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 1128 of 1324
PDX Collection 6239 (continued)
J698Pneumonitis due to inhalation of other solids and liquids
J700Acute pulmonary manifestations due to radiation
J701Chronic and other pulmonary manifestations due to radiation
J702Acute drug-induced interstitial lung disorders
J703Chronic drug-induced interstitial lung disorders
J704Drug-induced interstitial lung disorders, unspecified
J708Respiratory conditions due to other specified external agents
J709Respiratory conditions due to unspecified external agent
J984Other disorders of lung
J988Other specified respiratory disorders
J989Respiratory disorder, unspecified
N80B1Endometriosis of pleura
N80B2Endometriosis of lung
N80B31Superficial endometriosis of diaphragm
N80B32Deep endometriosis of diaphragm
N80B39Endometriosis of diaphragm, unspecified depth
R911Solitary pulmonary nodule
 
PDX Collection 6240
D800Hereditary hypogammaglobulinemia
D803Selective deficiency of immunoglobulin G [IgG] subclasses
D804Selective deficiency of immunoglobulin M [IgM]
D805Immunodeficiency with increased immunoglobulin M [IgM]
D806Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
D807Transient hypogammaglobulinemia of infancy
D808Other immunodeficiencies with predominantly antibody defects
D809Immunodeficiency with predominantly antibody defects, unspecified
D810Severe combined immunodeficiency [SCID] with reticular dysgenesis
D811Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
D812Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
D814Nezelof's syndrome
D816Major histocompatibility complex class I deficiency
D817Major histocompatibility complex class II deficiency
D8182Activated Phosphoinositide 3-kinase Delta Syndrome [APDS]
D8189Other combined immunodeficiencies
D819Combined immunodeficiency, unspecified
D820Wiskott-Aldrich syndrome
D821Di George's syndrome
D822Immunodeficiency with short-limbed stature
D823Immunodeficiency following hereditary defective response to Epstein-Barr virus
D824Hyperimmunoglobulin E [IgE] syndrome
D828Immunodeficiency associated with other specified major defects
D829Immunodeficiency associated with major defect, unspecified
D830Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
D831Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
D832Common variable immunodeficiency with autoantibodies to B- or T-cells
D838Other common variable immunodeficiencies
D839Common variable immunodeficiency, unspecified
D840Lymphocyte function antigen-1 [LFA-1] defect
D84821Immunodeficiency due to drugs
D84822Immunodeficiency due to external causes
D8489Other immunodeficiencies
D849Immunodeficiency, unspecified
D893Immune reconstitution syndrome
D8940Mast cell activation, unspecified
D8941Monoclonal mast cell activation syndrome
D8942Idiopathic mast cell activation syndrome
D8943Secondary mast cell activation
D8949Other mast cell activation disorder
D8982Autoimmune lymphoproliferative syndrome [ALPS]
D8984IgG4-related disease
D8989Other specified disorders involving the immune mechanism, not elsewhere classified
D899Disorder involving the immune mechanism, unspecified
 
PDX Collection 6241
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
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
E804Gilbert syndrome
E805Crigler-Najjar syndrome
E806Other disorders of bilirubin metabolism
E807Disorder of bilirubin metabolism, unspecified
E8840Mitochondrial metabolism disorder, unspecified
E8841MELAS syndrome
E8842MERRF syndrome
E8843Disorders of mitochondrial tRNA synthetases
E8849Other mitochondrial metabolism disorders
H49811Kearns-Sayre syndrome, right eye
H49812Kearns-Sayre syndrome, left eye
H49813Kearns-Sayre syndrome, bilateral
H49819Kearns-Sayre syndrome, unspecified eye
 
PDX Collection 6242
D800Hereditary hypogammaglobulinemia
D803Selective deficiency of immunoglobulin G [IgG] subclasses
D804Selective deficiency of immunoglobulin M [IgM]
D805Immunodeficiency with increased immunoglobulin M [IgM]
D806Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
D807Transient hypogammaglobulinemia of infancy
D808Other immunodeficiencies with predominantly antibody defects
D809Immunodeficiency with predominantly antibody defects, unspecified
D810Severe combined immunodeficiency [SCID] with reticular dysgenesis
D811Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
D812Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
D814Nezelof's syndrome
D816Major histocompatibility complex class I deficiency
D817Major histocompatibility complex class II deficiency
D8182Activated Phosphoinositide 3-kinase Delta Syndrome [APDS]
D8189Other combined immunodeficiencies
D819Combined immunodeficiency, unspecified
D820Wiskott-Aldrich syndrome
D821Di George's syndrome
D822Immunodeficiency with short-limbed stature
D823Immunodeficiency following hereditary defective response to Epstein-Barr virus
D824Hyperimmunoglobulin E [IgE] syndrome
D828Immunodeficiency associated with other specified major defects
D829Immunodeficiency associated with major defect, unspecified
D830Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
D831Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
D832Common variable immunodeficiency with autoantibodies to B- or T-cells
D838Other common variable immunodeficiencies
D839Common variable immunodeficiency, unspecified
D840Lymphocyte function antigen-1 [LFA-1] defect
D84821Immunodeficiency due to drugs
D84822Immunodeficiency due to external causes
D8489Other immunodeficiencies
D849Immunodeficiency, unspecified
D893Immune reconstitution syndrome
D8940Mast cell activation, unspecified
D8941Monoclonal mast cell activation syndrome
D8942Idiopathic mast cell activation syndrome
D8943Secondary mast cell activation
D8949Other mast cell activation disorder
D8982Autoimmune lymphoproliferative syndrome [ALPS]
D8984IgG4-related disease
D8989Other specified disorders involving the immune mechanism, not elsewhere classified
D899Disorder involving the immune mechanism, unspecified
 
PDX Collection 6243
C965Multifocal and unisystemic 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
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
E804Gilbert syndrome
E805Crigler-Najjar syndrome
E806Other disorders of bilirubin metabolism
E807Disorder of bilirubin metabolism, unspecified
E8840Mitochondrial metabolism disorder, unspecified
E8841MELAS syndrome
E8842MERRF syndrome
E8843Disorders of mitochondrial tRNA synthetases
E8849Other mitochondrial metabolism disorders
H49811Kearns-Sayre syndrome, right eye
H49812Kearns-Sayre syndrome, left eye
H49813Kearns-Sayre syndrome, bilateral
H49819Kearns-Sayre syndrome, unspecified eye
 
PDX Collection 6244
A150Tuberculosis of lung
A154Tuberculosis of intrathoracic lymph nodes
A155Tuberculosis of larynx, trachea and bronchus
A156Tuberculous pleurisy
A158Other respiratory tuberculosis
A159Respiratory tuberculosis unspecified
A179Tuberculosis of nervous system, unspecified
A1882Tuberculosis of other endocrine glands
A1884Tuberculosis of heart
A1889Tuberculosis of other sites
A202Pneumonic plague
A211Oculoglandular tularemia
A221Pulmonary anthrax
A310Pulmonary mycobacterial infection
A3701Whooping cough due to Bordetella pertussis with pneumonia
A3711Whooping cough due to Bordetella parapertussis with pneumonia
A3781Whooping cough due to other Bordetella species with pneumonia
A3791Whooping cough, unspecified species with pneumonia
A420Pulmonary actinomycosis
A430Pulmonary nocardiosis
A481Legionnaires' disease
B250Cytomegaloviral pneumonitis
B390Acute pulmonary histoplasmosis capsulati
B391Chronic pulmonary histoplasmosis capsulati
B392Pulmonary histoplasmosis capsulati, unspecified
B440Invasive pulmonary aspergillosis
B583Pulmonary toxoplasmosis
B59Pneumocystosis
B671Echinococcus granulosus infection of lung
J09X1Influenza due to identified novel influenza A virus with pneumonia
J09X2Influenza due to identified novel influenza A virus with other respiratory manifestations
J1000Influenza due to other identified influenza virus with unspecified type of pneumonia
J1001Influenza due to other identified influenza virus with the same other identified influenza virus pneumonia
J1008Influenza due to other identified influenza virus with other specified pneumonia
J101Influenza due to other identified influenza virus with other respiratory manifestations
J1100Influenza due to unidentified influenza virus with unspecified type of pneumonia
J1108Influenza due to unidentified influenza virus with specified pneumonia
J111Influenza due to unidentified influenza virus with other respiratory manifestations
J120Adenoviral pneumonia
J121Respiratory syncytial virus pneumonia
J122Parainfluenza virus pneumonia
J123Human metapneumovirus pneumonia
J1281Pneumonia due to SARS-associated coronavirus
J1289Other viral pneumonia
J129Viral pneumonia, unspecified
J13Pneumonia due to Streptococcus pneumoniae
J14Pneumonia due to Hemophilus influenzae
J150Pneumonia due to Klebsiella pneumoniae
J151Pneumonia due to Pseudomonas
J1520Pneumonia due to staphylococcus, unspecified
J15211Pneumonia due to Methicillin susceptible Staphylococcus aureus
J15212Pneumonia due to Methicillin resistant Staphylococcus aureus
J1529Pneumonia due to other staphylococcus
J153Pneumonia due to streptococcus, group B
J154Pneumonia due to other streptococci
J155Pneumonia due to Escherichia coli
J1561Pneumonia due to Acinetobacter baumannii
J1569Pneumonia due to other Gram-negative bacteria
J157Pneumonia due to Mycoplasma pneumoniae
J158Pneumonia due to other specified bacteria
J159Unspecified bacterial pneumonia
J160Chlamydial pneumonia
J168Pneumonia due to other specified infectious organisms
J180Bronchopneumonia, unspecified organism
J181Lobar pneumonia, unspecified organism
J188Other pneumonia, unspecified organism
J189Pneumonia, unspecified organism
J22Unspecified acute lower respiratory infection
J60Coalworker's pneumoconiosis
J61Pneumoconiosis due to asbestos and other mineral fibers
J620Pneumoconiosis due to talc dust
J628Pneumoconiosis due to other dust containing silica
J630Aluminosis (of lung)
J631Bauxite fibrosis (of lung)
J632Berylliosis
J633Graphite fibrosis (of lung)
J634Siderosis
J635Stannosis
J636Pneumoconiosis due to other specified inorganic dusts
J64Unspecified pneumoconiosis
J65Pneumoconiosis associated with tuberculosis
J660Byssinosis
J661Flax-dressers' disease
J662Cannabinosis
J668Airway disease due to other specific organic dusts
J670Farmer's lung
J671Bagassosis
J672Bird fancier's lung
J673Suberosis
J674Maltworker's lung
J675Mushroom-worker's lung
J676Maple-bark-stripper's lung
J677Air conditioner and humidifier lung
J678Hypersensitivity pneumonitis due to other organic dusts
J679Hypersensitivity pneumonitis due to unspecified organic dust
J680Bronchitis and pneumonitis due to chemicals, gases, fumes and vapors
J681Pulmonary edema due to chemicals, gases, fumes and vapors
J682Upper respiratory inflammation due to chemicals, gases, fumes and vapors, not elsewhere classified
J683Other acute and subacute respiratory conditions due to chemicals, gases, fumes and vapors
J684Chronic respiratory conditions due to chemicals, gases, fumes and vapors
J688Other respiratory conditions due to chemicals, gases, fumes and vapors
J689Unspecified respiratory condition due to chemicals, gases, fumes and vapors
J690Pneumonitis due to inhalation of food and vomit
J691Pneumonitis due to inhalation of oils and essences
J698Pneumonitis due to inhalation of other solids and liquids
J700Acute pulmonary manifestations due to radiation
J701Chronic and other pulmonary manifestations due to radiation
J702Acute drug-induced interstitial lung disorders
J703Chronic drug-induced interstitial lung disorders
J704Drug-induced interstitial lung disorders, unspecified
J708Respiratory conditions due to other specified external agents
J709Respiratory conditions due to unspecified external agent
J984Other disorders of lung
J988Other specified respiratory disorders
J989Respiratory disorder, unspecified
N80B1Endometriosis of pleura
N80B2Endometriosis of lung
N80B31Superficial endometriosis of diaphragm
N80B32Deep endometriosis of diaphragm
N80B39Endometriosis of diaphragm, unspecified depth
R911Solitary pulmonary nodule
 
PDX Collection 6245
D800Hereditary hypogammaglobulinemia
D803Selective deficiency of immunoglobulin G [IgG] subclasses
D804Selective deficiency of immunoglobulin M [IgM]
D805Immunodeficiency with increased immunoglobulin M [IgM]
D806Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
D807Transient hypogammaglobulinemia of infancy
D808Other immunodeficiencies with predominantly antibody defects
D809Immunodeficiency with predominantly antibody defects, unspecified
D810Severe combined immunodeficiency [SCID] with reticular dysgenesis
D811Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
D812Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
D814Nezelof's syndrome
D816Major histocompatibility complex class I deficiency
D817Major histocompatibility complex class II deficiency
D8182Activated Phosphoinositide 3-kinase Delta Syndrome [APDS]
D8189Other combined immunodeficiencies
D819Combined immunodeficiency, unspecified
D820Wiskott-Aldrich syndrome
D821Di George's syndrome
D822Immunodeficiency with short-limbed stature
D823Immunodeficiency following hereditary defective response to Epstein-Barr virus
D824Hyperimmunoglobulin E [IgE] syndrome
D828Immunodeficiency associated with other specified major defects
D829Immunodeficiency associated with major defect, unspecified
D830Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
D831Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
D832Common variable immunodeficiency with autoantibodies to B- or T-cells
D838Other common variable immunodeficiencies
D839Common variable immunodeficiency, unspecified
D840Lymphocyte function antigen-1 [LFA-1] defect
D84821Immunodeficiency due to drugs
D84822Immunodeficiency due to external causes
D8489Other immunodeficiencies
D849Immunodeficiency, unspecified
D893Immune reconstitution syndrome
D8940Mast cell activation, unspecified
D8941Monoclonal mast cell activation syndrome
D8942Idiopathic mast cell activation syndrome
D8943Secondary mast cell activation
D8949Other mast cell activation disorder
D8982Autoimmune lymphoproliferative syndrome [ALPS]
D8984IgG4-related disease
D8989Other specified disorders involving the immune mechanism, not elsewhere classified
D899Disorder involving the immune mechanism, unspecified
 
PDX Collection 6246
D800Hereditary hypogammaglobulinemia
D803Selective deficiency of immunoglobulin G [IgG] subclasses
D804Selective deficiency of immunoglobulin M [IgM]
D805Immunodeficiency with increased immunoglobulin M [IgM]
D806Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia
D807Transient hypogammaglobulinemia of infancy
D808Other immunodeficiencies with predominantly antibody defects
D809Immunodeficiency with predominantly antibody defects, unspecified
D810Severe combined immunodeficiency [SCID] with reticular dysgenesis
D811Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
D812Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
D814Nezelof's syndrome
D816Major histocompatibility complex class I deficiency
D817Major histocompatibility complex class II deficiency
D8182Activated Phosphoinositide 3-kinase Delta Syndrome [APDS]
D8189Other combined immunodeficiencies
D819Combined immunodeficiency, unspecified
D820Wiskott-Aldrich syndrome
D821Di George's syndrome
D822Immunodeficiency with short-limbed stature
D823Immunodeficiency following hereditary defective response to Epstein-Barr virus
D824Hyperimmunoglobulin E [IgE] syndrome
D828Immunodeficiency associated with other specified major defects
D829Immunodeficiency associated with major defect, unspecified
D830Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
D831Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
D832Common variable immunodeficiency with autoantibodies to B- or T-cells
D838Other common variable immunodeficiencies
D839Common variable immunodeficiency, unspecified
D840Lymphocyte function antigen-1 [LFA-1] defect
D84821Immunodeficiency due to drugs
D84822Immunodeficiency due to external causes
D8489Other immunodeficiencies
D849Immunodeficiency, unspecified
D893Immune reconstitution syndrome
D8940Mast cell activation, unspecified
D8941Monoclonal mast cell activation syndrome
D8942Idiopathic mast cell activation syndrome
D8943Secondary mast cell activation
D8949Other mast cell activation disorder
D8982Autoimmune lymphoproliferative syndrome [ALPS]
D8984IgG4-related disease
D8989Other specified disorders involving the immune mechanism, not elsewhere classified
D899Disorder involving the immune mechanism, unspecified



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