ICD-10-CM/PCS MS-DRG v40.0 Definitions Manual
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DRAFT
ICD-10-CM/PCS MS-DRG v40.0 Definitions Manual |
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| Appendix C: Principal diagnoses which convert CC/MCC to non-CC |
| Page 131 of 1270 |
| PDX Collection 1041 (continued) | |
| P740 | Late metabolic acidosis of newborn |
| P741 | Dehydration of newborn |
| P7421 | Hypernatremia of newborn |
| P7422 | Hyponatremia of newborn |
| P7431 | Hyperkalemia of newborn |
| P7432 | Hypokalemia of newborn |
| P7441 | Alkalosis of newborn |
| P74421 | Hyperchloremia of newborn |
| P74422 | Hypochloremia of newborn |
| P7449 | Other transitory electrolyte disturbance of newborn |
| P749 | Transitory metabolic disturbance of newborn, unspecified |
| P940 | Transient neonatal myasthenia gravis |
| P941 | Congenital hypertonia |
| P942 | Congenital hypotonia |
| P948 | Other disorders of muscle tone of newborn |
| P949 | Disorder of muscle tone of newborn, unspecified |
| P960 | Congenital renal failure |
| P963 | Wide cranial sutures of newborn |
| P965 | Complication to newborn due to (fetal) intrauterine procedure |
| P9682 | Delayed separation of umbilical cord |
| P9683 | Meconium staining |
| P9689 | Other specified conditions originating in the perinatal period |
| PDX Collection 1042 | |
| P700 | Syndrome of infant of mother with gestational diabetes |
| P701 | Syndrome of infant of a diabetic mother |
| P702 | Neonatal diabetes mellitus |
| P703 | Iatrogenic neonatal hypoglycemia |
| P704 | Other neonatal hypoglycemia |
| P709 | Transitory disorder of carbohydrate metabolism of newborn, unspecified |
| P710 | Cow's milk hypocalcemia in newborn |
| P711 | Other neonatal hypocalcemia |
| P712 | Neonatal hypomagnesemia |
| P713 | Neonatal tetany without calcium or magnesium deficiency |
| P714 | Transitory neonatal hypoparathyroidism |
| P718 | Other transitory neonatal disorders of calcium and magnesium metabolism |
| P719 | Transitory neonatal disorder of calcium and magnesium metabolism, unspecified |
| P721 | Transitory neonatal hyperthyroidism |
| P729 | Transitory neonatal endocrine disorder, unspecified |
| P740 | Late metabolic acidosis of newborn |
| P741 | Dehydration of newborn |
| P7421 | Hypernatremia of newborn |
| P7422 | Hyponatremia of newborn |
| P7431 | Hyperkalemia of newborn |
| P7432 | Hypokalemia of newborn |
| P7441 | Alkalosis of newborn |
| P74421 | Hyperchloremia of newborn |
| P74422 | Hypochloremia of newborn |
| P7449 | Other transitory electrolyte disturbance of newborn |
| P749 | Transitory metabolic disturbance of newborn, unspecified |
| P940 | Transient neonatal myasthenia gravis |
| PDX Collection 1043 | |
| P760 | Meconium plug syndrome |
| P761 | Transitory ileus of newborn |
| P762 | Intestinal obstruction due to inspissated milk |
| P768 | Other specified intestinal obstruction of newborn |
| P769 | Intestinal obstruction of newborn, unspecified |
| P771 | Stage 1 necrotizing enterocolitis in newborn |
| P772 | Stage 2 necrotizing enterocolitis in newborn |
| P773 | Stage 3 necrotizing enterocolitis in newborn |
| P779 | Necrotizing enterocolitis in newborn, unspecified |
| P780 | Perinatal intestinal perforation |
| P781 | Other neonatal peritonitis |
| P782 | Neonatal hematemesis and melena due to swallowed maternal blood |
| P783 | Noninfective neonatal diarrhea |
| P7881 | Congenital cirrhosis (of liver) |
| P7882 | Peptic ulcer of newborn |
| P7883 | Newborn esophageal reflux |
| P7884 | Gestational alloimmune liver disease |
| P7889 | Other specified perinatal digestive system disorders |
| P789 | Perinatal digestive system disorder, unspecified |
| PDX Collection 1044 | |
| P290 | Neonatal cardiac failure |
| P2911 | Neonatal tachycardia |
| P2912 | Neonatal bradycardia |
| P292 | Neonatal hypertension |
| P294 | Transient myocardial ischemia in newborn |
| P2989 | Other cardiovascular disorders originating in the perinatal period |
| P299 | Cardiovascular disorder originating in the perinatal period, unspecified |
| P760 | Meconium plug syndrome |
| P761 | Transitory ileus of newborn |
| P762 | Intestinal obstruction due to inspissated milk |
| P768 | Other specified intestinal obstruction of newborn |
| P769 | Intestinal obstruction of newborn, unspecified |
| P771 | Stage 1 necrotizing enterocolitis in newborn |
| P772 | Stage 2 necrotizing enterocolitis in newborn |
| P773 | Stage 3 necrotizing enterocolitis in newborn |
| P779 | Necrotizing enterocolitis in newborn, unspecified |
| P780 | Perinatal intestinal perforation |
| P781 | Other neonatal peritonitis |
| P782 | Neonatal hematemesis and melena due to swallowed maternal blood |
| P783 | Noninfective neonatal diarrhea |
| P7881 | Congenital cirrhosis (of liver) |
| P7882 | Peptic ulcer of newborn |
| P7883 | Newborn esophageal reflux |
| P7884 | Gestational alloimmune liver disease |
| P7889 | Other specified perinatal digestive system disorders |
| P789 | Perinatal digestive system disorder, unspecified |
| P941 | Congenital hypertonia |
| P942 | Congenital hypotonia |
| P948 | Other disorders of muscle tone of newborn |
| P949 | Disorder of muscle tone of newborn, unspecified |
| P960 | Congenital renal failure |
| P963 | Wide cranial sutures of newborn |
| P965 | Complication to newborn due to (fetal) intrauterine procedure |
| P9682 | Delayed separation of umbilical cord |
| P9683 | Meconium staining |
| P9689 | Other specified conditions originating in the perinatal period |
| PDX Collection 1045 | |
| P830 | Sclerema neonatorum |
| P8330 | Unspecified edema specific to newborn |
| P8339 | Other edema specific to newborn |
| PDX Collection 1046 | |
| P290 | Neonatal cardiac failure |
| P2911 | Neonatal tachycardia |
| P2912 | Neonatal bradycardia |
| P292 | Neonatal hypertension |
| P294 | Transient myocardial ischemia in newborn |
| P2989 | Other cardiovascular disorders originating in the perinatal period |
| P299 | Cardiovascular disorder originating in the perinatal period, unspecified |
| P832 | Hydrops fetalis not due to hemolytic disease |
| P941 | Congenital hypertonia |
| P942 | Congenital hypotonia |
| P948 | Other disorders of muscle tone of newborn |
| P949 | Disorder of muscle tone of newborn, unspecified |
| P960 | Congenital renal failure |
| P963 | Wide cranial sutures of newborn |
| P965 | Complication to newborn due to (fetal) intrauterine procedure |
| P9682 | Delayed separation of umbilical cord |
| P9683 | Meconium staining |
| P9689 | Other specified conditions originating in the perinatal period |
| PDX Collection 1047 | |
| P800 | Cold injury syndrome |
| P808 | Other hypothermia of newborn |
| P809 | Hypothermia of newborn, unspecified |
| P810 | Environmental hyperthermia of newborn |
| P818 | Other specified disturbances of temperature regulation of newborn |
| P819 | Disturbance of temperature regulation of newborn, unspecified |
| P830 | Sclerema neonatorum |
| P8330 | Unspecified edema specific to newborn |
| P8339 | Other edema specific to newborn |
| PDX Collection 1048 | |
| P290 | Neonatal cardiac failure |
| P2911 | Neonatal tachycardia |
| P2912 | Neonatal bradycardia |
| P292 | Neonatal hypertension |
| P294 | Transient myocardial ischemia in newborn |
| P2989 | Other cardiovascular disorders originating in the perinatal period |
| P299 | Cardiovascular disorder originating in the perinatal period, unspecified |
| P90 | Convulsions of newborn |
| P91811 | Neonatal encephalopathy in diseases classified elsewhere |
| P91819 | Neonatal encephalopathy, unspecified |
| P91821 | Neonatal cerebral infarction, right side of brain |
| P91822 | Neonatal cerebral infarction, left side of brain |
| P91823 | Neonatal cerebral infarction, bilateral |
| P91829 | Neonatal cerebral infarction, unspecified side |
| P9188 | Other specified disturbances of cerebral status of newborn |
| P919 | Disturbance of cerebral status of newborn, unspecified |
| P941 | Congenital hypertonia |
| P942 | Congenital hypotonia |
| P948 | Other disorders of muscle tone of newborn |
| P949 | Disorder of muscle tone of newborn, unspecified |
| P960 | Congenital renal failure |
| P963 | Wide cranial sutures of newborn |
| P965 | Complication to newborn due to (fetal) intrauterine procedure |
| P9682 | Delayed separation of umbilical cord |
| P9683 | Meconium staining |
| P9689 | Other specified conditions originating in the perinatal period |
| PDX Collection 1049 | |
| P90 | Convulsions of newborn |
| P910 | Neonatal cerebral ischemia |
| P911 | Acquired periventricular cysts of newborn |
| P913 | Neonatal cerebral irritability |
| P914 | Neonatal cerebral depression |
| P915 | Neonatal coma |
| P91811 | Neonatal encephalopathy in diseases classified elsewhere |
| P91819 | Neonatal encephalopathy, unspecified |
| P91821 | Neonatal cerebral infarction, right side of brain |
| P91822 | Neonatal cerebral infarction, left side of brain |
| P91823 | Neonatal cerebral infarction, bilateral |
| P91829 | Neonatal cerebral infarction, unspecified side |
| P9188 | Other specified disturbances of cerebral status of newborn |
| P919 | Disturbance of cerebral status of newborn, unspecified |
| PDX Collection 1050 | |
| P84 | Other problems with newborn |
| P9160 | Hypoxic ischemic encephalopathy [HIE], unspecified |
| P9161 | Mild hypoxic ischemic encephalopathy [HIE] |
| P9162 | Moderate hypoxic ischemic encephalopathy [HIE] |
| P9163 | Severe hypoxic ischemic encephalopathy [HIE] |
| PDX Collection 1051 | |
| P9201 | Bilious vomiting of newborn |
| P9209 | Other vomiting of newborn |
| PDX Collection 1052 | |
| P930 | Grey baby syndrome |
| P938 | Other reactions and intoxications due to drugs administered to newborn |
| P961 | Neonatal withdrawal symptoms from maternal use of drugs of addiction |
| P962 | Withdrawal symptoms from therapeutic use of drugs in newborn |
| PDX Collection 1053 | |
| Q000 | Anencephaly |
| Q001 | Craniorachischisis |
| Q002 | Iniencephaly |
| PDX Collection 1054 | |
| Q010 | Frontal encephalocele |
| Q011 | Nasofrontal encephalocele |
| Q012 | Occipital encephalocele |
| Q018 | Encephalocele of other sites |
| Q019 | Encephalocele, unspecified |
| Q02 | Microcephaly |
| Q040 | Congenital malformations of corpus callosum |
| Q041 | Arhinencephaly |
| Q042 | Holoprosencephaly |
| Q043 | Other reduction deformities of brain |
| Q044 | Septo-optic dysplasia of brain |
| Q045 | Megalencephaly |
| Q046 | Congenital cerebral cysts |
| Q048 | Other specified congenital malformations of brain |
| PDX Collection 1055 | |
| Q044 | Septo-optic dysplasia of brain |
| Q045 | Megalencephaly |
| Q046 | Congenital cerebral cysts |
| Q048 | Other specified congenital malformations of brain |
| PDX Collection 1060 | |
| E7871 | Barth syndrome |
| E7872 | Smith-Lemli-Opitz syndrome |
| Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
| Q220 | Pulmonary valve atresia |
| Q221 | Congenital pulmonary valve stenosis |
| Q222 | Congenital pulmonary valve insufficiency |
| Q223 | Other congenital malformations of pulmonary valve |
| Q238 | Other congenital malformations of aortic and mitral valves |
| Q239 | Congenital malformation of aortic and mitral valves, unspecified |
| Q248 | Other specified congenital malformations of heart |
| Q249 | Congenital malformation of heart, unspecified |
| Q2730 | Arteriovenous malformation, site unspecified |
| Q274 | Congenital phlebectasia |
| Q280 | Arteriovenous malformation of precerebral vessels |
| Q281 | Other malformations of precerebral vessels |
| Q288 | Other specified congenital malformations of circulatory system |
| Q289 | Congenital malformation of circulatory system, unspecified |
| Q872 | Congenital malformation syndromes predominantly involving limbs |
| Q873 | Congenital malformation syndromes involving early overgrowth |
| Q875 | Other congenital malformation syndromes with other skeletal changes |
| Q8781 | Alport syndrome |
| Q8782 | Arterial tortuosity syndrome |
| Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
| Q897 | Multiple congenital malformations, not elsewhere classified |
| Q898 | Other specified congenital malformations |
| PDX Collection 1061 | |
| E7871 | Barth syndrome |
| E7872 | Smith-Lemli-Opitz syndrome |
| P2930 | Pulmonary hypertension of newborn |
| P2938 | Other persistent fetal circulation |
| Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
| Q224 | Congenital tricuspid stenosis |
| Q225 | Ebstein's anomaly |
| Q226 | Hypoplastic right heart syndrome |
| Q228 | Other congenital malformations of tricuspid valve |
| Q229 | Congenital malformation of tricuspid valve, unspecified |
| Q230 | Congenital stenosis of aortic valve |
| Q231 | Congenital insufficiency of aortic valve |
| Q232 | Congenital mitral stenosis |
| Q233 | Congenital mitral insufficiency |
| Q234 | Hypoplastic left heart syndrome |
| Q238 | Other congenital malformations of aortic and mitral valves |
| Q239 | Congenital malformation of aortic and mitral valves, unspecified |
| Q248 | Other specified congenital malformations of heart |
| Q249 | Congenital malformation of heart, unspecified |
| Q2730 | Arteriovenous malformation, site unspecified |
| Q274 | Congenital phlebectasia |
| Q280 | Arteriovenous malformation of precerebral vessels |
| Q281 | Other malformations of precerebral vessels |
| Q288 | Other specified congenital malformations of circulatory system |
| Q289 | Congenital malformation of circulatory system, unspecified |
| Q872 | Congenital malformation syndromes predominantly involving limbs |
| Q873 | Congenital malformation syndromes involving early overgrowth |
| Q8740 | Marfan's syndrome, unspecified |
| Q87410 | Marfan's syndrome with aortic dilation |
| Q87418 | Marfan's syndrome with other cardiovascular manifestations |
| Q8742 | Marfan's syndrome with ocular manifestations |
| Q8743 | Marfan's syndrome with skeletal manifestation |
| Q875 | Other congenital malformation syndromes with other skeletal changes |
| Q8781 | Alport syndrome |
| Q8782 | Arterial tortuosity syndrome |
| Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
| Q897 | Multiple congenital malformations, not elsewhere classified |
| Q898 | Other specified congenital malformations |
| Q992 | Fragile X chromosome |
| PDX Collection 1062 | |
| E7871 | Barth syndrome |
| E7872 | Smith-Lemli-Opitz syndrome |
| Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
| Q238 | Other congenital malformations of aortic and mitral valves |
| Q239 | Congenital malformation of aortic and mitral valves, unspecified |
| Q240 | Dextrocardia |
| Q241 | Levocardia |
| Q242 | Cor triatriatum |
| Q243 | Pulmonary infundibular stenosis |
| Q244 | Congenital subaortic stenosis |
| Q248 | Other specified congenital malformations of heart |
| Q249 | Congenital malformation of heart, unspecified |
| Q2730 | Arteriovenous malformation, site unspecified |
| Q274 | Congenital phlebectasia |
| Q280 | Arteriovenous malformation of precerebral vessels |
| Q281 | Other malformations of precerebral vessels |
| Q288 | Other specified congenital malformations of circulatory system |
| Q289 | Congenital malformation of circulatory system, unspecified |
| Q872 | Congenital malformation syndromes predominantly involving limbs |
| Q873 | Congenital malformation syndromes involving early overgrowth |
| Q875 | Other congenital malformation syndromes with other skeletal changes |
| Q8781 | Alport syndrome |
| Q8782 | Arterial tortuosity syndrome |
| Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
| Q897 | Multiple congenital malformations, not elsewhere classified |
| Q898 | Other specified congenital malformations |
| PDX Collection 1064 | |
| Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
| Q238 | Other congenital malformations of aortic and mitral valves |
| Q239 | Congenital malformation of aortic and mitral valves, unspecified |
| Q245 | Malformation of coronary vessels |
| Q248 | Other specified congenital malformations of heart |
| Q249 | Congenital malformation of heart, unspecified |
| PDX Collection 1066 | |
| Q250 | Patent ductus arteriosus |
| Q2730 | Arteriovenous malformation, site unspecified |
| Q274 | Congenital phlebectasia |
| Q280 | Arteriovenous malformation of precerebral vessels |
| Q281 | Other malformations of precerebral vessels |
| Q288 | Other specified congenital malformations of circulatory system |
| PDX Collection 1067 | |
| E7871 | Barth syndrome |
| E7872 | Smith-Lemli-Opitz syndrome |
| Q251 | Coarctation of aorta |
| Q2521 | Interruption of aortic arch |
| Q2529 | Other atresia of aorta |
| Q253 | Supravalvular aortic stenosis |
| Q2730 | Arteriovenous malformation, site unspecified |
| Q274 | Congenital phlebectasia |
| Q280 | Arteriovenous malformation of precerebral vessels |
| Q281 | Other malformations of precerebral vessels |
| Q288 | Other specified congenital malformations of circulatory system |
| Q289 | Congenital malformation of circulatory system, unspecified |
| Q872 | Congenital malformation syndromes predominantly involving limbs |
| Q873 | Congenital malformation syndromes involving early overgrowth |
| Q875 | Other congenital malformation syndromes with other skeletal changes |
| Q8781 | Alport syndrome |
| Q8782 | Arterial tortuosity syndrome |
| Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
| Q897 | Multiple congenital malformations, not elsewhere classified |
| Q898 | Other specified congenital malformations |
| PDX Collection 1069 | |
| E7871 | Barth syndrome |
| E7872 | Smith-Lemli-Opitz syndrome |
| Q251 | Coarctation of aorta |
| Q2521 | Interruption of aortic arch |
| Q2529 | Other atresia of aorta |
| Q253 | Supravalvular aortic stenosis |
| Q2540 | Congenital malformation of aorta unspecified |
| Q2541 | Absence and aplasia of aorta |
| Q2542 | Hypoplasia of aorta |
| Q2543 | Congenital aneurysm of aorta |
| Q2544 | Congenital dilation of aorta |
| Q2545 | Double aortic arch |
| Q2546 | Tortuous aortic arch |
| Q2547 | Right aortic arch |
| Q2548 | Anomalous origin of subclavian artery |
| Q2549 | Other congenital malformations of aorta |
| Q258 | Other congenital malformations of other great arteries |
| Q259 | Congenital malformation of great arteries, unspecified |
| Q2730 | Arteriovenous malformation, site unspecified |
| Q274 | Congenital phlebectasia |
| Q280 | Arteriovenous malformation of precerebral vessels |
| Q281 | Other malformations of precerebral vessels |
| Q288 | Other specified congenital malformations of circulatory system |
| Q289 | Congenital malformation of circulatory system, unspecified |
| Q872 | Congenital malformation syndromes predominantly involving limbs |
| Q873 | Congenital malformation syndromes involving early overgrowth |
| Q875 | Other congenital malformation syndromes with other skeletal changes |
| Q8781 | Alport syndrome |
| Q8782 | Arterial tortuosity syndrome |
| Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
| Q897 | Multiple congenital malformations, not elsewhere classified |
| Q898 | Other specified congenital malformations |
| PDX Collection 1070 | |
| Q255 | Atresia of pulmonary artery |
| Q256 | Stenosis of pulmonary artery |
| Q2571 | Coarctation of pulmonary artery |
| Q2572 | Congenital pulmonary arteriovenous malformation |
| Q2579 | Other congenital malformations of pulmonary artery |
| Q2730 | Arteriovenous malformation, site unspecified |
| Q274 | Congenital phlebectasia |
| Q280 | Arteriovenous malformation of precerebral vessels |
| Q281 | Other malformations of precerebral vessels |
| Q288 | Other specified congenital malformations of circulatory system |
| Q289 | Congenital malformation of circulatory system, unspecified |
| PDX Collection 1071 | |
| Q260 | Congenital stenosis of vena cava |
| Q261 | Persistent left superior vena cava |
| Q268 | Other congenital malformations of great veins |
| Q2730 | Arteriovenous malformation, site unspecified |
| Q274 | Congenital phlebectasia |
| Q280 | Arteriovenous malformation of precerebral vessels |
| Q281 | Other malformations of precerebral vessels |
| Q288 | Other specified congenital malformations of circulatory system |
| Q289 | Congenital malformation of circulatory system, unspecified |
| PDX Collection 1072 | |
| Q262 | Total anomalous pulmonary venous connection |
| Q2730 | Arteriovenous malformation, site unspecified |
| Q274 | Congenital phlebectasia |
| Q280 | Arteriovenous malformation of precerebral vessels |
| Q281 | Other malformations of precerebral vessels |
| Q288 | Other specified congenital malformations of circulatory system |
| Q289 | Congenital malformation of circulatory system, unspecified |
| PDX Collection 1073 | |
| Q263 | Partial anomalous pulmonary venous connection |
| Q264 | Anomalous pulmonary venous connection, unspecified |
| Q2730 | Arteriovenous malformation, site unspecified |
| Q274 | Congenital phlebectasia |
| Q280 | Arteriovenous malformation of precerebral vessels |
| Q281 | Other malformations of precerebral vessels |
| Q288 | Other specified congenital malformations of circulatory system |
| Q289 | Congenital malformation of circulatory system, unspecified |
| PDX Collection 1074 | |
| Q269 | Congenital malformation of great vein, unspecified |
| Q2730 | Arteriovenous malformation, site unspecified |
| Q274 | Congenital phlebectasia |
| Q280 | Arteriovenous malformation of precerebral vessels |
| Q281 | Other malformations of precerebral vessels |
| Q288 | Other specified congenital malformations of circulatory system |
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