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 1272 of 1375
PDX Collection 6682 (continued)
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
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 6683
A021Salmonella sepsis
A207Septicemic plague
A227Anthrax sepsis
A267Erysipelothrix sepsis
A327Listerial sepsis
A392Acute meningococcemia
A393Chronic meningococcemia
A394Meningococcemia, unspecified
A400Sepsis due to streptococcus, group A
A401Sepsis due to streptococcus, group B
A408Other streptococcal sepsis
A409Streptococcal sepsis, unspecified
A4101Sepsis due to Methicillin susceptible Staphylococcus aureus
A4102Sepsis due to Methicillin resistant Staphylococcus aureus
A411Sepsis due to other specified staphylococcus
A412Sepsis due to unspecified staphylococcus
A413Sepsis due to Hemophilus influenzae
A414Sepsis due to anaerobes
A4150Gram-negative sepsis, unspecified
A4151Sepsis due to Escherichia coli [E. coli]
A4152Sepsis due to Pseudomonas
A4153Sepsis due to Serratia
A4154Sepsis due to Acinetobacter baumannii
A4159Other Gram-negative sepsis
A4181Sepsis due to Enterococcus
A4189Other specified sepsis
A419Sepsis, unspecified organism
A427Actinomycotic sepsis
A482Nonpneumonic Legionnaires' disease [Pontiac fever]
A483Toxic shock syndrome
A484Brazilian purpuric fever
A488Other specified bacterial diseases
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
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 6684
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
G901Familial dysautonomia [Riley-Day]
Q050Cervical spina bifida with hydrocephalus
Q051Thoracic spina bifida with hydrocephalus
Q052Lumbar spina bifida with hydrocephalus
Q053Sacral spina bifida with hydrocephalus
Q054Unspecified spina bifida with hydrocephalus
Q055Cervical spina bifida without hydrocephalus
Q056Thoracic spina bifida without hydrocephalus
Q057Lumbar spina bifida without hydrocephalus
Q058Sacral spina bifida without hydrocephalus
Q059Spina bifida, unspecified
Q060Amyelia
Q061Hypoplasia and dysplasia of spinal cord
Q063Other congenital cauda equina malformations
Q068Other specified congenital malformations of spinal cord
Q069Congenital malformation of spinal cord, unspecified
Q0700Arnold-Chiari syndrome without spina bifida or hydrocephalus
Q0701Arnold-Chiari syndrome with spina bifida
Q0702Arnold-Chiari syndrome with hydrocephalus
Q0703Arnold-Chiari syndrome with spina bifida and hydrocephalus
Q078Other specified congenital malformations of nervous system
Q079Congenital malformation of nervous system, unspecified
Q8711Prader-Willi syndrome
Q8719Other congenital malformation syndromes predominantly associated with short stature
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
Q897Multiple congenital malformations, not elsewhere classified
Q898Other specified congenital malformations
Q992Fragile X chromosome
 
PDX Collection 6685
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
G901Familial dysautonomia [Riley-Day]
Q050Cervical spina bifida with hydrocephalus
Q051Thoracic spina bifida with hydrocephalus
Q052Lumbar spina bifida with hydrocephalus
Q053Sacral spina bifida with hydrocephalus
Q054Unspecified spina bifida with hydrocephalus
Q055Cervical spina bifida without hydrocephalus
Q056Thoracic spina bifida without hydrocephalus
Q057Lumbar spina bifida without hydrocephalus
Q058Sacral spina bifida without hydrocephalus
Q059Spina bifida, unspecified
Q060Amyelia
Q061Hypoplasia and dysplasia of spinal cord
Q063Other congenital cauda equina malformations
Q068Other specified congenital malformations of spinal cord
Q069Congenital malformation of spinal cord, unspecified
Q0700Arnold-Chiari syndrome without spina bifida or hydrocephalus
Q0701Arnold-Chiari syndrome with spina bifida
Q0702Arnold-Chiari syndrome with hydrocephalus
Q0703Arnold-Chiari syndrome with spina bifida and hydrocephalus
Q078Other specified congenital malformations of nervous system
Q079Congenital malformation of nervous system, unspecified
Q8711Prader-Willi syndrome
Q8719Other congenital malformation syndromes predominantly associated with short stature
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
Q897Multiple congenital malformations, not elsewhere classified
Q898Other specified congenital malformations
Q992Fragile X chromosome
 
PDX Collection 6686
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
G901Familial dysautonomia [Riley-Day]
Q050Cervical spina bifida with hydrocephalus
Q051Thoracic spina bifida with hydrocephalus
Q052Lumbar spina bifida with hydrocephalus
Q053Sacral spina bifida with hydrocephalus
Q054Unspecified spina bifida with hydrocephalus
Q055Cervical spina bifida without hydrocephalus
Q056Thoracic spina bifida without hydrocephalus
Q057Lumbar spina bifida without hydrocephalus
Q058Sacral spina bifida without hydrocephalus
Q059Spina bifida, unspecified
Q060Amyelia
Q061Hypoplasia and dysplasia of spinal cord
Q063Other congenital cauda equina malformations
Q068Other specified congenital malformations of spinal cord
Q069Congenital malformation of spinal cord, unspecified
Q0700Arnold-Chiari syndrome without spina bifida or hydrocephalus
Q0701Arnold-Chiari syndrome with spina bifida
Q0702Arnold-Chiari syndrome with hydrocephalus
Q0703Arnold-Chiari syndrome with spina bifida and hydrocephalus
Q078Other specified congenital malformations of nervous system
Q079Congenital malformation of nervous system, unspecified
Q8711Prader-Willi syndrome
Q8719Other congenital malformation syndromes predominantly associated with short stature
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
Q897Multiple congenital malformations, not elsewhere classified
Q898Other specified congenital malformations
Q992Fragile X chromosome
 
PDX Collection 6687
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
G901Familial dysautonomia [Riley-Day]
Q050Cervical spina bifida with hydrocephalus
Q051Thoracic spina bifida with hydrocephalus
Q052Lumbar spina bifida with hydrocephalus
Q053Sacral spina bifida with hydrocephalus
Q054Unspecified spina bifida with hydrocephalus
Q055Cervical spina bifida without hydrocephalus
Q056Thoracic spina bifida without hydrocephalus
Q057Lumbar spina bifida without hydrocephalus
Q058Sacral spina bifida without hydrocephalus
Q059Spina bifida, unspecified
Q060Amyelia
Q061Hypoplasia and dysplasia of spinal cord
Q063Other congenital cauda equina malformations
Q068Other specified congenital malformations of spinal cord
Q069Congenital malformation of spinal cord, unspecified
Q0700Arnold-Chiari syndrome without spina bifida or hydrocephalus
Q0701Arnold-Chiari syndrome with spina bifida
Q0702Arnold-Chiari syndrome with hydrocephalus
Q0703Arnold-Chiari syndrome with spina bifida and hydrocephalus
Q078Other specified congenital malformations of nervous system
Q079Congenital malformation of nervous system, unspecified
Q8711Prader-Willi syndrome
Q8719Other congenital malformation syndromes predominantly associated with short stature
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
Q897Multiple congenital malformations, not elsewhere classified
Q898Other specified congenital malformations
Q992Fragile X chromosome
 
PDX Collection 6688
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
G901Familial dysautonomia [Riley-Day]
Q050Cervical spina bifida with hydrocephalus
Q051Thoracic spina bifida with hydrocephalus
Q052Lumbar spina bifida with hydrocephalus
Q053Sacral spina bifida with hydrocephalus
Q054Unspecified spina bifida with hydrocephalus
Q055Cervical spina bifida without hydrocephalus
Q056Thoracic spina bifida without hydrocephalus
Q057Lumbar spina bifida without hydrocephalus
Q058Sacral spina bifida without hydrocephalus
Q059Spina bifida, unspecified
Q060Amyelia
Q061Hypoplasia and dysplasia of spinal cord
Q063Other congenital cauda equina malformations
Q068Other specified congenital malformations of spinal cord
Q069Congenital malformation of spinal cord, unspecified
Q0700Arnold-Chiari syndrome without spina bifida or hydrocephalus
Q0701Arnold-Chiari syndrome with spina bifida
Q0702Arnold-Chiari syndrome with hydrocephalus
Q0703Arnold-Chiari syndrome with spina bifida and hydrocephalus
Q078Other specified congenital malformations of nervous system
Q079Congenital malformation of nervous system, unspecified
Q8711Prader-Willi syndrome
Q8719Other congenital malformation syndromes predominantly associated with short stature
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
Q897Multiple congenital malformations, not elsewhere classified
Q898Other specified congenital malformations
Q992Fragile X chromosome
 
PDX Collection 6689
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 6690
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



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01 Mar 2023 06:12:40
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