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 1210 of 1324
PDX Collection 6616 (continued)
Q2549Other congenital malformations of aorta
Q258Other congenital malformations of other great arteries
Q259Congenital malformation of great arteries, unspecified
Q2730Arteriovenous malformation, site unspecified
Q274Congenital phlebectasia
Q280Arteriovenous malformation of precerebral vessels
Q281Other malformations of precerebral vessels
Q288Other specified congenital malformations of circulatory system
Q289Congenital malformation of circulatory system, unspecified
Q872Congenital malformation syndromes predominantly involving limbs
Q873Congenital malformation syndromes involving early overgrowth
Q875Other congenital malformation syndromes with other skeletal changes
Q8781Alport syndrome
Q8782Arterial tortuosity syndrome
Q8783Bardet-Biedl syndrome
Q8784Laurence-Moon syndrome
Q8785MED13L syndrome
Q8789Other specified congenital malformation syndromes, not elsewhere classified
Q897Multiple congenital malformations, not elsewhere classified
Q898Other specified congenital malformations
 
PDX Collection 6617
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
Q251Coarctation of aorta
Q2521Interruption of aortic arch
Q2529Other atresia of aorta
Q253Supravalvular aortic stenosis
Q2540Congenital malformation of aorta unspecified
Q2541Absence and aplasia of aorta
Q2542Hypoplasia of aorta
Q2543Congenital aneurysm of aorta
Q2544Congenital dilation of aorta
Q2545Double aortic arch
Q2546Tortuous aortic arch
Q2547Right aortic arch
Q2548Anomalous origin of subclavian artery
Q2549Other congenital malformations of aorta
Q258Other congenital malformations of other great arteries
Q259Congenital malformation of great arteries, unspecified
Q2730Arteriovenous malformation, site unspecified
Q274Congenital phlebectasia
Q280Arteriovenous malformation of precerebral vessels
Q281Other malformations of precerebral vessels
Q288Other specified congenital malformations of circulatory system
Q289Congenital malformation of circulatory system, unspecified
Q872Congenital malformation syndromes predominantly involving limbs
Q873Congenital malformation syndromes involving early overgrowth
Q875Other congenital malformation syndromes with other skeletal changes
Q8781Alport syndrome
Q8782Arterial tortuosity syndrome
Q8783Bardet-Biedl syndrome
Q8784Laurence-Moon syndrome
Q8785MED13L syndrome
Q8789Other specified congenital malformation syndromes, not elsewhere classified
Q897Multiple congenital malformations, not elsewhere classified
Q898Other specified congenital malformations
 
PDX Collection 6618
K3189Other diseases of stomach and duodenum
K319Disease of stomach and duodenum, unspecified
K35200Acute appendicitis with generalized peritonitis, without perforation or abscess
K35201Acute appendicitis with generalized peritonitis, with perforation, without abscess
K35209Acute appendicitis with generalized peritonitis, without abscess, unspecified as to perforation
K35210Acute appendicitis with generalized peritonitis, without perforation, with abscess
K35211Acute appendicitis with generalized peritonitis, with perforation and abscess
K35219Acute appendicitis with generalized peritonitis, with abscess, unspecified as to perforation
K3530Acute appendicitis with localized peritonitis, without perforation or gangrene
K3531Acute appendicitis with localized peritonitis and gangrene, without perforation
K3532Acute appendicitis with perforation, localized peritonitis, and gangrene, without abscess
K3533Acute appendicitis with perforation, localized peritonitis, and gangrene, with abscess
K3580Unspecified acute appendicitis
K35890Other acute appendicitis without perforation or gangrene
K35891Other acute appendicitis without perforation, with gangrene
K36Other appendicitis
K37Unspecified appendicitis
K380Hyperplasia of appendix
K381Appendicular concretions
K382Diverticulum of appendix
K383Fistula of appendix
K388Other specified diseases of appendix
K389Disease of appendix, unspecified
K9281Gastrointestinal mucositis (ulcerative)
 
PDX Collection 6619
C880Waldenstrom macroglobulinemia
D472Monoclonal gammopathy
D890Polyclonal hypergammaglobulinemia
D891Cryoglobulinemia
E700Classical phenylketonuria
E701Other hyperphenylalaninemias
E7020Disorder of tyrosine metabolism, unspecified
E7021Tyrosinemia
E7029Other disorders of tyrosine metabolism
E7030Albinism, unspecified
E70310X-linked ocular albinism
E70311Autosomal recessive ocular albinism
E70318Other ocular albinism
E70319Ocular albinism, unspecified
E70320Tyrosinase negative oculocutaneous albinism
E70321Tyrosinase positive oculocutaneous albinism
E70328Other oculocutaneous albinism
E70329Oculocutaneous albinism, unspecified
E70330Chediak-Higashi syndrome
E70331Hermansky-Pudlak syndrome
E70338Other albinism with hematologic abnormality
E70339Albinism with hematologic abnormality, unspecified
E7039Other specified albinism
E7040Disorders of histidine metabolism, unspecified
E7041Histidinemia
E7049Other disorders of histidine metabolism
E705Disorders of tryptophan metabolism
E7081Aromatic L-amino acid decarboxylase deficiency
E7089Other disorders of aromatic amino-acid metabolism
E709Disorder of aromatic amino-acid metabolism, unspecified
E710Maple-syrup-urine disease
E71110Isovaleric acidemia
E711113-methylglutaconic aciduria
E71118Other branched-chain organic acidurias
E71120Methylmalonic acidemia
E71121Propionic acidemia
E71128Other disorders of propionate metabolism
E7119Other disorders of branched-chain amino-acid metabolism
E712Disorder of branched-chain amino-acid metabolism, unspecified
E7130Disorder of fatty-acid metabolism, unspecified
E7200Disorders of amino-acid transport, unspecified
E7201Cystinuria
E7202Hartnup's disease
E7204Cystinosis
E7209Other disorders of amino-acid transport
E7210Disorders of sulfur-bearing amino-acid metabolism, unspecified
E7211Homocystinuria
E7212Methylenetetrahydrofolate reductase deficiency
E7219Other disorders of sulfur-bearing amino-acid metabolism
E7220Disorder of urea cycle metabolism, unspecified
E7221Argininemia
E7222Arginosuccinic aciduria
E7223Citrullinemia
E7229Other disorders of urea cycle metabolism
E723Disorders of lysine and hydroxylysine metabolism
E724Disorders of ornithine metabolism
E7250Disorder of glycine metabolism, unspecified
E7251Non-ketotic hyperglycinemia
E7252Trimethylaminuria
E7253Primary hyperoxaluria
E7259Other disorders of glycine metabolism
E7281Disorders of gamma aminobutyric acid metabolism
E7289Other specified disorders of amino-acid metabolism
E729Disorder of amino-acid metabolism, unspecified
E730Congenital lactase deficiency
E731Secondary lactase deficiency
E738Other lactose intolerance
E739Lactose intolerance, unspecified
E7400Glycogen storage disease, unspecified
E7401von Gierke disease
E7402Pompe disease
E7403Cori disease
E7404McArdle disease
E7405Lysosome-associated membrane protein 2 [LAMP2] deficiency
E7409Other glycogen storage disease
E7410Disorder of fructose metabolism, unspecified
E7411Essential fructosuria
E7412Hereditary fructose intolerance
E7419Other disorders of fructose metabolism
E7420Disorders of galactose metabolism, unspecified
E7421Galactosemia
E7429Other disorders of galactose metabolism
E7431Sucrase-isomaltase deficiency
E7439Other disorders of intestinal carbohydrate absorption
E744Disorders of pyruvate metabolism and gluconeogenesis
E74810Glucose transporter protein type 1 deficiency
E74818Other disorders of glucose transport
E74819Disorders of glucose transport, unspecified
E7489Other specified disorders of carbohydrate metabolism
E749Disorder of carbohydrate metabolism, unspecified
E7521Fabry (-Anderson) disease
E7522Gaucher disease
E75240Niemann-Pick disease type A
E75241Niemann-Pick disease type B
E75242Niemann-Pick disease type C
E75243Niemann-Pick disease type D
E75248Other Niemann-Pick disease
E75249Niemann-Pick disease, unspecified
E753Sphingolipidosis, unspecified
E755Other lipid storage disorders
E756Lipid storage disorder, unspecified
E770Defects in post-translational modification of lysosomal enzymes
E771Defects in glycoprotein degradation
E778Other disorders of glycoprotein metabolism
E779Disorder of glycoprotein metabolism, unspecified
E7800Pure hypercholesterolemia, unspecified
E7801Familial hypercholesterolemia
E781Pure hyperglyceridemia
E782Mixed hyperlipidemia
E783Hyperchylomicronemia
E7841Elevated Lipoprotein(a)
E7849Other hyperlipidemia
E785Hyperlipidemia, unspecified
E786Lipoprotein deficiency
E7870Disorder of bile acid and cholesterol metabolism, unspecified
E7879Other disorders of bile acid and cholesterol metabolism
E7881Lipoid dermatoarthritis
E7889Other lipoprotein metabolism disorders
E789Disorder of lipoprotein metabolism, unspecified
E8802Plasminogen deficiency
E8809Other disorders of plasma-protein metabolism, not elsewhere classified
E881Lipodystrophy, not elsewhere classified
E882Lipomatosis, not elsewhere classified
E88811Insulin resistance syndrome, Type A
E88818Other insulin resistance
E88819Insulin resistance, unspecified
E8889Other specified metabolic disorders
 
PDX Collection 6620
C880Waldenstrom macroglobulinemia
D472Monoclonal gammopathy
D890Polyclonal hypergammaglobulinemia
D891Cryoglobulinemia
E700Classical phenylketonuria
E701Other hyperphenylalaninemias
E7020Disorder of tyrosine metabolism, unspecified
E7021Tyrosinemia
E7029Other disorders of tyrosine metabolism
E7030Albinism, unspecified
E70310X-linked ocular albinism
E70311Autosomal recessive ocular albinism
E70318Other ocular albinism
E70319Ocular albinism, unspecified
E70320Tyrosinase negative oculocutaneous albinism
E70321Tyrosinase positive oculocutaneous albinism
E70328Other oculocutaneous albinism
E70329Oculocutaneous albinism, unspecified
E70330Chediak-Higashi syndrome
E70331Hermansky-Pudlak syndrome
E70338Other albinism with hematologic abnormality
E70339Albinism with hematologic abnormality, unspecified
E7039Other specified albinism
E7040Disorders of histidine metabolism, unspecified
E7041Histidinemia
E7049Other disorders of histidine metabolism
E705Disorders of tryptophan metabolism
E7081Aromatic L-amino acid decarboxylase deficiency
E7089Other disorders of aromatic amino-acid metabolism
E709Disorder of aromatic amino-acid metabolism, unspecified
E710Maple-syrup-urine disease
E71110Isovaleric acidemia
E711113-methylglutaconic aciduria
E71118Other branched-chain organic acidurias
E71120Methylmalonic acidemia
E71121Propionic acidemia
E71128Other disorders of propionate metabolism
E7119Other disorders of branched-chain amino-acid metabolism
E712Disorder of branched-chain amino-acid metabolism, unspecified
E7130Disorder of fatty-acid metabolism, unspecified
E7200Disorders of amino-acid transport, unspecified
E7201Cystinuria
E7202Hartnup's disease
E7204Cystinosis
E7209Other disorders of amino-acid transport
E7210Disorders of sulfur-bearing amino-acid metabolism, unspecified
E7211Homocystinuria
E7212Methylenetetrahydrofolate reductase deficiency
E7219Other disorders of sulfur-bearing amino-acid metabolism
E7220Disorder of urea cycle metabolism, unspecified
E7221Argininemia
E7222Arginosuccinic aciduria
E7223Citrullinemia
E7229Other disorders of urea cycle metabolism
E723Disorders of lysine and hydroxylysine metabolism
E724Disorders of ornithine metabolism
E7250Disorder of glycine metabolism, unspecified
E7251Non-ketotic hyperglycinemia
E7252Trimethylaminuria
E7253Primary hyperoxaluria
E7259Other disorders of glycine metabolism
E7281Disorders of gamma aminobutyric acid metabolism
E7289Other specified disorders of amino-acid metabolism
E729Disorder of amino-acid metabolism, unspecified
E730Congenital lactase deficiency
E731Secondary lactase deficiency
E738Other lactose intolerance
E739Lactose intolerance, unspecified
E7400Glycogen storage disease, unspecified
E7401von Gierke disease
E7402Pompe disease
E7403Cori disease
E7404McArdle disease
E7405Lysosome-associated membrane protein 2 [LAMP2] deficiency
E7409Other glycogen storage disease
E7410Disorder of fructose metabolism, unspecified
E7411Essential fructosuria
E7412Hereditary fructose intolerance
E7419Other disorders of fructose metabolism
E7420Disorders of galactose metabolism, unspecified
E7421Galactosemia
E7429Other disorders of galactose metabolism
E7431Sucrase-isomaltase deficiency
E7439Other disorders of intestinal carbohydrate absorption
E744Disorders of pyruvate metabolism and gluconeogenesis
E74810Glucose transporter protein type 1 deficiency
E74818Other disorders of glucose transport
E74819Disorders of glucose transport, unspecified
E7489Other specified disorders of carbohydrate metabolism
E749Disorder of carbohydrate metabolism, unspecified
E7521Fabry (-Anderson) disease
E7522Gaucher disease
E75240Niemann-Pick disease type A
E75241Niemann-Pick disease type B
E75242Niemann-Pick disease type C
E75243Niemann-Pick disease type D
E75248Other Niemann-Pick disease
E75249Niemann-Pick disease, unspecified
E753Sphingolipidosis, unspecified
E755Other lipid storage disorders
E756Lipid storage disorder, unspecified
E770Defects in post-translational modification of lysosomal enzymes
E771Defects in glycoprotein degradation
E778Other disorders of glycoprotein metabolism
E779Disorder of glycoprotein metabolism, unspecified
E7800Pure hypercholesterolemia, unspecified
E7801Familial hypercholesterolemia
E781Pure hyperglyceridemia
E782Mixed hyperlipidemia
E783Hyperchylomicronemia
E7841Elevated Lipoprotein(a)
E7849Other hyperlipidemia
E785Hyperlipidemia, unspecified
E786Lipoprotein deficiency
E7870Disorder of bile acid and cholesterol metabolism, unspecified
E7879Other disorders of bile acid and cholesterol metabolism
E7881Lipoid dermatoarthritis
E7889Other lipoprotein metabolism disorders
E789Disorder of lipoprotein metabolism, unspecified
E8802Plasminogen deficiency
E8809Other disorders of plasma-protein metabolism, not elsewhere classified
E881Lipodystrophy, not elsewhere classified
E882Lipomatosis, not elsewhere classified
E88811Insulin resistance syndrome, Type A
E88818Other insulin resistance
E88819Insulin resistance, unspecified
E8889Other specified metabolic disorders
 
PDX Collection 6621
K3189Other diseases of stomach and duodenum
K319Disease of stomach and duodenum, unspecified
K35200Acute appendicitis with generalized peritonitis, without perforation or abscess
K35201Acute appendicitis with generalized peritonitis, with perforation, without abscess
K35209Acute appendicitis with generalized peritonitis, without abscess, unspecified as to perforation
K35210Acute appendicitis with generalized peritonitis, without perforation, with abscess
K35211Acute appendicitis with generalized peritonitis, with perforation and abscess
K35219Acute appendicitis with generalized peritonitis, with abscess, unspecified as to perforation
K3530Acute appendicitis with localized peritonitis, without perforation or gangrene
K3531Acute appendicitis with localized peritonitis and gangrene, without perforation
K3532Acute appendicitis with perforation, localized peritonitis, and gangrene, without abscess
K3533Acute appendicitis with perforation, localized peritonitis, and gangrene, with abscess
K3580Unspecified acute appendicitis
K35890Other acute appendicitis without perforation or gangrene
K35891Other acute appendicitis without perforation, with gangrene
K36Other appendicitis
K37Unspecified appendicitis
K380Hyperplasia of appendix
K381Appendicular concretions
K382Diverticulum of appendix
K383Fistula of appendix
K388Other specified diseases of appendix
K389Disease of appendix, unspecified
K9281Gastrointestinal mucositis (ulcerative)
 
PDX Collection 6622
G041Tropical spastic paraplegia
G10Huntington's disease
G110Congenital nonprogressive ataxia
G1110Early-onset cerebellar ataxia, unspecified
G1111Friedreich ataxia
G1119Other early-onset cerebellar ataxia
G112Late-onset cerebellar ataxia
G113Cerebellar ataxia with defective DNA repair
G114Hereditary spastic paraplegia
G115Hypomyelination - hypogonadotropic hypogonadism - hypodontia
G116Leukodystrophy with vanishing white matter disease
G118Other hereditary ataxias
G119Hereditary ataxia, unspecified
G120Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
G121Other inherited spinal muscular atrophy
G1220Motor neuron disease, unspecified
G1221Amyotrophic lateral sclerosis
G1222Progressive bulbar palsy
G1223Primary lateral sclerosis
G1224Familial motor neuron disease
G1225Progressive spinal muscle atrophy
G1229Other motor neuron disease
G128Other spinal muscular atrophies and related syndromes
G129Spinal muscular atrophy, unspecified
G210Malignant neuroleptic syndrome
G230Hallervorden-Spatz disease
G231Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski]
G232Striatonigral degeneration
G233Hypomyelination with atrophy of the basal ganglia and cerebellum
G238Other specified degenerative diseases of basal ganglia
G239Degenerative disease of basal ganglia, unspecified
G2401Drug induced subacute dyskinesia
G2402Drug induced acute dystonia
G2409Other drug induced dystonia
G241Genetic torsion dystonia
G242Idiopathic nonfamilial dystonia
G243Spasmodic torticollis
G244Idiopathic orofacial dystonia
G245Blepharospasm
G248Other dystonia
G249Dystonia, unspecified
G250Essential tremor
G251Drug-induced tremor



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