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 1214 of 1324
PDX Collection 6630 (continued)
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
G903Multi-system degeneration of the autonomic nervous system
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
G930Cerebral cysts
G931Anoxic brain damage, not elsewhere classified
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
G988Other disorders of nervous system
I6783Posterior reversible encephalopathy syndrome
R532Functional quadriplegia
 
PDX Collection 6631
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
 
PDX Collection 6632
G890Central pain syndrome
G8911Acute pain due to trauma
G8912Acute post-thoracotomy pain
G8918Other acute postprocedural pain
G8921Chronic pain due to trauma
G8922Chronic post-thoracotomy pain
G8928Other chronic postprocedural pain
G8929Other chronic pain
G893Neoplasm related pain (acute) (chronic)
G894Chronic pain syndrome
R0989Other specified symptoms and signs involving the circulatory and respiratory systems
R09A0Foreign body sensation, unspecified
R09A1Foreign body sensation, nose
R09A2Foreign body sensation, throat
R09A9Foreign body sensation, other site
R410Disorientation, unspecified
R411Anterograde amnesia
R412Retrograde amnesia
R413Other amnesia
R4182Altered mental status, unspecified
R419Unspecified symptoms and signs involving cognitive functions and awareness
R448Other symptoms and signs involving general sensations and perceptions
R449Unspecified symptoms and signs involving general sensations and perceptions
R4583Excessive crying of child, adolescent or adult
R4584Anhedonia
R460Very low level of personal hygiene
R461Bizarre personal appearance
R462Strange and inexplicable behavior
R463Overactivity
R464Slowness and poor responsiveness
R465Suspiciousness and marked evasiveness
R466Undue concern and preoccupation with stressful events
R467Verbosity and circumstantial detail obscuring reason for contact
R52Pain, unspecified
R570Cardiogenic shock
R571Hypovolemic shock
R578Other shock
R579Shock, unspecified
R680Hypothermia, not associated with low environmental temperature
R6811Excessive crying of infant (baby)
R6812Fussy infant (baby)
R6813Apparent life threatening event in infant (ALTE)
R6819Other nonspecific symptoms peculiar to infancy
R6881Early satiety
R6882Decreased libido
R6883Chills (without fever)
R6889Other general symptoms and signs
R69Illness, unspecified
 
PDX Collection 6633
G890Central pain syndrome
G8911Acute pain due to trauma
G8912Acute post-thoracotomy pain
G8918Other acute postprocedural pain
G8921Chronic pain due to trauma
G8922Chronic post-thoracotomy pain
G8928Other chronic postprocedural pain
G8929Other chronic pain
G893Neoplasm related pain (acute) (chronic)
G894Chronic pain syndrome
R0989Other specified symptoms and signs involving the circulatory and respiratory systems
R09A0Foreign body sensation, unspecified
R09A1Foreign body sensation, nose
R09A2Foreign body sensation, throat
R09A9Foreign body sensation, other site
R410Disorientation, unspecified
R411Anterograde amnesia
R412Retrograde amnesia
R413Other amnesia
R4182Altered mental status, unspecified
R419Unspecified symptoms and signs involving cognitive functions and awareness
R448Other symptoms and signs involving general sensations and perceptions
R449Unspecified symptoms and signs involving general sensations and perceptions
R4583Excessive crying of child, adolescent or adult
R4584Anhedonia
R460Very low level of personal hygiene
R461Bizarre personal appearance
R462Strange and inexplicable behavior
R463Overactivity
R464Slowness and poor responsiveness
R465Suspiciousness and marked evasiveness
R466Undue concern and preoccupation with stressful events
R467Verbosity and circumstantial detail obscuring reason for contact
R52Pain, unspecified
R570Cardiogenic shock
R571Hypovolemic shock
R578Other shock
R579Shock, unspecified
R680Hypothermia, not associated with low environmental temperature
R6811Excessive crying of infant (baby)
R6812Fussy infant (baby)
R6813Apparent life threatening event in infant (ALTE)
R6819Other nonspecific symptoms peculiar to infancy
R6881Early satiety
R6882Decreased libido
R6883Chills (without fever)
R6889Other general symptoms and signs
R69Illness, unspecified
 
PDX Collection 6634
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
P2930Pulmonary hypertension of newborn
P2938Other persistent fetal circulation
Q209Congenital malformation of cardiac chambers and connections, unspecified
Q238Other congenital malformations of aortic and mitral valves
Q239Congenital malformation of aortic and mitral valves, unspecified
Q242Cor triatriatum
Q243Pulmonary infundibular stenosis
Q244Congenital subaortic stenosis
Q248Other specified congenital malformations of heart
Q249Congenital malformation of heart, unspecified
Q2730Arteriovenous malformation, site unspecified
Q274Congenital phlebectasia
Q280Arteriovenous malformation of precerebral vessels
Q281Other malformations of precerebral vessels
Q288Other specified congenital malformations of circulatory system
Q289Congenital malformation of circulatory 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 6635
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
P2930Pulmonary hypertension of newborn
P2938Other persistent fetal circulation
Q209Congenital malformation of cardiac chambers and connections, unspecified
Q238Other congenital malformations of aortic and mitral valves
Q239Congenital malformation of aortic and mitral valves, unspecified
Q242Cor triatriatum
Q243Pulmonary infundibular stenosis
Q244Congenital subaortic stenosis
Q248Other specified congenital malformations of heart
Q249Congenital malformation of heart, unspecified
Q2730Arteriovenous malformation, site unspecified
Q274Congenital phlebectasia
Q280Arteriovenous malformation of precerebral vessels
Q281Other malformations of precerebral vessels
Q288Other specified congenital malformations of circulatory system
Q289Congenital malformation of circulatory 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 6636
A021Salmonella sepsis
A207Septicemic plague
A227Anthrax sepsis
A392Acute meningococcemia
A393Chronic meningococcemia
A394Meningococcemia, unspecified
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]
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
B007Disseminated herpesviral disease
B92Sequelae of leprosy
B942Sequelae of viral hepatitis
B948Sequelae of other specified infectious and parasitic diseases
B949Sequelae of unspecified infectious and parasitic disease
P392Intra-amniotic infection affecting newborn, not elsewhere classified
P393Neonatal urinary tract infection
P394Neonatal skin infection
P398Other specified infections specific to the perinatal period
P399Infection specific to the perinatal period, unspecified
P95Stillbirth
P969Condition originating in the perinatal period, unspecified
R7881Bacteremia
 
PDX Collection 6637
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
P2930Pulmonary hypertension of newborn
P2938Other persistent fetal circulation
Q209Congenital malformation of cardiac chambers and connections, unspecified
Q238Other congenital malformations of aortic and mitral valves
Q239Congenital malformation of aortic and mitral valves, unspecified
Q246Congenital heart block
Q248Other specified congenital malformations of heart
Q249Congenital malformation of heart, unspecified
Q2730Arteriovenous malformation, site unspecified
Q274Congenital phlebectasia
Q280Arteriovenous malformation of precerebral vessels
Q281Other malformations of precerebral vessels
Q288Other specified congenital malformations of circulatory system
Q289Congenital malformation of circulatory 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 6638
A021Salmonella sepsis
A207Septicemic plague
A227Anthrax sepsis
A392Acute meningococcemia
A393Chronic meningococcemia
A394Meningococcemia, unspecified
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]
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
B007Disseminated herpesviral disease
B92Sequelae of leprosy
B942Sequelae of viral hepatitis
B948Sequelae of other specified infectious and parasitic diseases
B949Sequelae of unspecified infectious and parasitic disease
P392Intra-amniotic infection affecting newborn, not elsewhere classified
P393Neonatal urinary tract infection
P394Neonatal skin infection
P398Other specified infections specific to the perinatal period
P399Infection specific to the perinatal period, unspecified
P95Stillbirth
P969Condition originating in the perinatal period, unspecified
R7881Bacteremia
 
PDX Collection 6639
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
Q251Coarctation of aorta
Q2521Interruption of aortic arch
Q2529Other atresia of aorta
Q253Supravalvular aortic stenosis
Q2730Arteriovenous malformation, site unspecified
Q274Congenital phlebectasia
Q280Arteriovenous malformation of precerebral vessels
Q281Other malformations of precerebral vessels
Q288Other specified congenital malformations of circulatory system
Q289Congenital malformation of circulatory system, unspecified
Q872Congenital malformation syndromes predominantly involving limbs
Q873Congenital malformation syndromes involving early overgrowth
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
 
PDX Collection 6640
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
P2930Pulmonary hypertension of newborn
P2938Other persistent fetal circulation
Q251Coarctation of aorta
Q2521Interruption of aortic arch
Q2529Other atresia of aorta
Q253Supravalvular aortic stenosis
Q2730Arteriovenous malformation, site unspecified
Q274Congenital phlebectasia
Q280Arteriovenous malformation of precerebral vessels
Q281Other malformations of precerebral vessels
Q288Other specified congenital malformations of circulatory system
Q289Congenital malformation of circulatory system, unspecified
Q8711Prader-Willi syndrome



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