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 1300 of 1375
PDX Collection 6821 (continued)
A4901Methicillin susceptible Staphylococcus aureus infection, unspecified site
A4902Methicillin resistant Staphylococcus aureus infection, unspecified site
A491Streptococcal infection, unspecified site
A492Hemophilus influenzae infection, unspecified site
A493Mycoplasma infection, unspecified site
A498Other bacterial infections of unspecified site
A499Bacterial infection, unspecified
A5486Gonococcal sepsis
B007Disseminated herpesviral disease
B377Candidal sepsis
B92Sequelae of leprosy
B942Sequelae of viral hepatitis
B948Sequelae of other specified infectious and parasitic diseases
B949Sequelae of unspecified infectious and parasitic disease
B950Streptococcus, group A, as the cause of diseases classified elsewhere
B951Streptococcus, group B, as the cause of diseases classified elsewhere
B952Enterococcus as the cause of diseases classified elsewhere
B953Streptococcus pneumoniae as the cause of diseases classified elsewhere
B954Other streptococcus as the cause of diseases classified elsewhere
B955Unspecified streptococcus as the cause of diseases classified elsewhere
B9561Methicillin susceptible Staphylococcus aureus infection as the cause of diseases classified elsewhere
B9562Methicillin resistant Staphylococcus aureus infection as the cause of diseases classified elsewhere
B957Other staphylococcus as the cause of diseases classified elsewhere
B958Unspecified staphylococcus as the cause of diseases classified elsewhere
B960Mycoplasma pneumoniae [M. pneumoniae] as the cause of diseases classified elsewhere
B961Klebsiella pneumoniae [K. pneumoniae] as the cause of diseases classified elsewhere
B9620Unspecified Escherichia coli [E. coli] as the cause of diseases classified elsewhere
B9621Shiga toxin-producing Escherichia coli [E. coli] [STEC] O157 as the cause of diseases classified elsewhere
B9622Other specified Shiga toxin-producing Escherichia coli [E. coli] [STEC] as the cause of diseases classified elsewhere
B9623Unspecified Shiga toxin-producing Escherichia coli [E. coli] [STEC] as the cause of diseases classified elsewhere
B9629Other Escherichia coli [E. coli] as the cause of diseases classified elsewhere
B963Hemophilus influenzae [H. influenzae] as the cause of diseases classified elsewhere
B964Proteus (mirabilis) (morganii) as the cause of diseases classified elsewhere
B965Pseudomonas (aeruginosa) (mallei) (pseudomallei) as the cause of diseases classified elsewhere
B966Bacteroides fragilis [B. fragilis] as the cause of diseases classified elsewhere
B967Clostridium perfringens [C. perfringens] as the cause of diseases classified elsewhere
B9681Helicobacter pylori [H. pylori] as the cause of diseases classified elsewhere
B9682Vibrio vulnificus as the cause of diseases classified elsewhere
B9689Other specified bacterial agents as the cause of diseases classified elsewhere
P360Sepsis of newborn due to streptococcus, group B
P3610Sepsis of newborn due to unspecified streptococci
P3619Sepsis of newborn due to other streptococci
P362Sepsis of newborn due to Staphylococcus aureus
P3630Sepsis of newborn due to unspecified staphylococci
P3639Sepsis of newborn due to other staphylococci
P364Sepsis of newborn due to Escherichia coli
P365Sepsis of newborn due to anaerobes
P368Other bacterial sepsis of newborn
P369Bacterial sepsis of newborn, unspecified
P392Intra-amniotic infection affecting newborn, not elsewhere classified
P394Neonatal skin infection
P398Other specified infections specific to the perinatal period
P399Infection specific to the perinatal period, unspecified
R6510Systemic inflammatory response syndrome (SIRS) of non-infectious origin without acute organ dysfunction
R6511Systemic inflammatory response syndrome (SIRS) of non-infectious origin with acute organ dysfunction
R6520Severe sepsis without septic shock
Z1610Resistance to unspecified beta lactam antibiotics
Z1611Resistance to penicillins
Z1612Extended spectrum beta lactamase (ESBL) resistance
Z1619Resistance to other specified beta lactam antibiotics
Z1620Resistance to unspecified antibiotic
Z1621Resistance to vancomycin
Z1622Resistance to vancomycin related antibiotics
Z1623Resistance to quinolones and fluoroquinolones
Z1624Resistance to multiple antibiotics
Z1629Resistance to other single specified antibiotic
Z1630Resistance to unspecified antimicrobial drugs
Z1631Resistance to antiparasitic drug(s)
Z1632Resistance to antifungal drug(s)
Z1633Resistance to antiviral drug(s)
Z16341Resistance to single antimycobacterial drug
Z16342Resistance to multiple antimycobacterial drugs
Z1635Resistance to multiple antimicrobial drugs
Z1639Resistance to other specified antimicrobial drug
 
PDX Collection 6822
G20A1Parkinson's disease without dyskinesia, without mention of fluctuations
G20A2Parkinson's disease without dyskinesia, with fluctuations
G20B1Parkinson's disease with dyskinesia, without mention of fluctuations
G20B2Parkinson's disease with dyskinesia, with fluctuations
G20CParkinsonism, unspecified
G2111Neuroleptic induced parkinsonism
G2119Other drug induced secondary parkinsonism
G212Secondary parkinsonism due to other external agents
G213Postencephalitic parkinsonism
G214Vascular parkinsonism
G218Other secondary parkinsonism
G219Secondary parkinsonism, unspecified
 
PDX Collection 6823
A0100Typhoid fever, unspecified
A0101Typhoid meningitis
A0102Typhoid fever with heart involvement
A0103Typhoid pneumonia
A0104Typhoid arthritis
A0105Typhoid osteomyelitis
A0109Typhoid fever with other complications
A014Paratyphoid fever, unspecified
A020Salmonella enteritis
A039Shigellosis, unspecified
A040Enteropathogenic Escherichia coli infection
A041Enterotoxigenic Escherichia coli infection
A042Enteroinvasive Escherichia coli infection
A043Enterohemorrhagic Escherichia coli infection
A044Other intestinal Escherichia coli infections
A045Campylobacter enteritis
A046Enteritis due to Yersinia enterocolitica
A0471Enterocolitis due to Clostridium difficile, recurrent
A0472Enterocolitis due to Clostridium difficile, not specified as recurrent
A048Other specified bacterial intestinal infections
A049Bacterial intestinal infection, unspecified
A050Foodborne staphylococcal intoxication
A051Botulism food poisoning
A052Foodborne Clostridium perfringens [Clostridium welchii] intoxication
A074Cyclosporiasis
A080Rotaviral enteritis
A0811Acute gastroenteropathy due to Norwalk agent
A0819Acute gastroenteropathy due to other small round viruses
A082Adenoviral enteritis
A0831Calicivirus enteritis
A0832Astrovirus enteritis
A0839Other viral enteritis
A084Viral intestinal infection, unspecified
A088Other specified intestinal infections
A09Infectious gastroenteritis and colitis, unspecified
A4851Infant botulism
A4852Wound botulism
K30Functional dyspepsia
K521Toxic gastroenteritis and colitis
K5221Food protein-induced enterocolitis syndrome
K5222Food protein-induced enteropathy
K5229Other allergic and dietetic gastroenteritis and colitis
K523Indeterminate colitis
K5282Eosinophilic colitis
K52831Collagenous colitis
K52832Lymphocytic colitis
K52838Other microscopic colitis
K52839Microscopic colitis, unspecified
K5289Other specified noninfective gastroenteritis and colitis
K529Noninfective gastroenteritis and colitis, unspecified
K580Irritable bowel syndrome with diarrhea
K581Irritable bowel syndrome with constipation
K582Mixed irritable bowel syndrome
K588Other irritable bowel syndrome
K589Irritable bowel syndrome without diarrhea
K650Generalized (acute) peritonitis
K652Spontaneous bacterial peritonitis
K658Other peritonitis
K6812Psoas muscle abscess
K6819Other retroperitoneal abscess
K682Retroperitoneal fibrosis
K683Retroperitoneal hematoma
K689Other disorders of retroperitoneum
P768Other specified intestinal obstruction of newborn
P769Intestinal obstruction of newborn, unspecified
P771Stage 1 necrotizing enterocolitis in newborn
P772Stage 2 necrotizing enterocolitis in newborn
P773Stage 3 necrotizing enterocolitis in newborn
P779Necrotizing enterocolitis in newborn, unspecified
P781Other neonatal peritonitis
P783Noninfective neonatal diarrhea
P7881Congenital cirrhosis (of liver)
P7882Peptic ulcer of newborn
P7883Newborn esophageal reflux
P7884Gestational alloimmune liver disease
P7889Other specified perinatal digestive system disorders
 
PDX Collection 6824
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
D8481Immunodeficiency due to conditions classified elsewhere
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 6825
G20A1Parkinson's disease without dyskinesia, without mention of fluctuations
G20A2Parkinson's disease without dyskinesia, with fluctuations
G20B1Parkinson's disease with dyskinesia, without mention of fluctuations
G20B2Parkinson's disease with dyskinesia, with fluctuations
G20CParkinsonism, unspecified
G2111Neuroleptic induced parkinsonism
G2119Other drug induced secondary parkinsonism
G212Secondary parkinsonism due to other external agents
G213Postencephalitic parkinsonism
G214Vascular parkinsonism
G218Other secondary parkinsonism
G219Secondary parkinsonism, unspecified
 
PDX Collection 6826
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
G3180Leukodystrophy, unspecified
G3181Alpers disease
G3182Leigh's disease
G3184Mild cognitive impairment of uncertain or unknown etiology
G3185Corticobasal degeneration
G3186Alexander disease
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 6827
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
Q872Congenital malformation syndromes predominantly involving limbs
Q873Congenital malformation syndromes involving early overgrowth
Q8740Marfan syndrome, unspecified
Q87410Marfan syndrome with aortic dilation
Q87418Marfan syndrome with other cardiovascular manifestations
Q8742Marfan syndrome with ocular manifestations
Q8743Marfan syndrome with skeletal manifestation
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
Q898Other specified congenital malformations
Q992Fragile X chromosome
 
PDX Collection 6828
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
G3180Leukodystrophy, unspecified
G3181Alpers disease
G3182Leigh's disease
G3184Mild cognitive impairment of uncertain or unknown etiology
G3185Corticobasal degeneration
G3186Alexander disease
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 6829
D474Osteomyelofibrosis
D500Iron deficiency anemia secondary to blood loss (chronic)
D501Sideropenic dysphagia
D508Other iron deficiency anemias
D509Iron deficiency anemia, unspecified
D510Vitamin B12 deficiency anemia due to intrinsic factor deficiency
D511Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria
D512Transcobalamin II deficiency
D513Other dietary vitamin B12 deficiency anemia
D518Other vitamin B12 deficiency anemias
D519Vitamin B12 deficiency anemia, unspecified
D520Dietary folate deficiency anemia
D521Drug-induced folate deficiency anemia
D528Other folate deficiency anemias
D529Folate deficiency anemia, unspecified
D530Protein deficiency anemia
D531Other megaloblastic anemias, not elsewhere classified
D532Scorbutic anemia
D538Other specified nutritional anemias
D539Nutritional anemia, unspecified
D550Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
D551Anemia due to other disorders of glutathione metabolism
D553Anemia due to disorders of nucleotide metabolism
D558Other anemias due to enzyme disorders
D559Anemia due to enzyme disorder, unspecified
D560Alpha thalassemia
D561Beta thalassemia
D562Delta-beta thalassemia
D563Thalassemia minor
D564Hereditary persistence of fetal hemoglobin [HPFH]
D565Hemoglobin E-beta thalassemia
D568Other thalassemias
D569Thalassemia, unspecified
D5700Hb-SS disease with crisis, unspecified
D5701Hb-SS disease with acute chest syndrome
D5702Hb-SS disease with splenic sequestration
D5703Hb-SS disease with cerebral vascular involvement
D5704Hb-SS disease with dactylitis
D5709Hb-SS disease with crisis with other specified complication
D571Sickle-cell disease without crisis
D5720Sickle-cell/Hb-C disease without crisis
D57211Sickle-cell/Hb-C disease with acute chest syndrome
D57212Sickle-cell/Hb-C disease with splenic sequestration
D57219Sickle-cell/Hb-C disease with crisis, unspecified
D573Sickle-cell trait
D5740Sickle-cell thalassemia without crisis
D57411Sickle-cell thalassemia, unspecified, with acute chest syndrome
D57412Sickle-cell thalassemia, unspecified, with splenic sequestration
D57413Sickle-cell thalassemia, unspecified, with cerebral vascular involvement
D57414Sickle-cell thalassemia, unspecified, with dactylitis
D57418Sickle-cell thalassemia, unspecified, with crisis with other specified complication
D57419Sickle-cell thalassemia, unspecified, with crisis
D5742Sickle-cell thalassemia beta zero without crisis
D57431Sickle-cell thalassemia beta zero with acute chest syndrome
D57432Sickle-cell thalassemia beta zero with splenic sequestration
D57433Sickle-cell thalassemia beta zero with cerebral vascular involvement
D57434Sickle-cell thalassemia beta zero with dactylitis
D57438Sickle-cell thalassemia beta zero with crisis with other specified complication
D57439Sickle-cell thalassemia beta zero with crisis, unspecified
D5744Sickle-cell thalassemia beta plus without crisis
D57451Sickle-cell thalassemia beta plus with acute chest syndrome
D57452Sickle-cell thalassemia beta plus with splenic sequestration
D57453Sickle-cell thalassemia beta plus with cerebral vascular involvement
D57454Sickle-cell thalassemia beta plus with dactylitis
D57458Sickle-cell thalassemia beta plus with crisis with other specified complication
D57459Sickle-cell thalassemia beta plus with crisis, unspecified
D5780Other sickle-cell disorders without crisis
D57811Other sickle-cell disorders with acute chest syndrome
D57812Other sickle-cell disorders with splenic sequestration
D57813Other sickle-cell disorders with cerebral vascular involvement
D57814Other sickle-cell disorders with dactylitis
D57818Other sickle-cell disorders with crisis with other specified complication
D57819Other sickle-cell disorders with crisis, unspecified
D580Hereditary spherocytosis
D581Hereditary elliptocytosis
D582Other hemoglobinopathies
D588Other specified hereditary hemolytic anemias
D589Hereditary hemolytic anemia, unspecified
D590Drug-induced autoimmune hemolytic anemia
D592Drug-induced nonautoimmune hemolytic anemia
D5930Hemolytic-uremic syndrome, unspecified
D5931Infection-associated hemolytic-uremic syndrome
D5932Hereditary hemolytic-uremic syndrome
D5939Other hemolytic-uremic syndrome
D594Other nonautoimmune hemolytic anemias
D595Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]
D596Hemoglobinuria due to hemolysis from other external causes
D598Other acquired hemolytic anemias
D599Acquired hemolytic anemia, unspecified
D600Chronic acquired pure red cell aplasia
D601Transient acquired pure red cell aplasia
D608Other acquired pure red cell aplasias
D609Acquired pure red cell aplasia, unspecified
D6101Constitutional (pure) red blood cell aplasia
D6102Shwachman-Diamond syndrome
D6109Other constitutional aplastic anemia
D611Drug-induced aplastic anemia
D612Aplastic anemia due to other external agents
D613Idiopathic aplastic anemia
D61810Antineoplastic chemotherapy induced pancytopenia
D61811Other drug-induced pancytopenia
D61818Other pancytopenia
D6182Myelophthisis
D6189Other specified aplastic anemias and other bone marrow failure syndromes
D619Aplastic anemia, unspecified
D62Acute posthemorrhagic anemia



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