Dx | CC/MCC | Exclusions | Description |
P2841 | CC | 6051:17 codes | Central neonatal apnea of newborn |
P2842 | CC | 6045:17 codes | Obstructive apnea of newborn |
P2843 | CC | 6047:17 codes | Mixed neonatal apnea of newborn |
P2849 | CC | 6039:17 codes | Other apnea of newborn |
P285 | MCC | 4711:78 codes | Respiratory failure of newborn |
P2881 | MCC | 4707:26 codes | Respiratory arrest of newborn |
P2930 | MCC | 3959:12 codes | Pulmonary hypertension of newborn |
P2938 | MCC | 1028:12 codes | Other persistent fetal circulation |
P2981 | MCC | 1029:1 code | Cardiac arrest of newborn |
P350 | CC | 1030:31 codes | Congenital rubella syndrome |
P351 | MCC | 1030:31 codes | Congenital cytomegalovirus infection |
P352 | MCC | 4049:190 codes | Congenital herpesviral [herpes simplex] infection |
P353 | MCC | 4049:190 codes | Congenital viral hepatitis |
P354 | MCC | 4049:190 codes | Congenital Zika virus disease |
P358 | MCC | 4049:190 codes | Other congenital viral diseases |
P359 | MCC | 4049:190 codes | Congenital viral disease, unspecified |
P360 | MCC | 1031:48 codes | Sepsis of newborn due to streptococcus, group B |
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 | 4049:190 codes | Congenital tuberculosis |
P371 | MCC | 0562:188 codes | Congenital toxoplasmosis |
P372 | MCC | 0562:188 codes | Neonatal (disseminated) listeriosis |
P373 | MCC | 0562:188 codes | Congenital falciparum malaria |
P374 | MCC | 0562:188 codes | Other congenital malaria |
P378 | MCC | 0562:188 codes | Other specified congenital infectious and parasitic diseases |
P379 | MCC | 0562:188 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 | 6589:46 codes | Intra-amniotic infection affecting newborn, not elsewhere classified |
P393 | CC | 5331:54 codes | Neonatal urinary tract infection |
P394 | CC | 6593:46 codes | Neonatal skin infection |
P398 | CC | 6638:46 codes | Other specified infections specific to the perinatal period |
P399 | CC | 6636:46 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 | 6832:90 codes | Anemia of prematurity |
P613 | CC | 6836:90 codes | Congenital anemia from fetal blood loss |
P614 | CC | 6835:92 codes | Other congenital anemias, not elsewhere classified |
P615 | MCC | 6837:66 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 | 1048:25 codes | Convulsions of newborn |
P910 | MCC | 1049:13 codes | Neonatal cerebral ischemia |
P911 | MCC | 1049:13 codes | Acquired periventricular cysts of newborn |
P912 | MCC | 1022:49 codes | Neonatal cerebral leukomalacia |
P913 | MCC | 1049:13 codes | Neonatal cerebral irritability |
P914 | MCC | 1049:13 codes | Neonatal cerebral depression |
P915 | MCC | 1049:13 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 hamartoma 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 | 1121:55 codes | Asphyxia |
R092 | MCC | 1121:55 codes | Respiratory arrest |
R17 | CC | 1122:21 codes | Unspecified jaundice |