ICD-10-CM/PCS MS-DRG v39.1 Definitions Manual

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Appendix C: Principal diagnoses which convert CC/MCC to non-CC
Page 320 of 689
PDX Collection 3462 (continued)
P7449Other transitory electrolyte disturbance of newborn
P745Transitory tyrosinemia of newborn
P749Transitory metabolic disturbance of newborn, unspecified
P940Transient neonatal myasthenia gravis
 
PDX Collection 3463
P700Syndrome of infant of mother with gestational diabetes
P701Syndrome of infant of a diabetic mother
P702Neonatal diabetes mellitus
P703Iatrogenic neonatal hypoglycemia
P704Other neonatal hypoglycemia
P709Transitory disorder of carbohydrate metabolism of newborn, unspecified
P710Cow's milk hypocalcemia in newborn
P711Other neonatal hypocalcemia
P712Neonatal hypomagnesemia
P713Neonatal tetany without calcium or magnesium deficiency
P714Transitory neonatal hypoparathyroidism
P718Other transitory neonatal disorders of calcium and magnesium metabolism
P719Transitory neonatal disorder of calcium and magnesium metabolism, unspecified
P721Transitory neonatal hyperthyroidism
P729Transitory neonatal endocrine disorder, unspecified
P740Late metabolic acidosis of newborn
P741Dehydration of newborn
P7421Hypernatremia of newborn
P7422Hyponatremia of newborn
P7431Hyperkalemia of newborn
P7432Hypokalemia of newborn
P7441Alkalosis of newborn
P74421Hyperchloremia of newborn
P74422Hypochloremia of newborn
P7449Other transitory electrolyte disturbance of newborn
P746Transitory hyperammonemia of newborn
P749Transitory metabolic disturbance of newborn, unspecified
P940Transient neonatal myasthenia gravis
 
PDX Collection 3464
P700Syndrome of infant of mother with gestational diabetes
P701Syndrome of infant of a diabetic mother
P702Neonatal diabetes mellitus
P703Iatrogenic neonatal hypoglycemia
P704Other neonatal hypoglycemia
P709Transitory disorder of carbohydrate metabolism of newborn, unspecified
P710Cow's milk hypocalcemia in newborn
P711Other neonatal hypocalcemia
P712Neonatal hypomagnesemia
P713Neonatal tetany without calcium or magnesium deficiency
P714Transitory neonatal hypoparathyroidism
P718Other transitory neonatal disorders of calcium and magnesium metabolism
P719Transitory neonatal disorder of calcium and magnesium metabolism, unspecified
P721Transitory neonatal hyperthyroidism
P729Transitory neonatal endocrine disorder, unspecified
P740Late metabolic acidosis of newborn
P741Dehydration of newborn
P7421Hypernatremia of newborn
P7422Hyponatremia of newborn
P7431Hyperkalemia of newborn
P7432Hypokalemia of newborn
P7441Alkalosis of newborn
P74421Hyperchloremia of newborn
P74422Hypochloremia of newborn
P7449Other transitory electrolyte disturbance of newborn
P748Other transitory metabolic disturbances of newborn
P749Transitory metabolic disturbance of newborn, unspecified
P940Transient neonatal myasthenia gravis
 
PDX Collection 3467
Q7960Ehlers-Danlos syndrome, unspecified
Q7961Classical Ehlers-Danlos syndrome
Q7962Hypermobile Ehlers-Danlos syndrome
Q7963Vascular Ehlers-Danlos syndrome
Q7969Other Ehlers-Danlos syndromes
 
PDX Collection 3485
Z1620Resistance to unspecified antibiotic
 
PDX Collection 3486
Z1622Resistance to vancomycin related antibiotics
 
PDX Collection 3487
Z1623Resistance to quinolones and fluoroquinolones
 
PDX Collection 3488
Z1629Resistance to other single specified antibiotic
 
PDX Collection 3489
Z1630Resistance to unspecified antimicrobial drugs
 
PDX Collection 3490
Z1631Resistance to antiparasitic drug(s)
 
PDX Collection 3491
Z1632Resistance to antifungal drug(s)
 
PDX Collection 3492
Z1633Resistance to antiviral drug(s)
 
PDX Collection 3493
Z16341Resistance to single antimycobacterial drug
 
PDX Collection 3494
Z16342Resistance to multiple antimycobacterial drugs
 
PDX Collection 3495
Z1635Resistance to multiple antimicrobial drugs
 
PDX Collection 3496
Z1610Resistance to unspecified beta lactam antibiotics
 
PDX Collection 3497
Z1611Resistance to penicillins
 
PDX Collection 3498
Z1619Resistance to other specified beta lactam antibiotics
 
PDX Collection 3499
E7871Barth syndrome
E7872Smith-Lemli-Opitz syndrome
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's syndrome, unspecified
Q87410Marfan's syndrome with aortic dilation
Q87418Marfan's syndrome with other cardiovascular manifestations
Q8742Marfan's syndrome with ocular manifestations
Q8743Marfan's syndrome with skeletal manifestation
Q875Other congenital malformation syndromes with other skeletal changes
Q8781Alport syndrome
Q8782Arterial tortuosity syndrome
Q8789Other specified congenital malformation syndromes, not elsewhere classified
Q898Other specified congenital malformations
Q992Fragile X chromosome
 
PDX Collection 3500
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
I234Rupture of chordae tendineae as current complication following acute myocardial infarction
I235Rupture of papillary muscle 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
I400Infective myocarditis
I401Isolated myocarditis
I408Other acute myocarditis
I409Acute myocarditis, unspecified
I41Myocarditis in diseases classified elsewhere
I510Cardiac septal defect, acquired
I511Rupture of chordae tendineae, not elsewhere classified
I512Rupture of papillary muscle, not elsewhere classified
I514Myocarditis, unspecified
I878Other specified disorders of veins
I879Disorder of vein, unspecified
I970Postcardiotomy syndrome
I97110Postprocedural cardiac insufficiency following cardiac surgery
I97111Postprocedural cardiac insufficiency following other surgery
I97120Postprocedural cardiac arrest following cardiac surgery
I97121Postprocedural cardiac arrest following other surgery
I97130Postprocedural heart failure following cardiac surgery
I97131Postprocedural heart failure following other surgery
I97190Other postprocedural cardiac functional disturbances following cardiac surgery
I97191Other postprocedural cardiac functional disturbances following other surgery
I998Other disorder of circulatory system
I999Unspecified disorder of circulatory system
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
Q211Atrial septal defect
Q212Atrioventricular 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's syndrome, unspecified
Q87410Marfan's syndrome with aortic dilation
Q87418Marfan's syndrome with other cardiovascular manifestations
Q8742Marfan's syndrome with ocular manifestations
Q8743Marfan's syndrome with skeletal manifestation
Q875Other congenital malformation syndromes with other skeletal changes
Q8781Alport syndrome
Q8782Arterial tortuosity syndrome
Q8789Other specified congenital malformation syndromes, not elsewhere classified
Q897Multiple congenital malformations, not elsewhere classified
Q898Other specified congenital malformations
Q992Fragile X chromosome
 
PDX Collection 3501
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's syndrome, unspecified
Q87410Marfan's syndrome with aortic dilation
Q87418Marfan's syndrome with other cardiovascular manifestations
Q8742Marfan's syndrome with ocular manifestations
Q8743Marfan's syndrome with skeletal manifestation
Q875Other congenital malformation syndromes with other skeletal changes
Q8781Alport syndrome
Q8782Arterial tortuosity syndrome
Q8789Other specified congenital malformation syndromes, not elsewhere classified
Q897Multiple congenital malformations, not elsewhere classified
Q898Other specified congenital malformations
Q992Fragile X chromosome
 
PDX Collection 3502
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
Q211Atrial septal defect
Q212Atrioventricular 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's syndrome, unspecified
Q87410Marfan's syndrome with aortic dilation
Q87418Marfan's syndrome with other cardiovascular manifestations
Q8742Marfan's syndrome with ocular manifestations
Q8743Marfan's syndrome with skeletal manifestation
Q875Other congenital malformation syndromes with other skeletal changes
Q8781Alport syndrome
Q8782Arterial tortuosity syndrome
Q8789Other specified congenital malformation syndromes, not elsewhere classified
Q897Multiple congenital malformations, not elsewhere classified
Q898Other specified congenital malformations
Q992Fragile X chromosome
 
PDX Collection 3503
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's syndrome, unspecified
Q87410Marfan's syndrome with aortic dilation
Q87418Marfan's syndrome with other cardiovascular manifestations
Q8742Marfan's syndrome with ocular manifestations
Q8743Marfan's syndrome with skeletal manifestation
Q875Other congenital malformation syndromes with other skeletal changes
Q8781Alport syndrome
Q8782Arterial tortuosity syndrome
Q8789Other specified congenital malformation syndromes, not elsewhere classified
Q897Multiple congenital malformations, not elsewhere classified
Q898Other specified congenital malformations
Q992Fragile X chromosome
 
PDX Collection 3504
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's syndrome, unspecified
Q87410Marfan's syndrome with aortic dilation
Q87418Marfan's syndrome with other cardiovascular manifestations
Q8742Marfan's syndrome with ocular manifestations
Q8743Marfan's syndrome with skeletal manifestation
Q875Other congenital malformation syndromes with other skeletal changes
Q8781Alport syndrome
Q8782Arterial tortuosity syndrome
Q8789Other specified congenital malformation syndromes, not elsewhere classified
Q897Multiple congenital malformations, not elsewhere classified
Q898Other specified congenital malformations
Q992Fragile X chromosome
 
PDX Collection 3505
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's syndrome, unspecified
Q87410Marfan's syndrome with aortic dilation
Q87418Marfan's syndrome with other cardiovascular manifestations
Q8742Marfan's syndrome with ocular manifestations
Q8743Marfan's syndrome with skeletal manifestation
Q875Other congenital malformation syndromes with other skeletal changes
Q8781Alport syndrome
Q8782Arterial tortuosity syndrome
Q8789Other specified congenital malformation syndromes, not elsewhere classified
Q897Multiple congenital malformations, not elsewhere classified
Q898Other specified congenital malformations
Q992Fragile X chromosome
 
PDX Collection 3506
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's syndrome, unspecified
Q87410Marfan's syndrome with aortic dilation
Q87418Marfan's syndrome with other cardiovascular manifestations
Q8742Marfan's syndrome with ocular manifestations



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