DRAFT

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 1262 of 1375
PDX Collection 6646 (continued)
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 6647
A9230West Nile virus infection, unspecified
A9231West Nile virus infection with encephalitis
A9232West Nile virus infection with other neurologic manifestation
A9239West Nile virus infection with other complications
B9721SARS-associated coronavirus as the cause of diseases classified elsewhere
G370Diffuse sclerosis of central nervous system
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9342Megaloencephalic leukoencephalopathy with subcortical cysts
G9343Leukoencephalopathy with calcifications and cysts
G9344Adult-onset leukodystrophy with axonal spheroids
G9349Other encephalopathy
I6783Posterior reversible encephalopathy syndrome
 
PDX Collection 6648
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 6649
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
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
G252Other specified forms of tremor
G253Myoclonus
G254Drug-induced chorea
G255Other chorea
G2561Drug induced tics
G2569Other tics of organic origin
G2570Drug induced movement disorder, unspecified
G2571Drug induced akathisia
G2579Other drug induced movement disorders
G2582Stiff-man syndrome
G2583Benign shuddering attacks
G2589Other specified extrapyramidal and movement disorders
G259Extrapyramidal and movement disorder, unspecified
G26Extrapyramidal and movement disorders in diseases classified elsewhere
G320Subacute combined degeneration of spinal cord in diseases classified elsewhere
G3281Cerebellar ataxia in diseases classified elsewhere
G3289Other specified degenerative disorders of nervous system in diseases classified elsewhere
G35Multiple sclerosis
G360Neuromyelitis optica [Devic]
G361Acute and subacute hemorrhagic leukoencephalitis [Hurst]
G368Other specified acute disseminated demyelination
G369Acute disseminated demyelination, unspecified
G370Diffuse sclerosis of central nervous system
G371Central demyelination of corpus callosum
G372Central pontine myelinolysis
G373Acute transverse myelitis in demyelinating disease of central nervous system
G375Concentric sclerosis [Balo] of central nervous system
G3781Myelin oligodendrocyte glycoprotein antibody disease
G3789Other specified demyelinating diseases of central nervous system
G379Demyelinating disease of central nervous system, unspecified
G800Spastic quadriplegic cerebral palsy
G801Spastic diplegic cerebral palsy
G802Spastic hemiplegic cerebral palsy
G803Athetoid cerebral palsy
G804Ataxic cerebral palsy
G808Other cerebral palsy
G809Cerebral palsy, unspecified
G8100Flaccid hemiplegia affecting unspecified side
G8101Flaccid hemiplegia affecting right dominant side
G8102Flaccid hemiplegia affecting left dominant side
G8103Flaccid hemiplegia affecting right nondominant side
G8104Flaccid hemiplegia affecting left nondominant side
G8110Spastic hemiplegia affecting unspecified side
G8111Spastic hemiplegia affecting right dominant side
G8112Spastic hemiplegia affecting left dominant side
G8113Spastic hemiplegia affecting right nondominant side
G8114Spastic hemiplegia affecting left nondominant side
G8190Hemiplegia, unspecified affecting unspecified side
G8191Hemiplegia, unspecified affecting right dominant side
G8192Hemiplegia, unspecified affecting left dominant side
G8193Hemiplegia, unspecified affecting right nondominant side
G8194Hemiplegia, unspecified affecting left nondominant side
G8220Paraplegia, unspecified
G8221Paraplegia, complete
G8222Paraplegia, incomplete
G8250Quadriplegia, unspecified
G8251Quadriplegia, C1-C4 complete
G8252Quadriplegia, C1-C4 incomplete
G8253Quadriplegia, C5-C7 complete
G8254Quadriplegia, C5-C7 incomplete
G830Diplegia of upper limbs
G8310Monoplegia of lower limb affecting unspecified side
G8311Monoplegia of lower limb affecting right dominant side
G8312Monoplegia of lower limb affecting left dominant side
G8313Monoplegia of lower limb affecting right nondominant side
G8314Monoplegia of lower limb affecting left nondominant side
G8320Monoplegia of upper limb affecting unspecified side
G8321Monoplegia of upper limb affecting right dominant side
G8322Monoplegia of upper limb affecting left dominant side
G8323Monoplegia of upper limb affecting right nondominant side
G8324Monoplegia of upper limb affecting left nondominant side
G8330Monoplegia, unspecified affecting unspecified side
G8331Monoplegia, unspecified affecting right dominant side
G8332Monoplegia, unspecified affecting left dominant side
G8333Monoplegia, unspecified affecting right nondominant side
G8334Monoplegia, unspecified affecting left nondominant side
G834Cauda equina syndrome
G835Locked-in state
G8381Brown-Sequard syndrome
G8382Anterior cord syndrome
G8383Posterior cord syndrome
G8384Todd's paralysis (postepileptic)
G8389Other specified paralytic syndromes
G839Paralytic syndrome, unspecified
G9001Carotid sinus syncope
G9009Other idiopathic peripheral autonomic neuropathy
G902Horner's syndrome
G904Autonomic dysreflexia
G9050Complex regional pain syndrome I, unspecified
G90511Complex regional pain syndrome I of right upper limb
G90512Complex regional pain syndrome I of left upper limb
G90513Complex regional pain syndrome I of upper limb, bilateral
G90519Complex regional pain syndrome I of unspecified upper limb
G90521Complex regional pain syndrome I of right lower limb
G90522Complex regional pain syndrome I of left lower limb
G90523Complex regional pain syndrome I of lower limb, bilateral
G90529Complex regional pain syndrome I of unspecified lower limb
G9059Complex regional pain syndrome I of other specified site
G908Other disorders of autonomic nervous system
G909Disorder of the autonomic nervous system, unspecified
G90BLMNB1-related autosomal dominant leukodystrophy
G9340Encephalopathy, unspecified
G9341Metabolic encephalopathy
G9342Megaloencephalic leukoencephalopathy with subcortical cysts
G9343Leukoencephalopathy with calcifications and cysts
G9344Adult-onset leukodystrophy with axonal spheroids
G9349Other encephalopathy
G9381Temporal sclerosis
G9389Other specified disorders of brain
G939Disorder of brain, unspecified
G950Syringomyelia and syringobulbia
G9511Acute infarction of spinal cord (embolic) (nonembolic)
G9519Other vascular myelopathies
G9520Unspecified cord compression
G9529Other cord compression
G9581Conus medullaris syndrome
G9589Other specified diseases of spinal cord
G959Disease of spinal cord, unspecified
G969Disorder of central nervous system, unspecified
G980Neurogenic arthritis, not elsewhere classified



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