ICD-10-CM/PCS MS-DRG v41.1 Definitions Manual

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Appendix C: Principal diagnoses which convert CC/MCC to non-CC
Page 305 of 429
 
PDX Collection 1508
P760Meconium plug syndrome
P761Transitory ileus of newborn
P762Intestinal obstruction due to inspissated milk
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
P780Perinatal intestinal perforation
P781Other neonatal peritonitis
P782Neonatal hematemesis and melena due to swallowed maternal blood
P783Noninfective neonatal diarrhea
P7881Congenital cirrhosis (of liver)
P7882Peptic ulcer of newborn
P7883Newborn esophageal reflux
P7884Gestational alloimmune liver disease
P7889Other specified perinatal digestive system disorders
P789Perinatal digestive system disorder, unspecified
 
PDX Collection 1509
P290Neonatal cardiac failure
P2911Neonatal tachycardia
P2912Neonatal bradycardia
P292Neonatal hypertension
P294Transient myocardial ischemia in newborn
P2989Other cardiovascular disorders originating in the perinatal period
P299Cardiovascular disorder originating in the perinatal period, unspecified
P760Meconium plug syndrome
P761Transitory ileus of newborn
P762Intestinal obstruction due to inspissated milk
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
P780Perinatal intestinal perforation
P781Other neonatal peritonitis
P782Neonatal hematemesis and melena due to swallowed maternal blood
P783Noninfective neonatal diarrhea
P7881Congenital cirrhosis (of liver)
P7882Peptic ulcer of newborn
P7883Newborn esophageal reflux
P7884Gestational alloimmune liver disease
P7889Other specified perinatal digestive system disorders
P789Perinatal digestive system disorder, unspecified
P941Congenital hypertonia
P942Congenital hypotonia
P948Other disorders of muscle tone of newborn
P949Disorder of muscle tone of newborn, unspecified
P960Congenital renal failure
P963Wide cranial sutures of newborn
P965Complication to newborn due to (fetal) intrauterine procedure
P9682Delayed separation of umbilical cord
P9683Meconium staining
P9689Other specified conditions originating in the perinatal period
 
PDX Collection 1510
P830Sclerema neonatorum
P8330Unspecified edema specific to newborn
P8339Other edema specific to newborn
 
PDX Collection 1511
P290Neonatal cardiac failure
P2911Neonatal tachycardia
P2912Neonatal bradycardia
P292Neonatal hypertension
P294Transient myocardial ischemia in newborn
P2989Other cardiovascular disorders originating in the perinatal period
P299Cardiovascular disorder originating in the perinatal period, unspecified
P832Hydrops fetalis not due to hemolytic disease
P941Congenital hypertonia
P942Congenital hypotonia
P948Other disorders of muscle tone of newborn
P949Disorder of muscle tone of newborn, unspecified
P960Congenital renal failure
P963Wide cranial sutures of newborn
P965Complication to newborn due to (fetal) intrauterine procedure
P9682Delayed separation of umbilical cord
P9683Meconium staining
P9689Other specified conditions originating in the perinatal period
 
PDX Collection 1512
P800Cold injury syndrome
P808Other hypothermia of newborn
P809Hypothermia of newborn, unspecified
P810Environmental hyperthermia of newborn
P818Other specified disturbances of temperature regulation of newborn
P819Disturbance of temperature regulation of newborn, unspecified
P830Sclerema neonatorum
P8330Unspecified edema specific to newborn
P8339Other edema specific to newborn
 
PDX Collection 1513
P290Neonatal cardiac failure
P2911Neonatal tachycardia
P2912Neonatal bradycardia
P292Neonatal hypertension
P294Transient myocardial ischemia in newborn
P2989Other cardiovascular disorders originating in the perinatal period
P299Cardiovascular disorder originating in the perinatal period, unspecified
P90Convulsions of newborn
P91819Neonatal encephalopathy, unspecified
P91821Neonatal cerebral infarction, right side of brain
P91822Neonatal cerebral infarction, left side of brain
P91823Neonatal cerebral infarction, bilateral
P91829Neonatal cerebral infarction, unspecified side
P9188Other specified disturbances of cerebral status of newborn
P919Disturbance of cerebral status of newborn, unspecified
P941Congenital hypertonia
P942Congenital hypotonia
P948Other disorders of muscle tone of newborn
P949Disorder of muscle tone of newborn, unspecified
P960Congenital renal failure
P963Wide cranial sutures of newborn
P965Complication to newborn due to (fetal) intrauterine procedure
P9682Delayed separation of umbilical cord
P9683Meconium staining
P9689Other specified conditions originating in the perinatal period
 
PDX Collection 1514
P90Convulsions of newborn
P910Neonatal cerebral ischemia
P911Acquired periventricular cysts of newborn
P913Neonatal cerebral irritability
P914Neonatal cerebral depression
P915Neonatal coma
P91819Neonatal encephalopathy, unspecified
P91821Neonatal cerebral infarction, right side of brain
P91822Neonatal cerebral infarction, left side of brain
P91823Neonatal cerebral infarction, bilateral
P91829Neonatal cerebral infarction, unspecified side
P9188Other specified disturbances of cerebral status of newborn
P919Disturbance of cerebral status of newborn, unspecified
 
PDX Collection 1515
P84Other problems with newborn
P9160Hypoxic ischemic encephalopathy [HIE], unspecified
P9161Mild hypoxic ischemic encephalopathy [HIE]
P9162Moderate hypoxic ischemic encephalopathy [HIE]
P9163Severe hypoxic ischemic encephalopathy [HIE]
 
PDX Collection 1516
P91821Neonatal cerebral infarction, right side of brain
P91822Neonatal cerebral infarction, left side of brain
P91823Neonatal cerebral infarction, bilateral
P91829Neonatal cerebral infarction, unspecified side
 
PDX Collection 1517
P9201Bilious vomiting of newborn
P9209Other vomiting of newborn
 
PDX Collection 1518
P930Grey baby syndrome
P938Other reactions and intoxications due to drugs administered to newborn
P961Neonatal withdrawal symptoms from maternal use of drugs of addiction
P962Withdrawal symptoms from therapeutic use of drugs in newborn
 
PDX Collection 1519
Q000Anencephaly
Q001Craniorachischisis
Q002Iniencephaly
 
PDX Collection 1520
Q010Frontal encephalocele
Q011Nasofrontal encephalocele
Q012Occipital encephalocele
Q018Encephalocele of other sites
Q019Encephalocele, unspecified
Q02Microcephaly
Q040Congenital malformations of corpus callosum
Q041Arhinencephaly
Q042Holoprosencephaly
Q043Other reduction deformities of brain
Q044Septo-optic dysplasia of brain
Q045Megalencephaly
Q046Congenital cerebral cysts
Q048Other specified congenital malformations of brain
 
PDX Collection 1521
Q044Septo-optic dysplasia of brain
Q045Megalencephaly
Q046Congenital cerebral cysts
Q048Other specified congenital malformations of brain
 
PDX Collection 1522
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 1523
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
I230Hemopericardium as current complication following acute myocardial infarction
I231Atrial septal defect as current complication following acute myocardial infarction
I232Ventricular septal defect as current complication following acute myocardial infarction
I233Rupture of cardiac wall without hemopericardium as current complication following acute myocardial infarction
I236Thrombosis of atrium, auricular appendage, and ventricle as current complications following acute myocardial infarction
I237Postinfarction angina
I238Other current complications following acute myocardial infarction
I510Cardiac septal defect, acquired
P2930Pulmonary hypertension of newborn
P2938Other persistent fetal circulation
Q200Common arterial trunk
Q201Double outlet right ventricle
Q202Double outlet left ventricle
Q203Discordant ventriculoarterial connection
Q204Double inlet ventricle
Q205Discordant atrioventricular connection
Q206Isomerism of atrial appendages
Q208Other congenital malformations of cardiac chambers and connections
Q209Congenital malformation of cardiac chambers and connections, unspecified
Q210Ventricular septal defect
Q2110Atrial septal defect, unspecified
Q2111Secundum atrial septal defect
Q2112Patent foramen ovale
Q2113Coronary sinus atrial septal defect
Q2114Superior sinus venosus atrial septal defect
Q2115Inferior sinus venosus atrial septal defect
Q2116Sinus venosus atrial septal defect, unspecified
Q2119Other specified atrial septal defect
Q2120Atrioventricular septal defect, unspecified as to partial or complete
Q2121Partial atrioventricular septal defect
Q2122Transitional atrioventricular septal defect
Q2123Complete atrioventricular septal defect
Q213Tetralogy of Fallot
Q214Aortopulmonary septal defect
Q218Other congenital malformations of cardiac septa
Q219Congenital malformation of cardiac septum, unspecified
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 1524
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
I230Hemopericardium as current complication following acute myocardial infarction
I231Atrial septal defect as current complication following acute myocardial infarction
I232Ventricular septal defect as current complication following acute myocardial infarction
I233Rupture of cardiac wall without hemopericardium as current complication following acute myocardial infarction
I236Thrombosis of atrium, auricular appendage, and ventricle as current complications following acute myocardial infarction
I237Postinfarction angina
I238Other current complications following acute myocardial infarction
I510Cardiac septal defect, acquired
P2930Pulmonary hypertension of newborn
P2938Other persistent fetal circulation
Q200Common arterial trunk
Q201Double outlet right ventricle
Q202Double outlet left ventricle
Q203Discordant ventriculoarterial connection
Q204Double inlet ventricle
Q205Discordant atrioventricular connection
Q206Isomerism of atrial appendages
Q208Other congenital malformations of cardiac chambers and connections
Q209Congenital malformation of cardiac chambers and connections, unspecified
Q210Ventricular septal defect
Q2110Atrial septal defect, unspecified
Q2111Secundum atrial septal defect
Q2112Patent foramen ovale
Q2113Coronary sinus atrial septal defect
Q2114Superior sinus venosus atrial septal defect
Q2115Inferior sinus venosus atrial septal defect
Q2116Sinus venosus atrial septal defect, unspecified
Q2119Other specified atrial septal defect
Q2120Atrioventricular septal defect, unspecified as to partial or complete
Q2121Partial atrioventricular septal defect
Q2122Transitional atrioventricular septal defect
Q2123Complete atrioventricular septal defect
Q213Tetralogy of Fallot
Q214Aortopulmonary septal defect
Q218Other congenital malformations of cardiac septa
Q219Congenital malformation of cardiac septum, unspecified
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
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 1525
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
I230Hemopericardium as current complication following acute myocardial infarction
I231Atrial septal defect as current complication following acute myocardial infarction
I232Ventricular septal defect as current complication following acute myocardial infarction
I233Rupture of cardiac wall without hemopericardium as current complication following acute myocardial infarction
I236Thrombosis of atrium, auricular appendage, and ventricle as current complications following acute myocardial infarction
I237Postinfarction angina
I238Other current complications following acute myocardial infarction
I510Cardiac septal defect, acquired
Q200Common arterial trunk
Q201Double outlet right ventricle
Q202Double outlet left ventricle
Q203Discordant ventriculoarterial connection
Q204Double inlet ventricle
Q205Discordant atrioventricular connection
Q206Isomerism of atrial appendages
Q208Other congenital malformations of cardiac chambers and connections
Q209Congenital malformation of cardiac chambers and connections, unspecified
Q2110Atrial septal defect, unspecified
Q2111Secundum atrial septal defect
Q2112Patent foramen ovale
Q2113Coronary sinus atrial septal defect
Q2114Superior sinus venosus atrial septal defect
Q2115Inferior sinus venosus atrial septal defect
Q2116Sinus venosus atrial septal defect, unspecified
Q2119Other specified atrial septal defect
Q2120Atrioventricular septal defect, unspecified as to partial or complete
Q2121Partial atrioventricular septal defect
Q2122Transitional atrioventricular septal defect
Q2123Complete atrioventricular septal defect
Q213Tetralogy of Fallot
Q214Aortopulmonary septal defect
Q218Other congenital malformations of cardiac septa
Q219Congenital malformation of cardiac septum, unspecified
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
Q8781Alport syndrome
Q8782Arterial tortuosity syndrome
 
PDX Collection 1526
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
I230Hemopericardium as current complication following acute myocardial infarction
I231Atrial septal defect as current complication following acute myocardial infarction
I232Ventricular septal defect as current complication following acute myocardial infarction
I233Rupture of cardiac wall without hemopericardium as current complication following acute myocardial infarction
I236Thrombosis of atrium, auricular appendage, and ventricle as current complications following acute myocardial infarction
I237Postinfarction angina
I238Other current complications following acute myocardial infarction
I510Cardiac septal defect, acquired
P2930Pulmonary hypertension of newborn
P2938Other persistent fetal circulation
Q200Common arterial trunk
Q201Double outlet right ventricle
Q202Double outlet left ventricle
Q203Discordant ventriculoarterial connection
Q204Double inlet ventricle



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