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 1251 of 1375
PDX Collection 6595 (continued)
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
R4681Obsessive-compulsive behavior
R4689Other symptoms and signs involving appearance and behavior
R52Pain, unspecified
R570Cardiogenic shock
R571Hypovolemic shock
R578Other shock
R579Shock, unspecified
R6521Severe sepsis with septic shock
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 6596
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
P2930Pulmonary hypertension of newborn
P2938Other persistent fetal circulation
Q209Congenital malformation of cardiac chambers and connections, unspecified
Q224Congenital tricuspid stenosis
Q225Ebstein's anomaly
Q226Hypoplastic right heart syndrome
Q228Other congenital malformations of tricuspid valve
Q229Congenital malformation of tricuspid valve, unspecified
Q230Congenital stenosis of aortic valve
Q231Congenital insufficiency of aortic valve
Q232Congenital mitral stenosis
Q233Congenital mitral insufficiency
Q234Hypoplastic left heart syndrome
Q238Other congenital malformations of aortic and mitral valves
Q239Congenital malformation of aortic and mitral valves, unspecified
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 6597
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
P2930Pulmonary hypertension of newborn
P2938Other persistent fetal circulation
Q209Congenital malformation of cardiac chambers and connections, unspecified
Q224Congenital tricuspid stenosis
Q225Ebstein's anomaly
Q226Hypoplastic right heart syndrome
Q228Other congenital malformations of tricuspid valve
Q229Congenital malformation of tricuspid valve, unspecified
Q230Congenital stenosis of aortic valve
Q231Congenital insufficiency of aortic valve
Q232Congenital mitral stenosis
Q233Congenital mitral insufficiency
Q234Hypoplastic left heart syndrome
Q238Other congenital malformations of aortic and mitral valves
Q239Congenital malformation of aortic and mitral valves, unspecified
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 6598
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
P2930Pulmonary hypertension of newborn
P2938Other persistent fetal circulation
Q209Congenital malformation of cardiac chambers and connections, unspecified
Q224Congenital tricuspid stenosis
Q225Ebstein's anomaly
Q226Hypoplastic right heart syndrome
Q228Other congenital malformations of tricuspid valve
Q229Congenital malformation of tricuspid valve, unspecified
Q230Congenital stenosis of aortic valve
Q231Congenital insufficiency of aortic valve
Q232Congenital mitral stenosis
Q233Congenital mitral insufficiency
Q234Hypoplastic left heart syndrome
Q238Other congenital malformations of aortic and mitral valves
Q239Congenital malformation of aortic and mitral valves, unspecified
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 6599
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
Q209Congenital malformation of cardiac chambers and connections, unspecified
Q220Pulmonary valve atresia
Q221Congenital pulmonary valve stenosis
Q222Congenital pulmonary valve insufficiency
Q223Other congenital malformations of pulmonary valve
Q238Other congenital malformations of aortic and mitral valves
Q239Congenital malformation of aortic and mitral valves, unspecified
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
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 6600
E0840Diabetes mellitus due to underlying condition with diabetic neuropathy, unspecified
E0841Diabetes mellitus due to underlying condition with diabetic mononeuropathy
E0842Diabetes mellitus due to underlying condition with diabetic polyneuropathy
E0843Diabetes mellitus due to underlying condition with diabetic autonomic (poly)neuropathy
E0844Diabetes mellitus due to underlying condition with diabetic amyotrophy
E0849Diabetes mellitus due to underlying condition with other diabetic neurological complication
E0940Drug or chemical induced diabetes mellitus with neurological complications with diabetic neuropathy, unspecified
E0941Drug or chemical induced diabetes mellitus with neurological complications with diabetic mononeuropathy
E0942Drug or chemical induced diabetes mellitus with neurological complications with diabetic polyneuropathy
E0943Drug or chemical induced diabetes mellitus with neurological complications with diabetic autonomic (poly)neuropathy
E0944Drug or chemical induced diabetes mellitus with neurological complications with diabetic amyotrophy
E0949Drug or chemical induced diabetes mellitus with neurological complications with other diabetic neurological complication
E1040Type 1 diabetes mellitus with diabetic neuropathy, unspecified
E1041Type 1 diabetes mellitus with diabetic mononeuropathy
E1042Type 1 diabetes mellitus with diabetic polyneuropathy
E1043Type 1 diabetes mellitus with diabetic autonomic (poly)neuropathy
E1044Type 1 diabetes mellitus with diabetic amyotrophy
E1049Type 1 diabetes mellitus with other diabetic neurological complication
E1140Type 2 diabetes mellitus with diabetic neuropathy, unspecified
E1141Type 2 diabetes mellitus with diabetic mononeuropathy
E1142Type 2 diabetes mellitus with diabetic polyneuropathy
E1143Type 2 diabetes mellitus with diabetic autonomic (poly)neuropathy
E1144Type 2 diabetes mellitus with diabetic amyotrophy
E1149Type 2 diabetes mellitus with other diabetic neurological complication
E1340Other specified diabetes mellitus with diabetic neuropathy, unspecified
E1341Other specified diabetes mellitus with diabetic mononeuropathy
E1342Other specified diabetes mellitus with diabetic polyneuropathy
E1343Other specified diabetes mellitus with diabetic autonomic (poly)neuropathy
E1344Other specified diabetes mellitus with diabetic amyotrophy
E1349Other specified diabetes mellitus with other diabetic neurological complication
G3289Other specified degenerative disorders of nervous system in diseases classified elsewhere
G40001Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, with status epilepticus
G40009Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, without status epilepticus
G40011Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, with status epilepticus
G40019Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, without status epilepticus
G40101Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, with status epilepticus
G40109Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, without status epilepticus
G40111Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, with status epilepticus
G40119Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, without status epilepticus
G40201Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, with status epilepticus
G40209Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, without status epilepticus
G40211Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, with status epilepticus
G40219Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, without status epilepticus
G40301Generalized idiopathic epilepsy and epileptic syndromes, not intractable, with status epilepticus
G40309Generalized idiopathic epilepsy and epileptic syndromes, not intractable, without status epilepticus
G40311Generalized idiopathic epilepsy and epileptic syndromes, intractable, with status epilepticus
G40319Generalized idiopathic epilepsy and epileptic syndromes, intractable, without status epilepticus
G40401Other generalized epilepsy and epileptic syndromes, not intractable, with status epilepticus
G40409Other generalized epilepsy and epileptic syndromes, not intractable, without status epilepticus
G40411Other generalized epilepsy and epileptic syndromes, intractable, with status epilepticus
G40419Other generalized epilepsy and epileptic syndromes, intractable, without status epilepticus
G4042Cyclin-Dependent Kinase-Like 5 Deficiency Disorder
G40501Epileptic seizures related to external causes, not intractable, with status epilepticus
G40509Epileptic seizures related to external causes, not intractable, without status epilepticus
G40801Other epilepsy, not intractable, with status epilepticus
G40802Other epilepsy, not intractable, without status epilepticus
G40803Other epilepsy, intractable, with status epilepticus
G40804Other epilepsy, intractable, without status epilepticus
G40811Lennox-Gastaut syndrome, not intractable, with status epilepticus
G40812Lennox-Gastaut syndrome, not intractable, without status epilepticus
G40813Lennox-Gastaut syndrome, intractable, with status epilepticus
G40814Lennox-Gastaut syndrome, intractable, without status epilepticus
G40821Epileptic spasms, not intractable, with status epilepticus
G40822Epileptic spasms, not intractable, without status epilepticus
G40823Epileptic spasms, intractable, with status epilepticus
G40824Epileptic spasms, intractable, without status epilepticus
G40833Dravet syndrome, intractable, with status epilepticus
G40834Dravet syndrome, intractable, without status epilepticus
G4089Other seizures
G40901Epilepsy, unspecified, not intractable, with status epilepticus
G40909Epilepsy, unspecified, not intractable, without status epilepticus
G40911Epilepsy, unspecified, intractable, with status epilepticus
G40919Epilepsy, unspecified, intractable, without status epilepticus
G40A01Absence epileptic syndrome, not intractable, with status epilepticus
G40A09Absence epileptic syndrome, not intractable, without status epilepticus
G40A11Absence epileptic syndrome, intractable, with status epilepticus
G40A19Absence epileptic syndrome, intractable, without status epilepticus
G40B01Juvenile myoclonic epilepsy, not intractable, with status epilepticus
G40B09Juvenile myoclonic epilepsy, not intractable, without status epilepticus
G40B11Juvenile myoclonic epilepsy, intractable, with status epilepticus
G40B19Juvenile myoclonic epilepsy, intractable, without status epilepticus
G40C01Lafora progressive myoclonus epilepsy, not intractable, with status epilepticus
G40C09Lafora progressive myoclonus epilepsy, not intractable, without status epilepticus
G40C11Lafora progressive myoclonus epilepsy, intractable, with status epilepticus
G40C19Lafora progressive myoclonus epilepsy, intractable, without status epilepticus
G9381Temporal sclerosis
G9389Other specified disorders of brain
G939Disorder of brain, unspecified
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
R561Post traumatic seizures
 
PDX Collection 6601
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
P2930Pulmonary hypertension of newborn
P2938Other persistent fetal circulation
Q209Congenital malformation of cardiac chambers and connections, unspecified
Q220Pulmonary valve atresia
Q221Congenital pulmonary valve stenosis
Q222Congenital pulmonary valve insufficiency
Q223Other congenital malformations of pulmonary valve
Q238Other congenital malformations of aortic and mitral valves
Q239Congenital malformation of aortic and mitral valves, unspecified
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 6602
K3189Other diseases of stomach and duodenum
K319Disease of stomach and duodenum, unspecified
K35200Acute appendicitis with generalized peritonitis, without perforation or abscess
K35201Acute appendicitis with generalized peritonitis, with perforation, without abscess
K35209Acute appendicitis with generalized peritonitis, without abscess, unspecified as to perforation
K35210Acute appendicitis with generalized peritonitis, without perforation, with abscess
K35211Acute appendicitis with generalized peritonitis, with perforation and abscess
K35219Acute appendicitis with generalized peritonitis, with abscess, unspecified as to perforation
K3530Acute appendicitis with localized peritonitis, without perforation or gangrene
K3531Acute appendicitis with localized peritonitis and gangrene, without perforation
K3532Acute appendicitis with perforation, localized peritonitis, and gangrene, without abscess
K3533Acute appendicitis with perforation, localized peritonitis, and gangrene, with abscess
K3580Unspecified acute appendicitis
K35890Other acute appendicitis without perforation or gangrene
K35891Other acute appendicitis without perforation, with gangrene
K36Other appendicitis
K37Unspecified appendicitis
K380Hyperplasia of appendix
K381Appendicular concretions
K382Diverticulum of appendix
K383Fistula of appendix
K388Other specified diseases of appendix
K389Disease of appendix, unspecified
K9281Gastrointestinal mucositis (ulcerative)
 
PDX Collection 6603
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
P2930Pulmonary hypertension of newborn
P2938Other persistent fetal circulation
Q209Congenital malformation of cardiac chambers and connections, unspecified
Q224Congenital tricuspid stenosis
Q225Ebstein's anomaly
Q226Hypoplastic right heart syndrome
Q228Other congenital malformations of tricuspid valve
Q229Congenital malformation of tricuspid valve, unspecified
Q230Congenital stenosis of aortic valve
Q231Congenital insufficiency of aortic valve
Q232Congenital mitral stenosis
Q233Congenital mitral insufficiency
Q234Hypoplastic left heart syndrome
Q238Other congenital malformations of aortic and mitral valves
Q239Congenital malformation of aortic and mitral valves, unspecified
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 6604
K3189Other diseases of stomach and duodenum
K319Disease of stomach and duodenum, unspecified
K35200Acute appendicitis with generalized peritonitis, without perforation or abscess
K35201Acute appendicitis with generalized peritonitis, with perforation, without abscess
K35209Acute appendicitis with generalized peritonitis, without abscess, unspecified as to perforation
K35210Acute appendicitis with generalized peritonitis, without perforation, with abscess



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