DRAFT
ICD-10-CM/PCS MS-DRG v41.0 Definitions Manual |
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Part 1: List of CC and Major CC codes |
Page 18 of 46 |
A000 A8183 C229 C8292 D613 F0394 G40823 H5988 I70368 J157 K7111 L97526 M4857XA M84477A M8669 N184 O364XX1 P3610 R402211 S0633AA S13101A S25309A S32434K S37022A S42309P S45012A S52101Q S52261C S52363B S52611P S62031P S62344K S65311A S72065C S72324Q S72431K S76829A S82109M S82232A S82435Q S82856M S89321K S92341P T24322A T81506A T85694A |
Dx | CC/MCC | Exclusions | Description |
---|---|---|---|
P3610 | MCC | 1031:48 codes | Sepsis of newborn due to unspecified streptococci |
P3619 | MCC | 1031:48 codes | Sepsis of newborn due to other streptococci |
P362 | MCC | 1031:48 codes | Sepsis of newborn due to Staphylococcus aureus |
P3630 | MCC | 1031:48 codes | Sepsis of newborn due to unspecified staphylococci |
P3639 | MCC | 1031:48 codes | Sepsis of newborn due to other staphylococci |
P364 | MCC | 1031:48 codes | Sepsis of newborn due to Escherichia coli |
P365 | MCC | 1031:48 codes | Sepsis of newborn due to anaerobes |
P368 | MCC | 1031:48 codes | Other bacterial sepsis of newborn |
P369 | MCC | 1031:48 codes | Bacterial sepsis of newborn, unspecified |
P370 | MCC | 4049:194 codes | Congenital tuberculosis |
P371 | MCC | 0562:192 codes | Congenital toxoplasmosis |
P372 | MCC | 0562:192 codes | Neonatal (disseminated) listeriosis |
P373 | MCC | 0562:192 codes | Congenital falciparum malaria |
P374 | MCC | 0562:192 codes | Other congenital malaria |
P378 | MCC | 0562:192 codes | Other specified congenital infectious and parasitic diseases |
P379 | MCC | 0562:192 codes | Congenital infectious or parasitic disease, unspecified |
P381 | CC | 3961:5 codes | Omphalitis with mild hemorrhage |
P389 | CC | 3963:5 codes | Omphalitis without hemorrhage |
P390 | CC | 1032:5 codes | Neonatal infective mastitis |
P392 | CC | 6589:71 codes | Intra-amniotic infection affecting newborn, not elsewhere classified |
P393 | CC | 5331:55 codes | Neonatal urinary tract infection |
P394 | CC | 6593:71 codes | Neonatal skin infection |
P398 | CC | 6638:71 codes | Other specified infections specific to the perinatal period |
P399 | CC | 6636:71 codes | Infection specific to the perinatal period, unspecified |
P520 | CC | 1021:48 codes | Intraventricular (nontraumatic) hemorrhage, grade 1, of newborn |
P521 | CC | 1021:48 codes | Intraventricular (nontraumatic) hemorrhage, grade 2, of newborn |
P5221 | MCC | 1021:48 codes | Intraventricular (nontraumatic) hemorrhage, grade 3, of newborn |
P5222 | MCC | 1021:48 codes | Intraventricular (nontraumatic) hemorrhage, grade 4, of newborn |
P523 | CC | 1021:48 codes | Unspecified intraventricular (nontraumatic) hemorrhage of newborn |
P524 | MCC | 1020:39 codes | Intracerebral (nontraumatic) hemorrhage of newborn |
P525 | MCC | 1022:49 codes | Subarachnoid (nontraumatic) hemorrhage of newborn |
P526 | MCC | 1020:39 codes | Cerebellar (nontraumatic) and posterior fossa hemorrhage of newborn |
P528 | MCC | 1020:39 codes | Other intracranial (nontraumatic) hemorrhages of newborn |
P529 | MCC | 1020:39 codes | Intracranial (nontraumatic) hemorrhage of newborn, unspecified |
P53 | CC | 1035:28 codes | Hemorrhagic disease of newborn |
P541 | MCC | 1036:44 codes | Neonatal melena |
P542 | MCC | 1036:44 codes | Neonatal rectal hemorrhage |
P543 | MCC | 1036:44 codes | Other neonatal gastrointestinal hemorrhage |
P544 | CC | 1036:44 codes | Neonatal adrenal hemorrhage |
P560 | MCC | 1037:25 codes | Hydrops fetalis due to isoimmunization |
P5690 | MCC | 1037:25 codes | Hydrops fetalis due to unspecified hemolytic disease |
P5699 | MCC | 1037:25 codes | Hydrops fetalis due to other hemolytic disease |
P570 | MCC | 1037:25 codes | Kernicterus due to isoimmunization |
P578 | MCC | 1038:35 codes | Other specified kernicterus |
P579 | MCC | 1038:35 codes | Kernicterus, unspecified |
P591 | MCC | 1038:35 codes | Inspissated bile syndrome |
P5920 | MCC | 1038:35 codes | Neonatal jaundice from unspecified hepatocellular damage |
P5929 | MCC | 1038:35 codes | Neonatal jaundice from other hepatocellular damage |
P60 | MCC | 1035:28 codes | Disseminated intravascular coagulation of newborn |
P610 | MCC | 1035:28 codes | Transient neonatal thrombocytopenia |
P612 | CC | 6832:94 codes | Anemia of prematurity |
P613 | CC | 6836:94 codes | Congenital anemia from fetal blood loss |
P614 | CC | 6835:96 codes | Other congenital anemias, not elsewhere classified |
P615 | MCC | 6837:70 codes | Transient neonatal neutropenia |
P616 | CC | 5722:32 codes | Other transient neonatal disorders of coagulation |
P702 | CC | 1041:44 codes | Neonatal diabetes mellitus |
P708 | CC | 3458:28 codes | Other transitory disorders of carbohydrate metabolism of newborn |
P710 | CC | 1041:44 codes | Cow's milk hypocalcemia in newborn |
P711 | CC | 1041:44 codes | Other neonatal hypocalcemia |
P712 | CC | 1041:44 codes | Neonatal hypomagnesemia |
P713 | CC | 1041:44 codes | Neonatal tetany without calcium or magnesium deficiency |
P714 | CC | 1041:44 codes | Transitory neonatal hypoparathyroidism |
P718 | CC | 1041:44 codes | Other transitory neonatal disorders of calcium and magnesium metabolism |
P719 | CC | 1041:44 codes | Transitory neonatal disorder of calcium and magnesium metabolism, unspecified |
P720 | CC | 3459:28 codes | Neonatal goiter, not elsewhere classified |
P721 | CC | 1041:44 codes | Transitory neonatal hyperthyroidism |
P722 | CC | 3460:28 codes | Other transitory neonatal disorders of thyroid function, not elsewhere classified |
P728 | CC | 3461:28 codes | Other specified transitory neonatal endocrine disorders |
P740 | MCC | 1041:44 codes | Late metabolic acidosis of newborn |
P7441 | CC | 1042:27 codes | Alkalosis of newborn |
P745 | CC | 3462:28 codes | Transitory tyrosinemia of newborn |
P746 | CC | 3463:28 codes | Transitory hyperammonemia of newborn |
P748 | CC | 3464:28 codes | Other transitory metabolic disturbances of newborn |
P761 | CC | 1043:19 codes | Transitory ileus of newborn |
P771 | MCC | 1044:36 codes | Stage 1 necrotizing enterocolitis in newborn |
P772 | MCC | 1044:36 codes | Stage 2 necrotizing enterocolitis in newborn |
P773 | MCC | 1044:36 codes | Stage 3 necrotizing enterocolitis in newborn |
P779 | MCC | 1044:36 codes | Necrotizing enterocolitis in newborn, unspecified |
P780 | MCC | 1044:36 codes | Perinatal intestinal perforation |
P830 | CC | 1045:3 codes | Sclerema neonatorum |
P832 | MCC | 1046:18 codes | Hydrops fetalis not due to hemolytic disease |
P8330 | CC | 1047:9 codes | Unspecified edema specific to newborn |
P8339 | CC | 1047:9 codes | Other edema specific to newborn |
P90 | MCC | 1048:26 codes | Convulsions of newborn |
P910 | MCC | 1049:14 codes | Neonatal cerebral ischemia |
P911 | MCC | 1049:14 codes | Acquired periventricular cysts of newborn |
P912 | MCC | 1022:49 codes | Neonatal cerebral leukomalacia |
P913 | MCC | 1049:14 codes | Neonatal cerebral irritability |
P914 | MCC | 1049:14 codes | Neonatal cerebral depression |
P915 | MCC | 1049:14 codes | Neonatal coma |
P9160 | CC | 1050:5 codes | Hypoxic ischemic encephalopathy [HIE], unspecified |
P9161 | CC | 1050:5 codes | Mild hypoxic ischemic encephalopathy [HIE] |
P9162 | CC | 1050:5 codes | Moderate hypoxic ischemic encephalopathy [HIE] |
P9163 | MCC | 1050:5 codes | Severe hypoxic ischemic encephalopathy [HIE] |
P91821 | MCC | 4083:4 codes | Neonatal cerebral infarction, right side of brain |
P91822 | MCC | 4083:4 codes | Neonatal cerebral infarction, left side of brain |
P91823 | MCC | 4083:4 codes | Neonatal cerebral infarction, bilateral |
P91829 | MCC | 4083:4 codes | Neonatal cerebral infarction, unspecified side |
P9201 | MCC | 1051:2 codes | Bilious vomiting of newborn |
P930 | CC | 1052:4 codes | Grey baby syndrome |
P938 | CC | 1052:4 codes | Other reactions and intoxications due to drugs administered to newborn |
P940 | CC | 1041:44 codes | Transient neonatal myasthenia gravis |
P961 | CC | 1052:4 codes | Neonatal withdrawal symptoms from maternal use of drugs of addiction |
P962 | CC | 1052:4 codes | Withdrawal symptoms from therapeutic use of drugs in newborn |
Q000 | MCC | 1053:3 codes | Anencephaly |
Q001 | MCC | 1053:3 codes | Craniorachischisis |
Q002 | MCC | 1053:3 codes | Iniencephaly |
Q010 | CC | 1054:14 codes | Frontal encephalocele |
Q011 | CC | 1054:14 codes | Nasofrontal encephalocele |
Q012 | CC | 1054:14 codes | Occipital encephalocele |
Q018 | CC | 1054:14 codes | Encephalocele of other sites |
Q019 | CC | 1054:14 codes | Encephalocele, unspecified |
Q040 | MCC | 1054:14 codes | Congenital malformations of corpus callosum |
Q041 | MCC | 1054:14 codes | Arhinencephaly |
Q042 | MCC | 1054:14 codes | Holoprosencephaly |
Q043 | MCC | 1054:14 codes | Other reduction deformities of brain |
Q044 | CC | 1055:4 codes | Septo-optic dysplasia of brain |
Q045 | CC | 1055:4 codes | Megalencephaly |
Q046 | CC | 1055:4 codes | Congenital cerebral cysts |
Q048 | CC | 1055:4 codes | Other specified congenital malformations of brain |
Q050 | CC | 6688:43 codes | Cervical spina bifida with hydrocephalus |
Q051 | CC | 6687:43 codes | Thoracic spina bifida with hydrocephalus |
Q052 | CC | 6685:43 codes | Lumbar spina bifida with hydrocephalus |
Q053 | CC | 6684:43 codes | Sacral spina bifida with hydrocephalus |
Q054 | CC | 6686:43 codes | Unspecified spina bifida with hydrocephalus |
Q0702 | CC | 6363:43 codes | Arnold-Chiari syndrome with hydrocephalus |
Q0703 | CC | 6365:43 codes | Arnold-Chiari syndrome with spina bifida and hydrocephalus |
Q200 | MCC | 6543:67 codes | Common arterial trunk |
Q201 | MCC | 6551:67 codes | Double outlet right ventricle |
Q202 | MCC | 6549:67 codes | Double outlet left ventricle |
Q203 | MCC | 6539:67 codes | Discordant ventriculoarterial connection |
Q204 | MCC | 6536:67 codes | Double inlet ventricle |
Q205 | CC | 6542:67 codes | Discordant atrioventricular connection |
Q210 | CC | 6525:65 codes | Ventricular septal defect |
Q2110 | CC | 5425:49 codes | Atrial septal defect, unspecified |
Q2111 | CC | 5436:49 codes | Secundum atrial septal defect |
Q2112 | CC | 5437:49 codes | Patent foramen ovale |
Q2113 | CC | 5439:49 codes | Coronary sinus atrial septal defect |
Q2114 | CC | 5440:49 codes | Superior sinus venosus atrial septal defect |
Q2115 | CC | 5434:49 codes | Inferior sinus venosus atrial septal defect |
Q2116 | CC | 5435:49 codes | Sinus venosus atrial septal defect, unspecified |
Q2119 | CC | 5433:49 codes | Other specified atrial septal defect |
Q2120 | CC | 5322:58 codes | Atrioventricular septal defect, unspecified as to partial or complete |
Q2121 | CC | 5323:58 codes | Partial atrioventricular septal defect |
Q2122 | CC | 5332:58 codes | Transitional atrioventricular septal defect |
Q2123 | CC | 5334:58 codes | Complete atrioventricular septal defect |
Q213 | MCC | 6527:67 codes | Tetralogy of Fallot |
Q220 | MCC | 6532:38 codes | Pulmonary valve atresia |
Q221 | CC | 6601:38 codes | Congenital pulmonary valve stenosis |
Q222 | CC | 6599:28 codes | Congenital pulmonary valve insufficiency |
Q223 | CC | 6605:28 codes | Other congenital malformations of pulmonary valve |
Q224 | MCC | 6603:44 codes | Congenital tricuspid stenosis |
Q225 | MCC | 6597:44 codes | Ebstein's anomaly |
Q226 | MCC | 6596:44 codes | Hypoplastic right heart syndrome |
Q228 | MCC | 6598:44 codes | Other congenital malformations of tricuspid valve |
Q229 | MCC | 6611:44 codes | Congenital malformation of tricuspid valve, unspecified |
Q230 | CC | 6615:42 codes | Congenital stenosis of aortic valve |
Q231 | CC | 6614:42 codes | Congenital insufficiency of aortic valve |
Q232 | CC | 6578:42 codes | Congenital mitral stenosis |
Q233 | CC | 6577:42 codes | Congenital mitral insufficiency |
Q234 | MCC | 6581:44 codes | Hypoplastic left heart syndrome |
Q240 | CC | 6588:29 codes | Dextrocardia |
Q241 | CC | 6594:29 codes | Levocardia |
Q242 | MCC | 6591:37 codes | Cor triatriatum |
Q243 | CC | 6635:37 codes | Pulmonary infundibular stenosis |
Q244 | MCC | 6634:37 codes | Congenital subaortic stenosis |
Q245 | CC | 1064:6 codes | Malformation of coronary vessels |
Q246 | MCC | 6637:35 codes | Congenital heart block |
Q250 | CC | 1066:6 codes | Patent ductus arteriosus |
Q251 | CC | 6639:23 codes | Coarctation of aorta |
Q2521 | CC | 6428:33 codes | Interruption of aortic arch |
Q2529 | CC | 6425:33 codes | Other atresia of aorta |
Q253 | CC | 6640:33 codes | Supravalvular aortic stenosis |
Q2540 | CC | 6459:35 codes | Congenital malformation of aorta unspecified |
Q2541 | CC | 6461:35 codes | Absence and aplasia of aorta |
Q2542 | CC | 6462:35 codes | Hypoplasia of aorta |
Q2543 | CC | 6463:35 codes | Congenital aneurysm of aorta |
Q2544 | CC | 6453:35 codes | Congenital dilation of aorta |
Q2545 | CC | 6454:35 codes | Double aortic arch |
Q2546 | CC | 6455:35 codes | Tortuous aortic arch |
Q2547 | CC | 6458:35 codes | Right aortic arch |
Q2548 | CC | 6451:35 codes | Anomalous origin of subclavian artery |
Q2549 | CC | 6452:35 codes | Other congenital malformations of aorta |
Q255 | MCC | 1070:11 codes | Atresia of pulmonary artery |
Q256 | MCC | 1070:11 codes | Stenosis of pulmonary artery |
Q2571 | MCC | 1070:11 codes | Coarctation of pulmonary artery |
Q2572 | MCC | 1070:11 codes | Congenital pulmonary arteriovenous malformation |
Q2579 | MCC | 1070:11 codes | Other congenital malformations of pulmonary artery |
Q258 | CC | 6617:35 codes | Other congenital malformations of other great arteries |
Q259 | CC | 6616:35 codes | Congenital malformation of great arteries, unspecified |
Q260 | CC | 1071:9 codes | Congenital stenosis of vena cava |
Q261 | CC | 1071:9 codes | Persistent left superior vena cava |
Q262 | CC | 1072:7 codes | Total anomalous pulmonary venous connection |
Q263 | CC | 1073:8 codes | Partial anomalous pulmonary venous connection |
Q264 | CC | 1073:8 codes | Anomalous pulmonary venous connection, unspecified |
Q268 | CC | 1071:9 codes | Other congenital malformations of great veins |
Q269 | CC | 1074:7 codes | Congenital malformation of great vein, unspecified |
Q2730 | CC | 5275:30 codes | Arteriovenous malformation, site unspecified |
Q274 | CC | 5402:30 codes | Congenital phlebectasia |
Q280 | CC | 5382:30 codes | Arteriovenous malformation of precerebral vessels |
Q281 | CC | 5385:30 codes | Other malformations of precerebral vessels |
Q282 | MCC | 1076:8 codes | Arteriovenous malformation of cerebral vessels |
Q283 | MCC | 1076:8 codes | Other malformations of cerebral vessels |
Q288 | CC | 5426:30 codes | Other specified congenital malformations of circulatory system |
Q289 | CC | 5427:100 codes | Congenital malformation of circulatory system, unspecified |
Q311 | CC | 1078:18 codes | Congenital subglottic stenosis |
Q312 | CC | 1078:18 codes | Laryngeal hypoplasia |
Q313 | CC | 1078:18 codes | Laryngocele |
Q315 | CC | 1078:18 codes | Congenital laryngomalacia |
Q318 | CC | 1078:18 codes | Other congenital malformations of larynx |
Q319 | CC | 1078:18 codes | Congenital malformation of larynx, unspecified |
Q320 | CC | 1078:18 codes | Congenital tracheomalacia |
Q321 | CC | 1078:18 codes | Other congenital malformations of trachea |
Q322 | CC | 1078:18 codes | Congenital bronchomalacia |
Q323 | CC | 1078:18 codes | Congenital stenosis of bronchus |
Q324 | CC | 1078:18 codes | Other congenital malformations of bronchus |
Q330 | CC | 1079:13 codes | Congenital cystic lung |
Q332 | MCC | 1079:13 codes | Sequestration of lung |
Q333 | MCC | 1079:13 codes | Agenesis of lung |
Q334 | CC | 6990:14 codes | Congenital bronchiectasis |
Q336 | MCC | 1079:13 codes | Congenital hypoplasia and dysplasia of lung |
Q390 | MCC | 1081:11 codes | Atresia of esophagus without fistula |
Q391 | MCC | 1081:11 codes | Atresia of esophagus with tracheo-esophageal fistula |
Q392 | MCC | 1081:11 codes | Congenital tracheo-esophageal fistula without atresia |
Q393 | MCC | 1081:11 codes | Congenital stenosis and stricture of esophagus |
Q394 | MCC | 1081:11 codes | Esophageal web |
Q395 | CC | 1082:6 codes | Congenital dilatation of esophagus |
Q396 | CC | 1082:6 codes | Congenital diverticulum of esophagus |
Q398 | CC | 1082:6 codes | Other congenital malformations of esophagus |
Q399 | CC | 1082:6 codes | Congenital malformation of esophagus, unspecified |
Q410 | CC | 1083:7 codes | Congenital absence, atresia and stenosis of duodenum |
Q411 | CC | 1083:7 codes | Congenital absence, atresia and stenosis of jejunum |
Q412 | CC | 1083:7 codes | Congenital absence, atresia and stenosis of ileum |
Q418 | CC | 1083:7 codes | Congenital absence, atresia and stenosis of other specified parts of small intestine |
Q419 | CC | 1083:7 codes | Congenital absence, atresia and stenosis of small intestine, part unspecified |
Q420 | CC | 1084:8 codes | Congenital absence, atresia and stenosis of rectum with fistula |
Q421 | CC | 1084:8 codes | Congenital absence, atresia and stenosis of rectum without fistula |
Q422 | CC | 1084:8 codes | Congenital absence, atresia and stenosis of anus with fistula |
Q423 | CC | 1084:8 codes | Congenital absence, atresia and stenosis of anus without fistula |
Q428 | CC | 1084:8 codes | Congenital absence, atresia and stenosis of other parts of large intestine |
Q429 | CC | 1084:8 codes | Congenital absence, atresia and stenosis of large intestine, part unspecified |
Q431 | CC | 1085:4 codes | Hirschsprung's disease |
Q432 | CC | 1085:4 codes | Other congenital functional disorders of colon |
Q433 | CC | 1086:7 codes | Congenital malformations of intestinal fixation |
Q434 | CC | 1087:21 codes | Duplication of intestine |
Q435 | CC | 1087:21 codes | Ectopic anus |
Q436 | CC | 1087:21 codes | Congenital fistula of rectum and anus |
Q437 | CC | 1087:21 codes | Persistent cloaca |
Q438 | CC | 1087:21 codes | Other specified congenital malformations of intestine |
Q439 | CC | 1087:21 codes | Congenital malformation of intestine, unspecified |
Q440 | CC | 6505:10 codes | Agenesis, aplasia and hypoplasia of gallbladder |
Q441 | CC | 6544:10 codes | Other congenital malformations of gallbladder |
Q442 | MCC | 1089:4 codes | Atresia of bile ducts |
Q443 | MCC | 1089:4 codes | Congenital stenosis and stricture of bile ducts |
Q444 | CC | 6548:10 codes | Choledochal cyst |
Q445 | CC | 6538:10 codes | Other congenital malformations of bile ducts |
Q446 | CC | 6535:8 codes | Cystic disease of liver |
Q4470 | CC | 6257:10 codes | Other congenital malformation of liver, unspecified |
Q4471 | CC | 6254:10 codes | Alagille syndrome |
Q4479 | CC | 6271:10 codes | Other congenital malformations of liver |
Q450 | CC | 1091:6 codes | Agenesis, aplasia and hypoplasia of pancreas |
Q451 | CC | 1091:6 codes | Annular pancreas |
Q452 | CC | 1091:6 codes | Congenital pancreatic cyst |
Q453 | CC | 1091:6 codes | Other congenital malformations of pancreas and pancreatic duct |
Q600 | CC | 1092:8 codes | Renal agenesis, unilateral |
Q601 | CC | 1092:8 codes | Renal agenesis, bilateral |
Q602 | CC | 1092:8 codes | Renal agenesis, unspecified |
Q603 | CC | 1092:8 codes | Renal hypoplasia, unilateral |
Q604 | CC | 1092:8 codes | Renal hypoplasia, bilateral |
Q605 | CC | 1092:8 codes | Renal hypoplasia, unspecified |
Q606 | CC | 1092:8 codes | Potter's syndrome |
Q6100 | CC | 1093:3 codes | Congenital renal cyst, unspecified |
Q6101 | CC | 1094:2 codes | Congenital single renal cyst |
Q6102 | CC | 1095:4 codes | Congenital multiple renal cysts |
Q6111 | CC | 1096:5 codes | Cystic dilatation of collecting ducts |
Q6119 | CC | 1096:5 codes | Other polycystic kidney, infantile type |
Q612 | CC | 1096:5 codes | Polycystic kidney, adult type |
Q613 | CC | 1096:5 codes | Polycystic kidney, unspecified |
Q614 | CC | 1097:2 codes | Renal dysplasia |
Q615 | CC | 1095:4 codes | Medullary cystic kidney |
Q618 | CC | 1095:4 codes | Other cystic kidney diseases |
Q619 | CC | 1093:3 codes | Cystic kidney disease, unspecified |
Q620 | CC | 1098:7 codes | Congenital hydronephrosis |
Q6210 | CC | 1098:7 codes | Congenital occlusion of ureter, unspecified |
Q6211 | CC | 1098:7 codes | Congenital occlusion of ureteropelvic junction |
Q6212 | CC | 1098:7 codes | Congenital occlusion of ureterovesical orifice |
Q622 | CC | 1098:7 codes | Congenital megaureter |
Q6231 | CC | 3966:8 codes | Congenital ureterocele, orthotopic |
Q6232 | CC | 3968:8 codes | Cecoureterocele |
Q6239 | CC | 1098:7 codes | Other obstructive defects of renal pelvis and ureter |
Q6410 | CC | 1099:7 codes | Exstrophy of urinary bladder, unspecified |
Q6411 | CC | 1099:7 codes | Supravesical fissure of urinary bladder |
Q6412 | CC | 1099:7 codes | Cloacal exstrophy of urinary bladder |
Q6419 | CC | 1099:7 codes | Other exstrophy of urinary bladder |
Q642 | CC | 1100:8 codes | Congenital posterior urethral valves |
Q6431 | CC | 1100:8 codes | Congenital bladder neck obstruction |
Q6432 | CC | 1100:8 codes | Congenital stricture of urethra |
Q6433 | CC | 1100:8 codes | Congenital stricture of urinary meatus |
Q6439 | CC | 1100:8 codes | Other atresia and stenosis of urethra and bladder neck |
Q675 | CC | 1101:7 codes | Congenital deformity of spine |
Q678 | CC | 1102:5 codes | Other congenital deformities of chest |
Q681 | CC | 1102:5 codes | Congenital deformity of finger(s) and hand |
Q743 | CC | 1102:5 codes | Arthrogryposis multiplex congenita |
Q763 | CC | 1101:7 codes | Congenital scoliosis due to congenital bony malformation |
Q76425 | CC | 1101:7 codes | Congenital lordosis, thoracolumbar region |
Q76426 | CC | 1101:7 codes | Congenital lordosis, lumbar region |
Q76427 | CC | 1101:7 codes | Congenital lordosis, lumbosacral region |
Q76428 | CC | 1101:7 codes | Congenital lordosis, sacral and sacrococcygeal region |
Q76429 | CC | 1101:7 codes | Congenital lordosis, unspecified region |
Q766 | CC | 1103:6 codes | Other congenital malformations of ribs |
Q767 | CC | 1103:6 codes | Congenital malformation of sternum |
Q768 | CC | 1103:6 codes | Other congenital malformations of bony thorax |
Q769 | CC | 1103:6 codes | Congenital malformation of bony thorax, unspecified |
Q772 | CC | 1103:6 codes | Short rib syndrome |
Q780 | CC | 1104:10 codes | Osteogenesis imperfecta |
Q782 | CC | 1104:10 codes | Osteopetrosis |
Q790 | MCC | 1105:3 codes | Congenital diaphragmatic hernia |
Q791 | MCC | 1105:3 codes | Other congenital malformations of diaphragm |
Q792 | MCC | 1106:5 codes | Exomphalos |
Q793 | MCC | 1106:5 codes | Gastroschisis |
Q794 | MCC | 1106:5 codes | Prune belly syndrome |
Q7951 | MCC | 1106:5 codes | Congenital hernia of bladder |
Q7959 | MCC | 1106:5 codes | Other congenital malformations of abdominal wall |
Q7960 | CC | 3467:5 codes | Ehlers-Danlos syndrome, unspecified |
Q7961 | CC | 3467:5 codes | Classical Ehlers-Danlos syndrome |
Q7962 | CC | 3467:5 codes | Hypermobile Ehlers-Danlos syndrome |
Q7963 | CC | 3467:5 codes | Vascular Ehlers-Danlos syndrome |
Q7969 | CC | 3467:5 codes | Other Ehlers-Danlos syndromes |
Q851 | CC | 5125:8 codes | Tuberous sclerosis |
Q8581 | CC | 5575:6 codes | PTEN tumor syndrome |
Q8582 | CC | 5572:6 codes | Other Cowden syndrome |
Q8583 | CC | 5570:6 codes | Von Hippel-Lindau syndrome |
Q8589 | CC | 5562:6 codes | Other phakomatoses, not elsewhere classified |
Q859 | CC | 5128:6 codes | Phakomatosis, unspecified |
Q8711 | CC | 2979:2 codes | Prader-Willi syndrome |
Q8719 | CC | 2979:2 codes | Other congenital malformation syndromes predominantly associated with short stature |
Q872 | CC | 6418:18 codes | Congenital malformation syndromes predominantly involving limbs |
Q873 | CC | 6416:18 codes | Congenital malformation syndromes involving early overgrowth |
Q8740 | CC | 6696:27 codes | Marfan syndrome, unspecified |
Q87410 | CC | 6709:27 codes | Marfan syndrome with aortic dilation |
Q87418 | CC | 6713:27 codes | Marfan syndrome with other cardiovascular manifestations |
Q8742 | CC | 6694:27 codes | Marfan syndrome with ocular manifestations |
Q8743 | CC | 6692:27 codes | Marfan syndrome with skeletal manifestation |
Q875 | CC | 6413:24 codes | Other congenital malformation syndromes with other skeletal changes |
Q8781 | CC | 6819:18 codes | Alport syndrome |
Q8782 | CC | 6818:18 codes | Arterial tortuosity syndrome |
Q8783 | CC | 6817:18 codes | Bardet-Biedl syndrome |
Q8784 | CC | 6816:18 codes | Laurence-Moon syndrome |
Q8785 | CC | 6815:18 codes | MED13L syndrome |
Q8789 | CC | 6827:18 codes | Other specified congenital malformation syndromes, not elsewhere classified |
Q8901 | CC | 1111:3 codes | Asplenia (congenital) |
Q8909 | CC | 1111:3 codes | Congenital malformations of spleen |
Q893 | CC | 1112:3 codes | Situs inversus |
Q894 | MCC | 1113:3 codes | Conjoined twins |
Q897 | CC | 1112:3 codes | Multiple congenital malformations, not elsewhere classified |
Q898 | CC | 6447:18 codes | Other specified congenital malformations |
Q910 | CC | 6772:68 codes | Trisomy 18, nonmosaicism (meiotic nondisjunction) |
Q911 | CC | 6780:68 codes | Trisomy 18, mosaicism (mitotic nondisjunction) |
Q912 | CC | 6779:68 codes | Trisomy 18, translocation |
Q913 | CC | 6784:68 codes | Trisomy 18, unspecified |
Q914 | CC | 6783:68 codes | Trisomy 13, nonmosaicism (meiotic nondisjunction) |
Q915 | CC | 6775:68 codes | Trisomy 13, mosaicism (mitotic nondisjunction) |
Q916 | CC | 6774:68 codes | Trisomy 13, translocation |
Q917 | CC | 6776:68 codes | Trisomy 13, unspecified |
Q933 | CC | 3970:61 codes | Deletion of short arm of chromosome 4 |
Q934 | CC | 6798:68 codes | Deletion of short arm of chromosome 5 |
Q9351 | CC | 6497:68 codes | Angelman syndrome |
Q9352 | CC | 6500:68 codes | Phelan-McDermid syndrome |
Q9359 | CC | 6512:68 codes | Other deletions of part of a chromosome |
Q937 | CC | 3972:61 codes | Deletions with other complex rearrangements |
Q9381 | MCC | 6567:68 codes | Velo-cardio-facial syndrome |
Q9382 | CC | 6570:68 codes | Williams syndrome |
Q9388 | CC | 6574:68 codes | Other microdeletions |
Q9389 | CC | 3974:61 codes | Other deletions from the autosomes |
Q939 | CC | 1115:61 codes | Deletion from autosomes, unspecified |
R042 | CC | 1119:6 codes | Hemoptysis |
R0481 | CC | 1119:6 codes | Acute idiopathic pulmonary hemorrhage in infants |
R0489 | CC | 1119:6 codes | Hemorrhage from other sites in respiratory passages |
R049 | CC | 1119:6 codes | Hemorrhage from respiratory passages, unspecified |
R063 | CC | 4894:24 codes | Periodic breathing |
R0901 | CC | 1121:100 codes | Asphyxia |
R092 | MCC | 1121:100 codes | Respiratory arrest |
R17 | CC | 1122:21 codes | Unspecified jaundice |
R180 | CC | 1123:103 codes | Malignant ascites |
R188 | CC | 1123:103 codes | Other ascites |
R290 | CC | 6194:147 codes | Tetany |
R291 | CC | 1125:2 codes | Meningismus |
R295 | CC | 1126:2 codes | Transient paralysis |
R390 | CC | 1127:9 codes | Extravasation of urine |
R4020 | MCC | 4919:880 codes | Unspecified coma |
R402110 | MCC | 5755:878 codes | Coma scale, eyes open, never, unspecified time |
R402111 | MCC | 5756:878 codes | Coma scale, eyes open, never, in the field [EMT or ambulance] |
R402112 | MCC | 5753:878 codes | Coma scale, eyes open, never, at arrival to emergency department |
R402113 | MCC | 5754:878 codes | Coma scale, eyes open, never, at hospital admission |
R402114 | MCC | 5737:878 codes | Coma scale, eyes open, never, 24 hours or more after hospital admission |
R402120 | MCC | 4830:878 codes | Coma scale, eyes open, to pain, unspecified time |
R402121 | MCC | 4826:878 codes | Coma scale, eyes open, to pain, in the field [EMT or ambulance] |
R402122 | MCC | 4828:878 codes | Coma scale, eyes open, to pain, at arrival to emergency department |
R402123 | MCC | 4824:878 codes | Coma scale, eyes open, to pain, at hospital admission |
R402124 | MCC | 4825:878 codes | Coma scale, eyes open, to pain, 24 hours or more after hospital admission |
R402210 | MCC | 5115:878 codes | Coma scale, best verbal response, none, unspecified time |
Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244 01 Mar 2023 06:12:40 CMS, code-revision=344, description-revision=1357 |