC 0510:18 codesOther postprocedural complications of the spleen
D800CC 6225:45 codesHereditary hypogammaglobulinemia
D801CC 6223:47 codesNonfamilial hypogammaglobulinemia
D802CC 6222:47 codesSelective deficiency of immunoglobulin A [IgA]
D803CC 6221:45 codesSelective deficiency of immunoglobulin G [IgG] subclasses
D804CC 6218:45 codesSelective deficiency of immunoglobulin M [IgM]
D805CC 6216:45 codesImmunodeficiency with increased immunoglobulin M [IgM]
D806CC 6215:45 codesAntibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
D807CC 6213:45 codesTransient hypogammaglobulinemia of infancy
D808CC 6212:45 codesOther immunodeficiencies with predominantly antibody defects
D809CC 6210:45 codesImmunodeficiency with predominantly antibody defects, unspecified
D810CC 6246:45 codesSevere combined immunodeficiency [SCID] with reticular dysgenesis
D811CC 6245:45 codesSevere combined immunodeficiency [SCID] with low T- and B-cell numbers
D812CC 6242:45 codesSevere combined immunodeficiency [SCID] with low or normal B-cell numbers
D8130CC 6357:35 codesAdenosine deaminase deficiency, unspecified
D8131CC 6358:35 codesSevere combined immunodeficiency due to adenosine deaminase deficiency
D8132CC 6359:35 codesAdenosine deaminase 2 deficiency
D8139CC 6387:35 codesOther adenosine deaminase deficiency
D814CC 6240:45 codesNezelof's syndrome
D815CC 6238:35 codesPurine nucleoside phosphorylase [PNP] deficiency
D816CC 6237:45 codesMajor histocompatibility complex class I deficiency
D817CC 6233:45 codesMajor histocompatibility complex class II deficiency
D8182CC 6320:45 codesActivated Phosphoinositide 3-kinase Delta Syndrome [APDS]
D8189CC 6312:45 codesOther combined immunodeficiencies
D819CC 6231:45 codesCombined immunodeficiency, unspecified
D820CC 6259:45 codesWiskott-Aldrich syndrome
D821CC 6258:45 codesDi George's syndrome
D830CC 6282:45 codesCommon variable immunodeficiency with predominant abnormalities of B-cell numbers and function
D831CC 6281:45 codesCommon variable immunodeficiency with predominant immunoregulatory T-cell disorders
D832CC 6280:45 codesCommon variable immunodeficiency with autoantibodies to B- or T-cells
D838CC 6277:45 codesOther common variable immunodeficiencies
D839CC 6275:45 codesCommon variable immunodeficiency, unspecified
D8481CC 6860:45 codesImmunodeficiency due to conditions classified elsewhere
D84821CC 6689:45 codesImmunodeficiency due to drugs
D84822CC 6700:45 codesImmunodeficiency due to external causes
D8489CC 6824:45 codesOther immunodeficiencies
D849CC 6287:45 codesImmunodeficiency, unspecified
D89810CC 0514:49 codesAcute graft-versus-host disease
D89811CC 0514:49 codesChronic graft-versus-host disease
D89812CC 0514:49 codesAcute on chronic graft-versus-host disease
D89813CC 0514:49 codesGraft-versus-host disease, unspecified
D89833CC 4123:6 codesCytokine release syndrome, grade 3
D89834CC 4123:6 codesCytokine release syndrome, grade 4
D89835CC 4123:6 codesCytokine release syndrome, grade 5
E035MCC 4654:878 codesMyxedema coma
E0501MCC 0516:60 codesThyrotoxicosis with diffuse goiter with thyrotoxic crisis or storm
E0511MCC 0516:60 codesThyrotoxicosis with toxic single thyroid nodule with thyrotoxic crisis or storm
E0521MCC 0516:60 codesThyrotoxicosis with toxic multinodular goiter with thyrotoxic crisis or storm
E0531MCC 0516:60 codesThyrotoxicosis from ectopic thyroid tissue with thyrotoxic crisis or storm
E0541MCC 0516:60 codesThyrotoxicosis factitia with thyrotoxic crisis or storm
E0581MCC 0516:60 codesOther thyrotoxicosis with thyrotoxic crisis or storm
E0591MCC 0516:60 codesThyrotoxicosis, unspecified with thyrotoxic crisis or storm
E060CC 0517:7 codesAcute thyroiditis
E0800MCC 0518:431 codesDiabetes mellitus due to underlying condition with hyperosmolarity without nonketotic hyperglycemic-hyperosmolar coma (NKHHC)
E0801MCC 0518:431 codesDiabetes mellitus due to underlying condition with hyperosmolarity with coma
E0810MCC 0518:431 codesDiabetes mellitus due to underlying condition with ketoacidosis without coma
E0811MCC 0518:431 codesDiabetes mellitus due to underlying condition with ketoacidosis with coma
E0852CC 3626:91 codesDiabetes mellitus due to underlying condition with diabetic peripheral angiopathy with gangrene
E08641MCC 0518:431 codesDiabetes mellitus due to underlying condition with hypoglycemia with coma
E0900MCC 0518:431 codesDrug or chemical induced diabetes mellitus with hyperosmolarity without nonketotic hyperglycemic-hyperosmolar coma (NKHHC)
E0901MCC 0518:431 codesDrug or chemical induced diabetes mellitus with hyperosmolarity with coma
E0910MCC 0518:431 codesDrug or chemical induced diabetes mellitus with ketoacidosis without coma
E0911MCC 0518:431 codesDrug or chemical induced diabetes mellitus with ketoacidosis with coma
E0952CC 3628:91 codesDrug or chemical induced diabetes mellitus with diabetic peripheral angiopathy with gangrene
E09641MCC 0518:431 codesDrug or chemical induced diabetes mellitus with hypoglycemia with coma
E1010MCC 0520:434 codesType 1 diabetes mellitus with ketoacidosis without coma
E1011MCC 0520:434 codesType 1 diabetes mellitus with ketoacidosis with coma
E1052CC 3630:91 codesType 1 diabetes mellitus with diabetic peripheral angiopathy with gangrene
E10641MCC 0520:434 codesType 1 diabetes mellitus with hypoglycemia with coma
E1100MCC 0518:431 codesType 2 diabetes mellitus with hyperosmolarity without nonketotic hyperglycemic-hyperosmolar coma (NKHHC)
E1101MCC 0518:431 codesType 2 diabetes mellitus with hyperosmolarity with coma
E1110MCC 0518:431 codesType 2 diabetes mellitus with ketoacidosis without coma
E1111MCC 0518:431 codesType 2 diabetes mellitus with ketoacidosis with coma
E1152CC 3632:91 codesType 2 diabetes mellitus with diabetic peripheral angiopathy with gangrene
E11641MCC 0518:431 codesType 2 diabetes mellitus with hypoglycemia with coma
E1300MCC 0518:431 codesOther specified diabetes mellitus with hyperosmolarity without nonketotic hyperglycemic-hyperosmolar coma (NKHHC)
E1301MCC 0518:431 codesOther specified diabetes mellitus with hyperosmolarity with coma
E1310MCC 0518:431 codesOther specified diabetes mellitus with ketoacidosis without coma
E1311MCC 0518:431 codesOther specified diabetes mellitus with ketoacidosis with coma
E1352CC 3634:91 codesOther specified diabetes mellitus with diabetic peripheral angiopathy with gangrene
E13641MCC 0518:431 codesOther specified diabetes mellitus with hypoglycemia with coma
E15CC 0520:434 codesNondiabetic hypoglycemic coma
E221CC 0521:4 codesHyperprolactinemia
E222CC 0522:19 codesSyndrome of inappropriate secretion of antidiuretic hormone
E228CC 0521:4 codesOther hyperfunction of pituitary gland
E229CC 0521:4 codesHyperfunction of pituitary gland, unspecified
E230CC 0523:22 codesHypopituitarism
E232CC 0524:20 codesDiabetes insipidus
E240CC 0525:24 codesPituitary-dependent Cushing's disease
E242CC 0525:24 codesDrug-induced Cushing's syndrome
E243CC 0525:24 codesEctopic ACTH syndrome
E244CC 0525:24 codesAlcohol-induced pseudo-Cushing's syndrome
E248CC 0525:24 codesOther Cushing's syndrome
E249CC 0525:24 codesCushing's syndrome, unspecified
E270CC 0526:23 codesOther adrenocortical overactivity
E271CC 0526:23 codesPrimary adrenocortical insufficiency
E272CC 0526:23 codesAddisonian crisis
E273CC 0526:23 codesDrug-induced adrenocortical insufficiency
E2740CC 0526:23 codesUnspecified adrenocortical insufficiency
E2749CC 0526:23 codesOther adrenocortical insufficiency
E275CC 0526:23 codesAdrenomedullary hyperfunction
E321CC 0527:12 codesAbscess of thymus
E340CC 0528:10 codesCarcinoid syndrome
E3601CC 0529:80 codesIntraoperative hemorrhage and hematoma of an endocrine system organ or structure complicating an endocrine system procedure
E3602CC 0529:80 codesIntraoperative hemorrhage and hematoma of an endocrine system organ or structure complicating other procedure
E3611CC 0509:76 codesAccidental puncture and laceration of an endocrine system organ or structure during an endocrine system procedure
E3612CC 0509:76 codesAccidental puncture and laceration of an endocrine system organ or structure during other procedure
E40MCC 0530:9 codesKwashiorkor
E41MCC 0530:9 codesNutritional marasmus
E42MCC 0530:9 codesMarasmic kwashiorkor
E43MCC 0530:9 codesUnspecified severe protein-calorie malnutrition
E440CC 0530:9 codesModerate protein-calorie malnutrition
E441CC 0530:9 codesMild protein-calorie malnutrition
E45CC 0530:9 codesRetarded development following protein-calorie malnutrition
E46CC 0530:9 codesUnspecified protein-calorie malnutrition
E5111CC 0531:34 codesDry beriberi
E5112CC 0531:34 codesWet beriberi
E512CC 0531:34 codesWernicke's encephalopathy
E518CC 0531:34 codesOther manifestations of thiamine deficiency
E519CC 0531:34 codesThiamine deficiency, unspecified
E530CC 0531:34 codesRiboflavin deficiency
E550CC 0532:34 codesRickets, active
E640CC 0530:9 codesSequelae of protein-calorie malnutrition
E662CC 0533:13 codesMorbid (severe) obesity with alveolar hypoventilation
E700CC 6326:127 codesClassical phenylketonuria
E701CC 6327:127 codesOther hyperphenylalaninemias
E7020CC 6478:127 codesDisorder of tyrosine metabolism, unspecified
E7021CC 6479:127 codesTyrosinemia
E7029CC 6445:127 codesOther disorders of tyrosine metabolism
E7030CC 6460:127 codesAlbinism, unspecified
E70310CC 6791:127 codesX-linked ocular albinism
E70311CC 6792:127 codesAutosomal recessive ocular albinism
E70318CC 6788:127 codesOther ocular albinism
E70319CC 6789:127 codesOcular albinism, unspecified
E70320CC 6996:127 codesTyrosinase negative oculocutaneous albinism
E70321CC 6992:127 codesTyrosinase positive oculocutaneous albinism
E70328CC 6991:127 codesOther oculocutaneous albinism
E70329CC 6985:127 codesOculocutaneous albinism, unspecified
E70330CC 7017:127 codesChediak-Higashi syndrome
E70331CC 7018:127 codesHermansky-Pudlak syndrome
E70338CC 7012:127 codesOther albinism with hematologic abnormality
E70339CC 7014:127 codesAlbinism with hematologic abnormality, unspecified
E7039CC 6429:127 codesOther specified albinism
E7040CC 6442:127 codesDisorders of histidine metabolism, unspecified
E7041CC 6443:127 codesHistidinemia
E7049CC 6414:127 codesOther disorders of histidine metabolism
E705CC 6331:127 codesDisorders of tryptophan metabolism
E7081CC 4045:6 codesAromatic L-amino acid decarboxylase deficiency
E7089CC 4045:6 codesOther disorders of aromatic amino-acid metabolism
E709CC 6332:127 codesDisorder of aromatic amino-acid metabolism, unspecified
E710CC 6303:127 codesMaple-syrup-urine disease
E71110CC 6421:127 codesIsovaleric acidemia
E71111CC 6422:127 codes3-methylglutaconic aciduria
E71118CC 6415:127 codesOther branched-chain organic acidurias
E71120CC 6433:127 codesMethylmalonic acidemia
E71121CC 6434:127 codesPropionic acidemia
E71128CC 6430:127 codesOther disorders of propionate metabolism
E7119CC 6959:127 codesOther disorders of branched-chain amino-acid metabolism
E712CC 6304:127 codesDisorder of branched-chain amino-acid metabolism, unspecified
E71310CC 6491:38 codesLong chain/very long chain acyl CoA dehydrogenase deficiency
E71311CC 6487:38 codesMedium chain acyl CoA dehydrogenase deficiency
E71312CC 6488:38 codesShort chain acyl CoA dehydrogenase deficiency
E71313CC 6489:38 codesGlutaric aciduria type II
E71314CC 6490:38 codesMuscle carnitine palmitoyltransferase deficiency
E71318CC 6486:38 codesOther disorders of fatty-acid oxidation
E7132CC 6954:38 codesDisorders of ketone metabolism
E7139CC 6927:41 codesOther disorders of fatty-acid metabolism
E7150CC 6923:35 codesPeroxisomal disorder, unspecified
E71510CC 6295:35 codesZellweger syndrome
E71511CC 6296:35 codesNeonatal adrenoleukodystrophy
E71518CC 6292:35 codesOther disorders of peroxisome biogenesis
E71520CC 6314:35 codesChildhood cerebral X-linked adrenoleukodystrophy
E71521CC 6316:35 codesAdolescent X-linked adrenoleukodystrophy
E71522CC 6318:35 codesAdrenomyeloneuropathy
E71528CC 6305:35 codesOther X-linked adrenoleukodystrophy
E71529CC 6307:35 codesX-linked adrenoleukodystrophy, unspecified type
E7153CC 6921:35 codesOther group 2 peroxisomal disorders
E71540CC 6559:35 codesRhizomelic chondrodysplasia punctata
E71541CC 6560:35 codesZellweger-like syndrome
E71542CC 6553:35 codesOther group 3 peroxisomal disorders
E71548CC 6546:35 codesOther peroxisomal disorders
E7200CC 6579:127 codesDisorders of amino-acid transport, unspecified
E7201CC 6580:127 codesCystinuria
E7202CC 6576:127 codesHartnup's disease
E7203CC 3214:1 codeLowe's syndrome
E7204CC 6575:127 codesCystinosis
E7209CC 6585:127 codesOther disorders of amino-acid transport
E7210CC 6590:127 codesDisorders of sulfur-bearing amino-acid metabolism, unspecified
E7211CC 6545:127 codesHomocystinuria
E7212CC 6550:127 codesMethylenetetrahydrofolate reductase deficiency
E7219CC 6558:127 codesOther disorders of sulfur-bearing amino-acid metabolism
E7220CC 6571:127 codesDisorder of urea cycle metabolism, unspecified
E7221CC 6572:127 codesArgininemia
E7222CC 6526:127 codesArginosuccinic aciduria
E7223CC 6528:127 codesCitrullinemia
E7229CC 6522:127 codesOther disorders of urea cycle metabolism
E723CC 6350:127 codesDisorders of lysine and hydroxylysine metabolism
E724CC 6351:127 codesDisorders of ornithine metabolism
E7250CC 6507:127 codesDisorder of glycine metabolism, unspecified
E7251CC 6502:127 codesNon-ketotic hyperglycinemia
E7252CC 6506:127 codesTrimethylaminuria
E7253CC 6498:127 codesPrimary hyperoxaluria
E7259CC 6467:127 codesOther disorders of glycine metabolism
E7281CC 6444:127 codesDisorders of gamma aminobutyric acid metabolism
E7289CC 6417:127 codesOther specified disorders of amino-acid metabolism
E729CC 6354:127 codesDisorder of amino-acid metabolism, unspecified
E7400CC 6646:127 codesGlycogen storage disease, unspecified
E7401CC 6648:127 codesvon Gierke disease
E7402CC 6644:127 codesPompe disease
E7403CC 6645:127 codesCori disease
E7404CC 6642:127 codesMcArdle disease
E7405CC 6643:124 codesLysosome-associated membrane protein 2 [LAMP2] deficiency
E7409CC 6656:127 codesOther glycogen storage disease
E7420CC 6619:127 codesDisorders of galactose metabolism, unspecified
E7421CC 6620:127 codesGalactosemia
E7429CC 6628:127 codesOther disorders of galactose metabolism
E744CC 6376:127 codesDisorders of pyruvate metabolism and gluconeogenesis
E74810CC 6552:51 codesGlucose transporter protein type 1 deficiency
E74818CC 6533:51 codesOther disorders of glucose transport
E74819CC 6540:51 codesDisorders of glucose transport, unspecified
E7489CC 6484:51 codesOther specified disorders of carbohydrate metabolism
E7500CC 6153:29 codesGM2 gangliosidosis, unspecified
E7501CC 6151:29 codesSandhoff disease
E7502CC 6152:29 codesTay-Sachs disease
E7509CC 6158:29 codesOther GM2 gangliosidosis
E7510CC 6128:29 codesUnspecified gangliosidosis
E7511CC 6130:29 codesMucolipidosis IV
E7519CC 6139:29 codesOther gangliosidosis
E7523CC 6113:30 codesKrabbe disease
E7525CC 6111:30 codesMetachromatic leukodystrophy
E7526CC 6112:30 codesSulfatase deficiency
E7527CC 6119:24 codesPelizaeus-Merzbacher disease
E7528CC 6122:24 codesCanavan disease
E7529CC 6115:30 codesOther sphingolipidosis
E754CC 6362:29 codesNeuronal ceroid lipofuscinosis
E7601CC 6695:37 codesHurler's syndrome
E7602CC 6690:37 codesHurler-Scheie syndrome
E7603CC 6693:37 codesScheie's syndrome
E761CC 6403:37 codesMucopolysaccharidosis, type II
E76210CC 6756:37 codesMorquio A mucopolysaccharidoses
E76211CC 6755:37 codesMorquio B mucopolysaccharidoses
E76219CC 6750:37 codesMorquio mucopolysaccharidoses, unspecified
E7622CC 6680:37 codesSanfilippo mucopolysaccharidoses
E7629CC 6681:37 codesOther mucopolysaccharidoses
E763CC 6405:37 codesMucopolysaccharidosis, unspecified
E768CC 6407:37 codesOther disorders of glucosaminoglycan metabolism
E769CC 6408:37 codesGlucosaminoglycan metabolism disorder, unspecified
E7871CC 6670:20 codesBarth syndrome
E7872CC 6672:20 codesSmith-Lemli-Opitz syndrome
E791CC 6419:35 codesLesch-Nyhan syndrome
E792CC 6420:35 codesMyoadenylate deaminase deficiency
E7981CC 6154:35 codesAicardi-Goutières syndrome
E7982CC 6155:35 codesHereditary xanthinuria
E7989CC 6161:35 codesOther specified disorders of purine and pyrimidine metabolism
E799CC 6424:35 codesDisorder of purine and pyrimidine metabolism, unspecified
E800CC 6766:35 codesHereditary erythropoietic porphyria
E801CC 6768:35 codesPorphyria cutanea tarda
E8020CC 6897:35 codesUnspecified porphyria
E8021CC 6896:35 codesAcute intermittent (hepatic) porphyria
E8029CC 6862:35 codesOther porphyria
E803CC 6769:41 codesDefects of catalase and peroxidase
E840MCC 0541:5 codesCystic fibrosis with pulmonary manifestations
E8411MCC 0541:5 codesMeconium ileus in cystic fibrosis
E8419CC 0541:5 codesCystic fibrosis with other intestinal manifestations
E848CC 0541:5 codesCystic fibrosis with other manifestations
E849CC 0541:5 codesCystic fibrosis, unspecified
E850CC 6799:10 codesNon-neuropathic heredofamilial amyloidosis
E851CC 6800:10 codesNeuropathic heredofamilial amyloidosis
E852CC 6801:10 codesHeredofamilial amyloidosis, unspecified
E853CC 6803:10 codesSecondary systemic amyloidosis
E854CC 6804:10 codesOrgan-limited amyloidosis
E8581CC 6508:10 codesLight chain (AL) amyloidosis
E8582CC 6503:10 codesWild-type transthyretin-related (ATTR) amyloidosis
E8589CC 6472:10 codesOther amyloidosis
E859CC 6806:10 codesAmyloidosis, unspecified
E870CC 5690:17 codesHyperosmolality and hypernatremia
E871CC 5691:17 codesHypo-osmolality and hyponatremia
E8720CC 5387:17 codesAcidosis, unspecified
E8721CC 5388:17 codesAcute metabolic acidosis
E8722CC 5386:17 codesChronic metabolic acidosis
E8729CC 5397:17 codesOther acidosis
E873CC 5692:17 codesAlkalosis
E874CC 5693:17 codesMixed disorder of acid-base balance
E8802CC 6196:124 codesPlasminogen deficiency
E883MCC 6865:78 codesTumor lysis syndrome
E8840CC 6131:40 codesMitochondrial metabolism disorder, unspecified
E8841CC 6127:40 codesMELAS syndrome
E8842CC 6129:40 codesMERRF syndrome
E8843CC 6126:38 codesDisorders of mitochondrial tRNA synthetases
E8849CC 6137:41 codesOther mitochondrial metabolism disorders
E891CC 0520:434 codesPostprocedural hypoinsulinemia
E896CC 0526:23 codesPostprocedural adrenocortical (-medullary) hypofunction
E89810CC 0546:24 codesPostprocedural hemorrhage of an endocrine system organ or structure following an endocrine system procedure
E89811CC 0546:24 codesPostprocedural hemorrhage of an endocrine system organ or structure following other procedure
E89820CC 0546:24 codesPostprocedural hematoma of an endocrine system organ or structure following an endocrine system procedure
E89821CC 0546:24 codesPostprocedural hematoma of an endocrine system organ or structure following other procedure
E89822CC 0546:24 codesPostprocedural seroma of an endocrine system organ or structure following an endocrine system procedure
E89823CC 0546:24 codesPostprocedural seroma of an endocrine system organ or structure following other procedure
E8989CC 0546:24 codesOther postprocedural endocrine and metabolic complications and disorders
F01511CC 5408:40 codesVascular dementia, unspecified severity, with agitation
F01518CC 5419:40 codesVascular dementia, unspecified severity, with other behavioral disturbance
F0152CC 5648:40 codesVascular dementia, unspecified severity, with psychotic disturbance
F0153CC 5649:40 codesVascular dementia, unspecified severity, with mood disturbance
F0154CC 5651:40 codesVascular dementia, unspecified severity, with anxiety
F01A11CC 4966:40 codesVascular dementia, mild, with agitation
F01A18CC 5609:40 codesVascular dementia, mild, with other behavioral disturbance
F01A2CC 5428:40 codesVascular dementia, mild, with psychotic disturbance
F01A3CC 5430:40 codesVascular dementia, mild, with mood disturbance
F01A4CC 5431:40 codesVascular dementia, mild, with anxiety
F01B11CC 5519:40 codesVascular dementia, moderate, with agitation
F01B18CC 5557:40 codesVascular dementia, moderate, with other behavioral disturbance
F01B2CC 5414:40 codesVascular dementia, moderate, with psychotic disturbance
F01B3CC 5415:40 codesVascular dementia, moderate, with mood disturbance
F01B4CC 5416:40 codesVascular dementia, moderate, with anxiety
F01C11CC 4849:40 codesVascular dementia, severe, with agitation
F01C18CC 4932:40 codesVascular dementia, severe, with other behavioral disturbance
F01C2CC 5389:40 codesVascular dementia, severe, with psychotic disturbance
F01C3CC 5390:40 codesVascular dementia, severe, with mood disturbance
F01C4CC 5391:40 codesVascular dementia, severe, with anxiety
F02811CC 5406:40 codesDementia in other diseases classified elsewhere, unspecified severity, with agitation
F02818CC 5401:40 codesDementia in other diseases classified elsewhere, unspecified severity, with other behavioral disturbance
F0282CC 5042:40 codesDementia in other diseases classified elsewhere, unspecified severity, with psychotic disturbance
F0283CC 5041:40 codesDementia in other diseases classified elsewhere, unspecified severity, with mood disturbance
F0284CC 5044:40 codesDementia in other diseases classified elsewhere, unspecified severity, with anxiety
F02A11CC 5087:40 codesDementia in other diseases classified elsewhere, mild, with agitation
F02A18CC 5062:40 codesDementia in other diseases classified elsewhere, mild, with other behavioral disturbance
F02A2CC 4812:40 codesDementia in other diseases classified elsewhere, mild, with psychotic disturbance
F02A3CC 4814:40 codesDementia in other diseases classified elsewhere, mild, with mood disturbance
F02A4CC 4813:40 codesDementia in other diseases classified elsewhere, mild, with anxiety
F02B11CC 5614:40 codesDementia in other diseases classified elsewhere, moderate, with agitation
F02B18CC 5580:40 codesDementia in other diseases classified elsewhere, moderate, with other behavioral disturbance
F02B2CC 4793:40 codesDementia in other diseases classified elsewhere, moderate, with psychotic disturbance
F02B3CC 4791:40 codesDementia in other diseases classified elsewhere, moderate, with mood disturbance
F02B4CC 4796:40 codesDementia in other diseases classified elsewhere, moderate, with anxiety
F02C11CC 5559:40 codesDementia in other diseases classified elsewhere, severe, with agitation
F02C18CC 5551:40 codesDementia in other diseases classified elsewhere, severe, with other behavioral disturbance
F02C2CC 4768:40 codesDementia in other diseases classified elsewhere, severe, with psychotic disturbance
F02C3CC 4773:40 codesDementia in other diseases classified elsewhere, severe, with mood disturbance
F02C4CC 4770:40 codesDementia in other diseases classified elsewhere, severe, with anxiety
F03911CC 5384:40 codesUnspecified dementia, unspecified severity, with agitation
F03918CC 5381:40 codesUnspecified dementia, unspecified severity, with other behavioral disturbance
F0392CC 5646:40 codesUnspecified dementia, unspecified severity, with psychotic disturbance
F0393CC 5643:40 codesUnspecified dementia, unspecified severity, with mood disturbance



Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244
01 Mar 2023 06:12:40
CMS, code-revision=344, description-revision=1357