DRAFT

ICD-10-CM/PCS MS-DRG v40.0 Definitions Manual

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Appendix C: Principal diagnoses which convert CC/MCC to non-CC
Page 48 of 1270
PDX Collection 0535 (continued)
E8840Mitochondrial metabolism disorder, unspecified
E8841MELAS syndrome
E8842MERRF syndrome
E8849Other mitochondrial metabolism disorders
E8889Other specified metabolic disorders
H49811Kearns-Sayre syndrome, right eye
H49812Kearns-Sayre syndrome, left eye
H49813Kearns-Sayre syndrome, bilateral
H49819Kearns-Sayre syndrome, unspecified eye
 
PDX Collection 0536
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
E71548Other peroxisomal disorders
E803Defects of catalase and peroxidase
E804Gilbert syndrome
E805Crigler-Najjar syndrome
E806Other disorders of bilirubin metabolism
E807Disorder of bilirubin metabolism, unspecified
E8840Mitochondrial metabolism disorder, unspecified
E8841MELAS syndrome
E8842MERRF syndrome
E8849Other mitochondrial metabolism disorders
E8889Other specified metabolic disorders
H49811Kearns-Sayre syndrome, right eye
H49812Kearns-Sayre syndrome, left eye
H49813Kearns-Sayre syndrome, bilateral
H49819Kearns-Sayre syndrome, unspecified eye
 
PDX Collection 0537
E7500GM2 gangliosidosis, unspecified
E7501Sandhoff disease
E7502Tay-Sachs disease
E7509Other GM2 gangliosidosis
E7510Unspecified gangliosidosis
E7511Mucolipidosis IV
E7519Other gangliosidosis
E754Neuronal ceroid lipofuscinosis
F842Rett's syndrome
G132Systemic atrophy primarily affecting the central nervous system in myxedema
G138Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere
G300Alzheimer's disease with early onset
G301Alzheimer's disease with late onset
G308Other Alzheimer's disease
G309Alzheimer's disease, unspecified
G3101Pick's disease
G3109Other frontotemporal neurocognitive disorder
G311Senile degeneration of brain, not elsewhere classified
G312Degeneration of nervous system due to alcohol
G3181Alpers disease
G3182Leigh's disease
G3184Mild cognitive impairment of uncertain or unknown etiology
G3185Corticobasal degeneration
G3189Other specified degenerative diseases of nervous system
G319Degenerative disease of nervous system, unspecified
G914Hydrocephalus in diseases classified elsewhere
G94Other disorders of brain in diseases classified elsewhere
 
PDX Collection 0538
E7500GM2 gangliosidosis, unspecified
E7501Sandhoff disease
E7502Tay-Sachs disease
E7509Other GM2 gangliosidosis
E7510Unspecified gangliosidosis
E7511Mucolipidosis IV
E7519Other gangliosidosis
E7523Krabbe disease
E7525Metachromatic leukodystrophy
E7526Sulfatase deficiency
E7529Other sphingolipidosis
E754Neuronal ceroid lipofuscinosis
F842Rett's syndrome
G132Systemic atrophy primarily affecting the central nervous system in myxedema
G138Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere
G312Degeneration of nervous system due to alcohol
G3181Alpers disease
G3182Leigh's disease
G3289Other specified degenerative disorders of nervous system in diseases classified elsewhere
G914Hydrocephalus in diseases classified elsewhere
G9381Temporal sclerosis
G9389Other specified disorders of brain
G939Disorder of brain, unspecified
G94Other disorders of brain in diseases classified elsewhere
G969Disorder of central nervous system, unspecified
G980Neurogenic arthritis, not elsewhere classified
G988Other disorders of nervous system
G998Other specified disorders of nervous system in diseases classified elsewhere
 
PDX Collection 0539
D8130Adenosine deaminase deficiency, unspecified
D8131Severe combined immunodeficiency due to adenosine deaminase deficiency
D8132Adenosine deaminase 2 deficiency
D8139Other adenosine deaminase deficiency
D815Purine nucleoside phosphorylase [PNP] deficiency
D81810Biotinidase deficiency
D841Defects in the complement system
E7601Hurler's syndrome
E7602Hurler-Scheie syndrome
E7603Scheie's syndrome
E761Mucopolysaccharidosis, type II
E76210Morquio A mucopolysaccharidoses
E76211Morquio B mucopolysaccharidoses
E76219Morquio mucopolysaccharidoses, unspecified
E7622Sanfilippo mucopolysaccharidoses
E7629Other mucopolysaccharidoses
E763Mucopolysaccharidosis, unspecified
E768Other disorders of glucosaminoglycan metabolism
E769Glucosaminoglycan metabolism disorder, unspecified
E791Lesch-Nyhan syndrome
E792Myoadenylate deaminase deficiency
E798Other disorders of purine and pyrimidine metabolism
E799Disorder of purine and pyrimidine metabolism, unspecified
E800Hereditary erythropoietic porphyria
E801Porphyria cutanea tarda
E8020Unspecified porphyria
E8021Acute intermittent (hepatic) porphyria
E8029Other porphyria
E804Gilbert syndrome
E805Crigler-Najjar syndrome
E806Other disorders of bilirubin metabolism
E807Disorder of bilirubin metabolism, unspecified
E850Non-neuropathic heredofamilial amyloidosis
E859Amyloidosis, unspecified
E8881Metabolic syndrome
 
PDX Collection 0540
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
Q872Congenital malformation syndromes predominantly involving limbs
Q873Congenital malformation syndromes involving early overgrowth
Q8740Marfan's syndrome, unspecified
Q87410Marfan's syndrome with aortic dilation
Q87418Marfan's syndrome with other cardiovascular manifestations
Q8742Marfan's syndrome with ocular manifestations
Q8743Marfan's syndrome with skeletal manifestation
Q875Other congenital malformation syndromes with other skeletal changes
Q8781Alport syndrome
Q8782Arterial tortuosity syndrome
Q8789Other specified congenital malformation syndromes, not elsewhere classified
Q898Other specified congenital malformations
Q992Fragile X chromosome
 
PDX Collection 0541
E840Cystic fibrosis with pulmonary manifestations
E8411Meconium ileus in cystic fibrosis
E8419Cystic fibrosis with other intestinal manifestations
E848Cystic fibrosis with other manifestations
E849Cystic fibrosis, unspecified
 
PDX Collection 0542
E850Non-neuropathic heredofamilial amyloidosis
E851Neuropathic heredofamilial amyloidosis
E852Heredofamilial amyloidosis, unspecified
E853Secondary systemic amyloidosis
E854Organ-limited amyloidosis
E8581Light chain (AL) amyloidosis
E8582Wild-type transthyretin-related (ATTR) amyloidosis
E8589Other amyloidosis
E859Amyloidosis, unspecified
E8881Metabolic syndrome
 
PDX Collection 0545
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
E8889Other specified metabolic disorders
H49819Kearns-Sayre syndrome, unspecified eye
 
PDX Collection 0546
E368Other intraoperative complications of endocrine system
E89810Postprocedural hemorrhage of an endocrine system organ or structure following an endocrine system procedure
E89811Postprocedural hemorrhage of an endocrine system organ or structure following other procedure
E89820Postprocedural hematoma of an endocrine system organ or structure following an endocrine system procedure
E89821Postprocedural hematoma of an endocrine system organ or structure following other procedure
E89822Postprocedural seroma of an endocrine system organ or structure following an endocrine system procedure
E89823Postprocedural seroma of an endocrine system organ or structure following other procedure
E8989Other postprocedural endocrine and metabolic complications and disorders
H95811Postprocedural stenosis of right external ear canal
H95812Postprocedural stenosis of left external ear canal
H95813Postprocedural stenosis of external ear canal, bilateral
H95819Postprocedural stenosis of unspecified external ear canal
H9588Other intraoperative complications and disorders of the ear and mastoid process, not elsewhere classified
H9589Other postprocedural complications and disorders of the ear and mastoid process, not elsewhere classified
I973Postprocedural hypertension
M9689Other intraoperative and postprocedural complications and disorders of the musculoskeletal system
N981Hyperstimulation of ovaries
N982Complications of attempted introduction of fertilized ovum following in vitro fertilization
N983Complications of attempted introduction of embryo in embryo transfer
N988Other complications associated with artificial fertilization
N989Complication associated with artificial fertilization, unspecified
T8182XAEmphysema (subcutaneous) resulting from a procedure, initial encounter
T8189XAOther complications of procedures, not elsewhere classified, initial encounter
T819XXAUnspecified complication of procedure, initial encounter
 
PDX Collection 0549
F05Delirium due to known physiological condition
R45851Suicidal ideations
 
PDX Collection 0553
F3113Bipolar disorder, current episode manic without psychotic features, severe
F312Bipolar disorder, current episode manic severe with psychotic features
F3163Bipolar disorder, current episode mixed, severe, without psychotic features
F3164Bipolar disorder, current episode mixed, severe, with psychotic features
 
PDX Collection 0554
F3113Bipolar disorder, current episode manic without psychotic features, severe
F312Bipolar disorder, current episode manic severe with psychotic features
F314Bipolar disorder, current episode depressed, severe, without psychotic features
F315Bipolar disorder, current episode depressed, severe, with psychotic features
F3163Bipolar disorder, current episode mixed, severe, without psychotic features
F3164Bipolar disorder, current episode mixed, severe, with psychotic features
 
PDX Collection 0556
F459Somatoform disorder, unspecified
F5000Anorexia nervosa, unspecified
F5001Anorexia nervosa, restricting type
F5002Anorexia nervosa, binge eating/purging type
F502Bulimia nervosa
F5081Binge eating disorder
F5082Avoidant/restrictive food intake disorder
F5089Other specified eating disorder
F509Eating disorder, unspecified
F59Unspecified behavioral syndromes associated with physiological disturbances and physical factors
F9821Rumination disorder of infancy
F9829Other feeding disorders of infancy and early childhood
F983Pica of infancy and childhood
 
PDX Collection 0557
F5000Anorexia nervosa, unspecified
F5001Anorexia nervosa, restricting type
F5002Anorexia nervosa, binge eating/purging type
F502Bulimia nervosa
F5081Binge eating disorder
F5082Avoidant/restrictive food intake disorder
F5089Other specified eating disorder
F509Eating disorder, unspecified
F9821Rumination disorder of infancy
F9829Other feeding disorders of infancy and early childhood
 
PDX Collection 0558
F72Severe intellectual disabilities
F73Profound intellectual disabilities
 
PDX Collection 0559
A0221Salmonella meningitis
A170Tuberculous meningitis
A171Meningeal tuberculoma
A2781Aseptic meningitis in leptospirosis
A390Meningococcal meningitis
A5041Late congenital syphilitic meningitis
A5141Secondary syphilitic meningitis
A5213Late syphilitic meningitis
A5482Gonococcal brain abscess
A5484Gonococcal pneumonia
A5489Other gonococcal infections
A549Gonococcal infection, unspecified
A870Enteroviral meningitis
A871Adenoviral meningitis
A872Lymphocytic choriomeningitis
A878Other viral meningitis
A879Viral meningitis, unspecified
B003Herpesviral meningitis
B021Zoster meningitis
B261Mumps meningitis
B375Candidal meningitis
B384Coccidioidomycosis meningitis
B451Cerebral cryptococcosis
B582Toxoplasma meningoencephalitis
G000Hemophilus meningitis
G001Pneumococcal meningitis
G002Streptococcal meningitis
G003Staphylococcal meningitis
G008Other bacterial meningitis
G009Bacterial meningitis, unspecified
G01Meningitis in bacterial diseases classified elsewhere
G02Meningitis in other infectious and parasitic diseases classified elsewhere
G030Nonpyogenic meningitis
G031Chronic meningitis
G032Benign recurrent meningitis [Mollaret]
G038Meningitis due to other specified causes
G039Meningitis, unspecified
G042Bacterial meningoencephalitis and meningomyelitis, not elsewhere classified
G3289Other specified degenerative disorders of nervous system in diseases classified elsewhere
G610Guillain-Barre syndrome
G969Disorder of central nervous system, unspecified
G980Neurogenic arthritis, not elsewhere classified
G988Other disorders of nervous system
G998Other specified disorders of nervous system in diseases classified elsewhere
 
PDX Collection 0560
A0221Salmonella meningitis
A170Tuberculous meningitis
A171Meningeal tuberculoma
A1782Tuberculous meningoencephalitis
A2781Aseptic meningitis in leptospirosis
A390Meningococcal meningitis
A5041Late congenital syphilitic meningitis
A5042Late congenital syphilitic encephalitis
A5141Secondary syphilitic meningitis
A5213Late syphilitic meningitis
A5214Late syphilitic encephalitis
A5482Gonococcal brain abscess
A5484Gonococcal pneumonia
A5489Other gonococcal infections
A549Gonococcal infection, unspecified
A811Subacute sclerosing panencephalitis
A8182Gerstmann-Straussler-Scheinker syndrome
A8183Fatal familial insomnia
A8189Other atypical virus infections of central nervous system
A830Japanese encephalitis
A831Western equine encephalitis
A832Eastern equine encephalitis
A833St Louis encephalitis
A834Australian encephalitis
A835California encephalitis
A836Rocio virus disease
A838Other mosquito-borne viral encephalitis
A839Mosquito-borne viral encephalitis, unspecified
A840Far Eastern tick-borne encephalitis [Russian spring-summer encephalitis]
A841Central European tick-borne encephalitis
A8481Powassan virus disease
A8489Other tick-borne viral encephalitis
A849Tick-borne viral encephalitis, unspecified
A850Enteroviral encephalitis
A851Adenoviral encephalitis
A852Arthropod-borne viral encephalitis, unspecified
A858Other specified viral encephalitis
A870Enteroviral meningitis
A871Adenoviral meningitis
A872Lymphocytic choriomeningitis
A878Other viral meningitis
A879Viral meningitis, unspecified
A880Enteroviral exanthematous fever [Boston exanthem]
A888Other specified viral infections of central nervous system
A921O'nyong-nyong fever
A922Venezuelan equine fever
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
A924Rift Valley fever
A925Zika virus disease
A928Other specified mosquito-borne viral fevers
A930Oropouche virus disease
A962Lassa fever
A983Marburg virus disease
A984Ebola virus disease
B003Herpesviral meningitis
B004Herpesviral encephalitis
B0089Other herpesviral infection
B009Herpesviral infection, unspecified
B010Varicella meningitis
B0111Varicella encephalitis and encephalomyelitis
B0181Varicella keratitis
B0189Other varicella complications
B019Varicella without complication
B020Zoster encephalitis
B021Zoster meningitis
B0221Postherpetic geniculate ganglionitis
B0222Postherpetic trigeminal neuralgia
B0223Postherpetic polyneuropathy
B0229Other postherpetic nervous system involvement
B027Disseminated zoster
B028Zoster with other complications
B029Zoster without complications
B04Monkeypox
B0601Rubella encephalitis
B0804Paravaccinia, unspecified
B0809Other orthopoxvirus infections
B0820Exanthema subitum [sixth disease], unspecified
B0821Exanthema subitum [sixth disease] due to human herpesvirus 6
B0822Exanthema subitum [sixth disease] due to human herpesvirus 7
B0860Parapoxvirus infection, unspecified
B0861Bovine stomatitis
B0862Sealpox
B0869Other parapoxvirus infections
B0870Yatapoxvirus infection, unspecified
B0871Tanapox virus disease
B0872Yaba pox virus disease
B0879Other yatapoxvirus infections
B09Unspecified viral infection characterized by skin and mucous membrane lesions
B1001Human herpesvirus 6 encephalitis
B1009Other human herpesvirus encephalitis
B1081Human herpesvirus 6 infection
B1082Human herpesvirus 7 infection
B1089Other human herpesvirus infection
B261Mumps meningitis
B262Mumps encephalitis
B2700Gammaherpesviral mononucleosis without complication



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