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 156 of 689
PDX Collection 1039 (continued)
D61811Other drug-induced pancytopenia
D61818Other pancytopenia
D6182Myelophthisis
D6189Other specified aplastic anemias and other bone marrow failure syndromes
D619Aplastic anemia, unspecified
D62Acute posthemorrhagic anemia
D630Anemia in neoplastic disease
D631Anemia in chronic kidney disease
D638Anemia in other chronic diseases classified elsewhere
D640Hereditary sideroblastic anemia
D641Secondary sideroblastic anemia due to disease
D642Secondary sideroblastic anemia due to drugs and toxins
D643Other sideroblastic anemias
D644Congenital dyserythropoietic anemia
D6481Anemia due to antineoplastic chemotherapy
D6489Other specified anemias
D649Anemia, unspecified
D759Disease of blood and blood-forming organs, unspecified
P612Anemia of prematurity
P613Congenital anemia from fetal blood loss
P614Other congenital anemias, not elsewhere classified
 
PDX Collection 1040
D501Sideropenic dysphagia
D508Other iron deficiency anemias
D509Iron deficiency anemia, unspecified
D510Vitamin B12 deficiency anemia due to intrinsic factor deficiency
D511Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria
D512Transcobalamin II deficiency
D513Other dietary vitamin B12 deficiency anemia
D518Other vitamin B12 deficiency anemias
D519Vitamin B12 deficiency anemia, unspecified
D520Dietary folate deficiency anemia
D521Drug-induced folate deficiency anemia
D528Other folate deficiency anemias
D529Folate deficiency anemia, unspecified
D530Protein deficiency anemia
D531Other megaloblastic anemias, not elsewhere classified
D532Scorbutic anemia
D538Other specified nutritional anemias
D539Nutritional anemia, unspecified
D564Hereditary persistence of fetal hemoglobin [HPFH]
D5700Hb-SS disease with crisis, unspecified
D5701Hb-SS disease with acute chest syndrome
D5702Hb-SS disease with splenic sequestration
D571Sickle-cell disease without crisis
D5720Sickle-cell/Hb-C disease without crisis
D573Sickle-cell trait
D57811Other sickle-cell disorders with acute chest syndrome
D57812Other sickle-cell disorders with splenic sequestration
D57819Other sickle-cell disorders with crisis, unspecified
D582Other hemoglobinopathies
D590Drug-induced autoimmune hemolytic anemia
D5910Autoimmune hemolytic anemia, unspecified
D5911Warm autoimmune hemolytic anemia
D5912Cold autoimmune hemolytic anemia
D5913Mixed type autoimmune hemolytic anemia
D5919Other autoimmune hemolytic anemia
D593Hemolytic-uremic syndrome
D600Chronic acquired pure red cell aplasia
D601Transient acquired pure red cell aplasia
D608Other acquired pure red cell aplasias
D609Acquired pure red cell aplasia, unspecified
D6101Constitutional (pure) red blood cell aplasia
D6109Other constitutional aplastic anemia
D611Drug-induced aplastic anemia
D612Aplastic anemia due to other external agents
D613Idiopathic aplastic anemia
D61810Antineoplastic chemotherapy induced pancytopenia
D61811Other drug-induced pancytopenia
D61818Other pancytopenia
D6182Myelophthisis
D6189Other specified aplastic anemias and other bone marrow failure syndromes
D619Aplastic anemia, unspecified
D630Anemia in neoplastic disease
D631Anemia in chronic kidney disease
D638Anemia in other chronic diseases classified elsewhere
D640Hereditary sideroblastic anemia
D641Secondary sideroblastic anemia due to disease
D642Secondary sideroblastic anemia due to drugs and toxins
D643Other sideroblastic anemias
D644Congenital dyserythropoietic anemia
D6481Anemia due to antineoplastic chemotherapy
D6489Other specified anemias
D649Anemia, unspecified
D759Disease of blood and blood-forming organs, unspecified
P615Transient neonatal neutropenia
P618Other specified perinatal hematological disorders
P619Perinatal hematological disorder, unspecified
 
PDX Collection 1041
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
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
P749Transitory metabolic disturbance of newborn, unspecified
P940Transient neonatal myasthenia gravis
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 1042
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
P749Transitory metabolic disturbance of newborn, unspecified
P940Transient neonatal myasthenia gravis
 
PDX Collection 1043
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 1044
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 1045
P830Sclerema neonatorum
P8330Unspecified edema specific to newborn
P8339Other edema specific to newborn
 
PDX Collection 1046
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 1047
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 1048
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
P91811Neonatal encephalopathy in diseases classified elsewhere
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 1049
P90Convulsions of newborn
P910Neonatal cerebral ischemia
P911Acquired periventricular cysts of newborn
P913Neonatal cerebral irritability
P914Neonatal cerebral depression
P915Neonatal coma
P91811Neonatal encephalopathy in diseases classified elsewhere
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 1050
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 1051
P9201Bilious vomiting of newborn
P9209Other vomiting of newborn
 
PDX Collection 1052
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 1053
Q000Anencephaly
Q001Craniorachischisis
Q002Iniencephaly
 
PDX Collection 1054
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 1055
Q044Septo-optic dysplasia of brain
Q045Megalencephaly
Q046Congenital cerebral cysts
Q048Other specified congenital malformations of brain
 
PDX Collection 1057
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
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 1058
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
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



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