ICD-10-CM/PCS MS-DRG v42.0 Definitions Manual
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Part 1: List of CC and Major CC codes
Page 5 of 46
A000 A8182 C227 C8266 D57213 E8840 G1220 H47531 I63512 I8511 K55022 L97119 M3130 M84421A M86321 N00A O30213 O9883 Q76427 S0462XA S1234XK S22080B S3217XB S36128A S42241K S42464A S52033Q S52241N S52343K S52561Q S59149P S62308B S62646K S72041R S7221XK S72409Q S7291XC S82035P S82191B S82399C S82822P S89009K S92226P T2132XA T71193A T84194A
DxCC/MCCExclusionsDescription
D57213MCC 0545:49 codesSickle-cell/Hb-C disease with cerebral vascular involvement
D57214MCC 0545:49 codesSickle-cell/Hb-C disease with dactylitis
D57218MCC 0545:49 codesSickle-cell/Hb-C disease with crisis with other specified complication
D57219MCC 0544:125 codesSickle-cell/Hb-C disease with crisis, unspecified
D57411MCC 0544:125 codesSickle-cell thalassemia, unspecified, with acute chest syndrome
D57412MCC 0544:125 codesSickle-cell thalassemia, unspecified, with splenic sequestration
D57413MCC 0546:47 codesSickle-cell thalassemia, unspecified, with cerebral vascular involvement
D57414MCC 0546:47 codesSickle-cell thalassemia, unspecified, with dactylitis
D57418MCC 0546:47 codesSickle-cell thalassemia, unspecified, with crisis with other specified complication
D57419MCC 0544:125 codesSickle-cell thalassemia, unspecified, with crisis
D57431MCC 0547:51 codesSickle-cell thalassemia beta zero with acute chest syndrome
D57432MCC 0547:51 codesSickle-cell thalassemia beta zero with splenic sequestration
D57433MCC 0547:51 codesSickle-cell thalassemia beta zero with cerebral vascular involvement
D57434MCC 0547:51 codesSickle-cell thalassemia beta zero with dactylitis
D57438MCC 0547:51 codesSickle-cell thalassemia beta zero with crisis with other specified complication
D57439MCC 0547:51 codesSickle-cell thalassemia beta zero with crisis, unspecified
D57451MCC 0547:51 codesSickle-cell thalassemia beta plus with acute chest syndrome
D57452MCC 0547:51 codesSickle-cell thalassemia beta plus with splenic sequestration
D57453MCC 0547:51 codesSickle-cell thalassemia beta plus with cerebral vascular involvement
D57454MCC 0547:51 codesSickle-cell thalassemia beta plus with dactylitis
D57458MCC 0547:51 codesSickle-cell thalassemia beta plus with crisis with other specified complication
D57459MCC 0547:51 codesSickle-cell thalassemia beta plus with crisis, unspecified
D57811MCC 0544:125 codesOther sickle-cell disorders with acute chest syndrome
D57812MCC 0544:125 codesOther sickle-cell disorders with splenic sequestration
D57813MCC 0548:48 codesOther sickle-cell disorders with cerebral vascular involvement
D57814MCC 0548:48 codesOther sickle-cell disorders with dactylitis
D57818MCC 0548:48 codesOther sickle-cell disorders with crisis with other specified complication
D57819MCC 0544:125 codesOther sickle-cell disorders with crisis, unspecified
D588CC 0549:104 codesOther specified hereditary hemolytic anemias
D589CC 0549:104 codesHereditary hemolytic anemia, unspecified
D590CC 0550:112 codesDrug-induced autoimmune hemolytic anemia
D5910CC 0551:16 codesAutoimmune hemolytic anemia, unspecified
D5911CC 0551:16 codesWarm autoimmune hemolytic anemia
D5912CC 0551:16 codesCold autoimmune hemolytic anemia
D5913CC 0551:16 codesMixed type autoimmune hemolytic anemia
D5919CC 0551:16 codesOther autoimmune hemolytic anemia
D592CC 0550:112 codesDrug-induced nonautoimmune hemolytic anemia
D5930MCC 0552:110 codesHemolytic-uremic syndrome, unspecified
D5931MCC 0552:110 codesInfection-associated hemolytic-uremic syndrome
D5932MCC 0552:110 codesHereditary hemolytic-uremic syndrome
D5939MCC 0552:110 codesOther hemolytic-uremic syndrome
D594CC 0552:110 codesOther nonautoimmune hemolytic anemias
D599CC 0552:110 codesAcquired hemolytic anemia, unspecified
D600MCC 0552:110 codesChronic acquired pure red cell aplasia
D601MCC 0552:110 codesTransient acquired pure red cell aplasia
D608MCC 0552:110 codesOther acquired pure red cell aplasias
D609MCC 0552:110 codesAcquired pure red cell aplasia, unspecified
D6101CC 0553:98 codesConstitutional (pure) red blood cell aplasia
D6102CC 0554:101 codesShwachman-Diamond syndrome
D6103CC 0555:102 codesFanconi anemia
D6109CC 0555:102 codesOther constitutional aplastic anemia
D611MCC 0552:110 codesDrug-induced aplastic anemia
D612MCC 0552:110 codesAplastic anemia due to other external agents
D613MCC 0552:110 codesIdiopathic aplastic anemia
D61810MCC 0556:41 codesAntineoplastic chemotherapy induced pancytopenia
D61811MCC 0556:41 codesOther drug-induced pancytopenia
D61818CC 0556:41 codesOther pancytopenia
D6182CC 0556:41 codesMyelophthisis
D6189MCC 0552:110 codesOther specified aplastic anemias and other bone marrow failure syndromes
D619CC 0552:110 codesAplastic anemia, unspecified
D62CC 0557:111 codesAcute posthemorrhagic anemia
D65MCC 0558:50 codesDisseminated intravascular coagulation [defibrination syndrome]
D66MCC 0558:50 codesHereditary factor VIII deficiency
D67MCC 0558:50 codesHereditary factor IX deficiency
D6800CC 0559:49 codesVon Willebrand disease, unspecified
D6801CC 0559:49 codesVon Willebrand disease, type 1
D68020CC 0559:49 codesVon Willebrand disease, type 2A
D68021CC 0559:49 codesVon Willebrand disease, type 2B
D68022CC 0559:49 codesVon Willebrand disease, type 2M
D68023CC 0559:49 codesVon Willebrand disease, type 2N
D68029CC 0559:49 codesVon Willebrand disease, type 2, unspecified
D6803CC 0559:49 codesVon Willebrand disease, type 3
D6804CC 0559:49 codesAcquired von Willebrand disease
D6809CC 0559:49 codesOther von Willebrand disease
D681CC 0558:50 codesHereditary factor XI deficiency
D682CC 0558:50 codesHereditary deficiency of other clotting factors
D68311CC 0558:50 codesAcquired hemophilia
D68312CC 0560:50 codesAntiphospholipid antibody with hemorrhagic disorder
D68318CC 0558:50 codesOther hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors
D6832CC 0558:50 codesHemorrhagic disorder due to extrinsic circulating anticoagulants
D684CC 0558:50 codesAcquired coagulation factor deficiency
D6851CC 0561:38 codesActivated protein C resistance
D6852CC 0561:38 codesProthrombin gene mutation
D6859CC 0562:40 codesOther primary thrombophilia
D6861CC 0561:38 codesAntiphospholipid syndrome
D6862CC 0561:38 codesLupus anticoagulant syndrome
D6869CC 0562:40 codesOther thrombophilia
D688CC 0558:50 codesOther specified coagulation defects
D689CC 0558:50 codesCoagulation defect, unspecified
D690CC 0558:50 codesAllergic purpura
D693CC 0563:52 codesImmune thrombocytopenic purpura
D6941CC 0563:52 codesEvans syndrome
D6942CC 0563:52 codesCongenital and hereditary thrombocytopenia purpura
D740CC 0564:24 codesCongenital methemoglobinemia
D748CC 0564:24 codesOther methemoglobinemias
D749CC 0564:24 codesMethemoglobinemia, unspecified
D7581CC 0535:133 codesMyelofibrosis
D761CC 0565:39 codesHemophagocytic lymphohistiocytosis
D762CC 0566:39 codesHemophagocytic syndrome, infection-associated
D763CC 0567:39 codesOther histiocytosis syndromes
D7801CC 0568:78 codesIntraoperative hemorrhage and hematoma of the spleen complicating a procedure on the spleen
D7802CC 0568:78 codesIntraoperative hemorrhage and hematoma of the spleen complicating other procedure
D7811CC 0569:76 codesAccidental puncture and laceration of the spleen during a procedure on the spleen
D7812CC 0569:76 codesAccidental puncture and laceration of the spleen during other procedure
D7821CC 0568:78 codesPostprocedural hemorrhage of the spleen following a procedure on the spleen
D7822CC 0568:78 codesPostprocedural hemorrhage of the spleen following other procedure
D7831CC 0568:78 codesPostprocedural hematoma of the spleen following a procedure on the spleen
D7832CC 0568:78 codesPostprocedural hematoma of the spleen following other procedure
D7833CC 0568:78 codesPostprocedural seroma of the spleen following a procedure on the spleen
D7834CC 0568:78 codesPostprocedural seroma of the spleen following other procedure
D7881CC 0570:18 codesOther intraoperative complications of the spleen
D7889CC 0570:18 codesOther postprocedural complications of the spleen
D800CC 0571:44 codesHereditary hypogammaglobulinemia
D801CC 0572:46 codesNonfamilial hypogammaglobulinemia
D802CC 0572:46 codesSelective deficiency of immunoglobulin A [IgA]
D803CC 0571:44 codesSelective deficiency of immunoglobulin G [IgG] subclasses
D804CC 0571:44 codesSelective deficiency of immunoglobulin M [IgM]
D805CC 0571:44 codesImmunodeficiency with increased immunoglobulin M [IgM]
D806CC 0571:44 codesAntibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
D807CC 0571:44 codesTransient hypogammaglobulinemia of infancy
D808CC 0571:44 codesOther immunodeficiencies with predominantly antibody defects
D809CC 0571:44 codesImmunodeficiency with predominantly antibody defects, unspecified
D810CC 0571:44 codesSevere combined immunodeficiency [SCID] with reticular dysgenesis
D811CC 0571:44 codesSevere combined immunodeficiency [SCID] with low T- and B-cell numbers
D812CC 0571:44 codesSevere combined immunodeficiency [SCID] with low or normal B-cell numbers
D8130CC 0573:35 codesAdenosine deaminase deficiency, unspecified
D8131CC 0573:35 codesSevere combined immunodeficiency due to adenosine deaminase deficiency
D8132CC 0573:35 codesAdenosine deaminase 2 deficiency
D8139CC 0573:35 codesOther adenosine deaminase deficiency
D814CC 0571:44 codesNezelof's syndrome
D815CC 0573:35 codesPurine nucleoside phosphorylase [PNP] deficiency
D816CC 0571:44 codesMajor histocompatibility complex class I deficiency
D817CC 0571:44 codesMajor histocompatibility complex class II deficiency
D8182CC 0571:44 codesActivated Phosphoinositide 3-kinase Delta Syndrome [APDS]
D8189CC 0571:44 codesOther combined immunodeficiencies
D819CC 0571:44 codesCombined immunodeficiency, unspecified
D820CC 0571:44 codesWiskott-Aldrich syndrome
D821CC 0571:44 codesDi George's syndrome
D830CC 0571:44 codesCommon variable immunodeficiency with predominant abnormalities of B-cell numbers and function
D831CC 0571:44 codesCommon variable immunodeficiency with predominant immunoregulatory T-cell disorders
D832CC 0571:44 codesCommon variable immunodeficiency with autoantibodies to B- or T-cells
D838CC 0571:44 codesOther common variable immunodeficiencies
D839CC 0571:44 codesCommon variable immunodeficiency, unspecified
D8481CC 0571:44 codesImmunodeficiency due to conditions classified elsewhere
D84821CC 0571:44 codesImmunodeficiency due to drugs
D84822CC 0571:44 codesImmunodeficiency due to external causes
D8489CC 0571:44 codesOther immunodeficiencies
D849CC 0571:44 codesImmunodeficiency, unspecified
D89810CC 0574:45 codesAcute graft-versus-host disease
D89811CC 0574:45 codesChronic graft-versus-host disease
D89812CC 0574:45 codesAcute on chronic graft-versus-host disease
D89813CC 0574:45 codesGraft-versus-host disease, unspecified
D89833CC No ExclCytokine release syndrome, grade 3
D89834CC No ExclCytokine release syndrome, grade 4
D89835CC No ExclCytokine release syndrome, grade 5
E035MCC 0575:717 codesMyxedema coma
E0501MCC 0576:59 codesThyrotoxicosis with diffuse goiter with thyrotoxic crisis or storm
E0511MCC 0576:59 codesThyrotoxicosis with toxic single thyroid nodule with thyrotoxic crisis or storm
E0521MCC 0576:59 codesThyrotoxicosis with toxic multinodular goiter with thyrotoxic crisis or storm
E0531MCC 0576:59 codesThyrotoxicosis from ectopic thyroid tissue with thyrotoxic crisis or storm
E0541MCC 0576:59 codesThyrotoxicosis factitia with thyrotoxic crisis or storm
E0581MCC 0576:59 codesOther thyrotoxicosis with thyrotoxic crisis or storm
E0591MCC 0576:59 codesThyrotoxicosis, unspecified with thyrotoxic crisis or storm
E060CC 0577:7 codesAcute thyroiditis
E0800MCC 0578:351 codesDiabetes mellitus due to underlying condition with hyperosmolarity without nonketotic hyperglycemic-hyperosmolar coma (NKHHC)
E0801MCC 0578:351 codesDiabetes mellitus due to underlying condition with hyperosmolarity with coma
E0810MCC 0578:351 codesDiabetes mellitus due to underlying condition with ketoacidosis without coma
E0811MCC 0578:351 codesDiabetes mellitus due to underlying condition with ketoacidosis with coma
E0852CC 0579:45 codesDiabetes mellitus due to underlying condition with diabetic peripheral angiopathy with gangrene
E08641MCC 0578:351 codesDiabetes mellitus due to underlying condition with hypoglycemia with coma
E0900MCC 0578:351 codesDrug or chemical induced diabetes mellitus with hyperosmolarity without nonketotic hyperglycemic-hyperosmolar coma (NKHHC)
E0901MCC 0578:351 codesDrug or chemical induced diabetes mellitus with hyperosmolarity with coma
E0910MCC 0578:351 codesDrug or chemical induced diabetes mellitus with ketoacidosis without coma
E0911MCC 0578:351 codesDrug or chemical induced diabetes mellitus with ketoacidosis with coma
E0952CC 0580:46 codesDrug or chemical induced diabetes mellitus with diabetic peripheral angiopathy with gangrene
E09641MCC 0578:351 codesDrug or chemical induced diabetes mellitus with hypoglycemia with coma
E1010MCC 0581:354 codesType 1 diabetes mellitus with ketoacidosis without coma
E1011MCC 0581:354 codesType 1 diabetes mellitus with ketoacidosis with coma
E1052CC 0582:46 codesType 1 diabetes mellitus with diabetic peripheral angiopathy with gangrene
E10641MCC 0581:354 codesType 1 diabetes mellitus with hypoglycemia with coma
E1100MCC 0578:351 codesType 2 diabetes mellitus with hyperosmolarity without nonketotic hyperglycemic-hyperosmolar coma (NKHHC)
E1101MCC 0578:351 codesType 2 diabetes mellitus with hyperosmolarity with coma
E1110MCC 0578:351 codesType 2 diabetes mellitus with ketoacidosis without coma
E1111MCC 0578:351 codesType 2 diabetes mellitus with ketoacidosis with coma
E1152CC 0583:46 codesType 2 diabetes mellitus with diabetic peripheral angiopathy with gangrene
E11641MCC 0578:351 codesType 2 diabetes mellitus with hypoglycemia with coma
E1300MCC 0578:351 codesOther specified diabetes mellitus with hyperosmolarity without nonketotic hyperglycemic-hyperosmolar coma (NKHHC)
E1301MCC 0578:351 codesOther specified diabetes mellitus with hyperosmolarity with coma
E1310MCC 0578:351 codesOther specified diabetes mellitus with ketoacidosis without coma
E1311MCC 0578:351 codesOther specified diabetes mellitus with ketoacidosis with coma
E1352CC 0584:46 codesOther specified diabetes mellitus with diabetic peripheral angiopathy with gangrene
E13641MCC 0578:351 codesOther specified diabetes mellitus with hypoglycemia with coma
E15CC 0581:354 codesNondiabetic hypoglycemic coma
E221CC 0585:4 codesHyperprolactinemia
E222CC 0586:18 codesSyndrome of inappropriate secretion of antidiuretic hormone
E228CC 0585:4 codesOther hyperfunction of pituitary gland
E229CC 0585:4 codesHyperfunction of pituitary gland, unspecified
E230CC 0587:21 codesHypopituitarism
E232CC 0588:19 codesDiabetes insipidus
E240CC 0589:23 codesPituitary-dependent Cushing's disease
E242CC 0589:23 codesDrug-induced Cushing's syndrome
E243CC 0589:23 codesEctopic ACTH syndrome
E244CC 0589:23 codesAlcohol-induced pseudo-Cushing's syndrome
E248CC 0589:23 codesOther Cushing's syndrome
E249CC 0589:23 codesCushing's syndrome, unspecified
E270CC 0590:22 codesOther adrenocortical overactivity
E271CC 0590:22 codesPrimary adrenocortical insufficiency
E272CC 0590:22 codesAddisonian crisis
E273CC 0590:22 codesDrug-induced adrenocortical insufficiency
E2740CC 0590:22 codesUnspecified adrenocortical insufficiency
E2749CC 0590:22 codesOther adrenocortical insufficiency
E275CC 0590:22 codesAdrenomedullary hyperfunction
E321CC 0591:11 codesAbscess of thymus
E3400CC 0592:11 codesCarcinoid syndrome, unspecified
E3401CC 0592:11 codesCarcinoid heart syndrome
E3409CC 0592:11 codesOther carcinoid syndrome
E3601CC 0593:78 codesIntraoperative hemorrhage and hematoma of an endocrine system organ or structure complicating an endocrine system procedure
E3602CC 0593:78 codesIntraoperative hemorrhage and hematoma of an endocrine system organ or structure complicating other procedure
E3611CC 0569:76 codesAccidental puncture and laceration of an endocrine system organ or structure during an endocrine system procedure
E3612CC 0569:76 codesAccidental puncture and laceration of an endocrine system organ or structure during other procedure
E40MCC 0594:9 codesKwashiorkor
E41MCC 0594:9 codesNutritional marasmus
E42MCC 0594:9 codesMarasmic kwashiorkor
E43MCC 0594:9 codesUnspecified severe protein-calorie malnutrition
E440CC 0594:9 codesModerate protein-calorie malnutrition
E441CC 0594:9 codesMild protein-calorie malnutrition
E45CC 0594:9 codesRetarded development following protein-calorie malnutrition
E46CC 0594:9 codesUnspecified protein-calorie malnutrition
E5111CC 0595:34 codesDry beriberi
E5112CC 0595:34 codesWet beriberi
E512CC 0595:34 codesWernicke's encephalopathy
E518CC 0595:34 codesOther manifestations of thiamine deficiency
E519CC 0595:34 codesThiamine deficiency, unspecified
E530CC 0595:34 codesRiboflavin deficiency
E550CC 0596:34 codesRickets, active
E640CC 0594:9 codesSequelae of protein-calorie malnutrition
E662CC 0597:13 codesMorbid (severe) obesity with alveolar hypoventilation
E700CC 0598:131 codesClassical phenylketonuria
E701CC 0598:131 codesOther hyperphenylalaninemias
E7020CC 0598:131 codesDisorder of tyrosine metabolism, unspecified
E7021CC 0598:131 codesTyrosinemia
E7029CC 0598:131 codesOther disorders of tyrosine metabolism
E7030CC 0598:131 codesAlbinism, unspecified
E70310CC 0598:131 codesX-linked ocular albinism
E70311CC 0598:131 codesAutosomal recessive ocular albinism
E70318CC 0598:131 codesOther ocular albinism
E70319CC 0598:131 codesOcular albinism, unspecified
E70320CC 0598:131 codesTyrosinase negative oculocutaneous albinism
E70321CC 0598:131 codesTyrosinase positive oculocutaneous albinism
E70328CC 0598:131 codesOther oculocutaneous albinism
E70329CC 0598:131 codesOculocutaneous albinism, unspecified
E70330CC 0598:131 codesChediak-Higashi syndrome
E70331CC 0598:131 codesHermansky-Pudlak syndrome
E70338CC 0598:131 codesOther albinism with hematologic abnormality
E70339CC 0598:131 codesAlbinism with hematologic abnormality, unspecified
E7039CC 0598:131 codesOther specified albinism
E7040CC 0598:131 codesDisorders of histidine metabolism, unspecified
E7041CC 0598:131 codesHistidinemia
E7049CC 0598:131 codesOther disorders of histidine metabolism
E705CC 0598:131 codesDisorders of tryptophan metabolism
E7081CC 0599:8 codesAromatic L-amino acid decarboxylase deficiency
E7089CC 0599:8 codesOther disorders of aromatic amino-acid metabolism
E709CC 0598:131 codesDisorder of aromatic amino-acid metabolism, unspecified
E710CC 0598:131 codesMaple-syrup-urine disease
E71110CC 0598:131 codesIsovaleric acidemia
E71111CC 0598:131 codes3-methylglutaconic aciduria
E71118CC 0598:131 codesOther branched-chain organic acidurias
E71120CC 0598:131 codesMethylmalonic acidemia
E71121CC 0598:131 codesPropionic acidemia
E71128CC 0598:131 codesOther disorders of propionate metabolism
E7119CC 0598:131 codesOther disorders of branched-chain amino-acid metabolism
E712CC 0598:131 codesDisorder of branched-chain amino-acid metabolism, unspecified
E71310CC 0600:39 codesLong chain/very long chain acyl CoA dehydrogenase deficiency
E71311CC 0601:39 codesMedium chain acyl CoA dehydrogenase deficiency
E71312CC 0602:39 codesShort chain acyl CoA dehydrogenase deficiency
E71313CC 0603:39 codesGlutaric aciduria type II
E71314CC 0604:39 codesMuscle carnitine palmitoyltransferase deficiency
E71318CC 0605:39 codesOther disorders of fatty-acid oxidation
E7132CC 0606:39 codesDisorders of ketone metabolism
E7139CC 0607:41 codesOther disorders of fatty-acid metabolism
E7150CC 0608:36 codesPeroxisomal disorder, unspecified
E71510CC 0609:36 codesZellweger syndrome
E71511CC 0610:36 codesNeonatal adrenoleukodystrophy
E71518CC 0611:36 codesOther disorders of peroxisome biogenesis
E71520CC 0612:36 codesChildhood cerebral X-linked adrenoleukodystrophy
E71521CC 0613:36 codesAdolescent X-linked adrenoleukodystrophy
E71522CC 0614:36 codesAdrenomyeloneuropathy
E71528CC 0615:36 codesOther X-linked adrenoleukodystrophy
E71529CC 0616:36 codesX-linked adrenoleukodystrophy, unspecified type
E7153CC 0617:36 codesOther group 2 peroxisomal disorders
E71540CC 0618:36 codesRhizomelic chondrodysplasia punctata
E71541CC 0619:36 codesZellweger-like syndrome
E71542CC 0620:36 codesOther group 3 peroxisomal disorders
E71548CC 0621:36 codesOther peroxisomal disorders
E7200CC 0598:131 codesDisorders of amino-acid transport, unspecified
E7201CC 0598:131 codesCystinuria
E7202CC 0598:131 codesHartnup's disease
E7203CC 0622:1 codeLowe's syndrome
E7204CC 0598:131 codesCystinosis
E7209CC 0598:131 codesOther disorders of amino-acid transport
E7210CC 0598:131 codesDisorders of sulfur-bearing amino-acid metabolism, unspecified
E7211CC 0598:131 codesHomocystinuria
E7212CC 0598:131 codesMethylenetetrahydrofolate reductase deficiency
E7219CC 0598:131 codesOther disorders of sulfur-bearing amino-acid metabolism
E7220CC 0598:131 codesDisorder of urea cycle metabolism, unspecified
E7221CC 0598:131 codesArgininemia
E7222CC 0598:131 codesArginosuccinic aciduria
E7223CC 0598:131 codesCitrullinemia
E7229CC 0598:131 codesOther disorders of urea cycle metabolism
E723CC 0598:131 codesDisorders of lysine and hydroxylysine metabolism
E724CC 0598:131 codesDisorders of ornithine metabolism
E7250CC 0598:131 codesDisorder of glycine metabolism, unspecified
E7251CC 0598:131 codesNon-ketotic hyperglycinemia
E7252CC 0598:131 codesTrimethylaminuria
E7253CC 0598:131 codesPrimary hyperoxaluria
E7259CC 0598:131 codesOther disorders of glycine metabolism
E7281CC 0598:131 codesDisorders of gamma aminobutyric acid metabolism
E7289CC 0598:131 codesOther specified disorders of amino-acid metabolism
E729CC 0598:131 codesDisorder of amino-acid metabolism, unspecified
E7400CC 0598:131 codesGlycogen storage disease, unspecified
E7401CC 0598:131 codesvon Gierke disease
E7402CC 0598:131 codesPompe disease
E7403CC 0598:131 codesCori disease
E7404CC 0598:131 codesMcArdle disease
E7405CC 0623:128 codesLysosome-associated membrane protein 2 [LAMP2] deficiency
E7409CC 0598:131 codesOther glycogen storage disease
E7420CC 0598:131 codesDisorders of galactose metabolism, unspecified
E7421CC 0598:131 codesGalactosemia
E7429CC 0598:131 codesOther disorders of galactose metabolism
E744CC 0598:131 codesDisorders of pyruvate metabolism and gluconeogenesis
E74810CC 0624:53 codesGlucose transporter protein type 1 deficiency
E74818CC 0624:53 codesOther disorders of glucose transport
E74819CC 0624:53 codesDisorders of glucose transport, unspecified
E74820CC 0624:53 codesSLC13A5 Citrate Transporter Disorder
E74829CC 0624:53 codesOther disorders of citrate metabolism
E7489CC 0624:53 codesOther specified disorders of carbohydrate metabolism
E7500CC 0625:25 codesGM2 gangliosidosis, unspecified
E7501CC 0625:25 codesSandhoff disease
E7502CC 0625:25 codesTay-Sachs disease
E7509CC 0625:25 codesOther GM2 gangliosidosis
E7510CC 0625:25 codesUnspecified gangliosidosis
E7511CC 0625:25 codesMucolipidosis IV
E7519CC 0625:25 codesOther gangliosidosis
E7523CC 0626:24 codesKrabbe disease
E7525CC 0626:24 codesMetachromatic leukodystrophy
E7526CC 0626:24 codesSulfatase deficiency
E7527CC 0626:24 codesPelizaeus-Merzbacher disease
E7528CC 0626:24 codesCanavan disease
E7529CC 0626:24 codesOther sphingolipidosis
E754CC 0625:25 codesNeuronal ceroid lipofuscinosis
E7601CC 0627:37 codesHurler's syndrome
E7602CC 0627:37 codesHurler-Scheie syndrome
E7603CC 0627:37 codesScheie's syndrome
E761CC 0627:37 codesMucopolysaccharidosis, type II
E76210CC 0627:37 codesMorquio A mucopolysaccharidoses
E76211CC 0627:37 codesMorquio B mucopolysaccharidoses
E76219CC 0627:37 codesMorquio mucopolysaccharidoses, unspecified
E7622CC 0627:37 codesSanfilippo mucopolysaccharidoses
E7629CC 0627:37 codesOther mucopolysaccharidoses
E763CC 0627:37 codesMucopolysaccharidosis, unspecified
E768CC 0627:37 codesOther disorders of glucosaminoglycan metabolism
E769CC 0627:37 codesGlucosaminoglycan metabolism disorder, unspecified
E7871CC 0628:21 codesBarth syndrome
E7872CC 0628:21 codesSmith-Lemli-Opitz syndrome
E791CC 0573:35 codesLesch-Nyhan syndrome
E792CC 0573:35 codesMyoadenylate deaminase deficiency
E7981CC 0573:35 codesAicardi-Goutieres syndrome
E7982CC 0573:35 codesHereditary xanthinuria
E7989CC 0573:35 codesOther specified disorders of purine and pyrimidine metabolism
E799CC 0573:35 codesDisorder of purine and pyrimidine metabolism, unspecified
E800CC 0573:35 codesHereditary erythropoietic porphyria
E801CC 0573:35 codesPorphyria cutanea tarda
E8020CC 0573:35 codesUnspecified porphyria
E8021CC 0573:35 codesAcute intermittent (hepatic) porphyria
E8029CC 0573:35 codesOther porphyria
E803CC 0629:41 codesDefects of catalase and peroxidase
E840MCC 0630:5 codesCystic fibrosis with pulmonary manifestations
E8411MCC 0630:5 codesMeconium ileus in cystic fibrosis
E8419CC 0630:5 codesCystic fibrosis with other intestinal manifestations
E848CC 0630:5 codesCystic fibrosis with other manifestations
E849CC 0630:5 codesCystic fibrosis, unspecified
E850CC 0631:10 codesNon-neuropathic heredofamilial amyloidosis
E851CC 0631:10 codesNeuropathic heredofamilial amyloidosis
E852CC 0631:10 codesHeredofamilial amyloidosis, unspecified
E853CC 0631:10 codesSecondary systemic amyloidosis
E854CC 0631:10 codesOrgan-limited amyloidosis
E8581CC 0631:10 codesLight chain (AL) amyloidosis
E8582CC 0631:10 codesWild-type transthyretin-related (ATTR) amyloidosis
E8589CC 0631:10 codesOther amyloidosis
E859CC 0631:10 codesAmyloidosis, unspecified
E870CC 0632:17 codesHyperosmolality and hypernatremia
E871CC 0632:17 codesHypo-osmolality and hyponatremia
E8720CC 0632:17 codesAcidosis, unspecified
E8721CC 0632:17 codesAcute metabolic acidosis
E8722CC 0632:17 codesChronic metabolic acidosis
E8729CC 0632:17 codesOther acidosis
E873CC 0632:17 codesAlkalosis
E874CC 0632:17 codesMixed disorder of acid-base balance
E8802CC 0633:127 codesPlasminogen deficiency
E883MCC 0634:73 codesTumor lysis syndrome



Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244
29 Mar 2024 17:03:46
CMS, code-revision=361, description-revision=1397