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ICD-10-CM/PCS MS-DRG v41.0 Definitions Manual |
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Appendix C: Principal diagnoses which convert CC/MCC to non-CC |
Page 118 of 1375 |
PDX Collection 1048 (continued) | |
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 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 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 |
Q289 | Congenital malformation of circulatory system, unspecified |
PDX Collection 1076 | |
Q2730 | Arteriovenous malformation, site unspecified |
Q274 | Congenital phlebectasia |
Q280 | Arteriovenous malformation of precerebral vessels |
Q281 | Other malformations of precerebral vessels |
Q282 | Arteriovenous malformation of cerebral vessels |
Q283 | Other malformations of cerebral vessels |
Q288 | Other specified congenital malformations of circulatory system |
Q289 | Congenital malformation of circulatory system, unspecified |
PDX Collection 1078 | |
J398 | Other specified diseases of upper respiratory tract |
J45990 | Exercise induced bronchospasm |
J9809 | Other diseases of bronchus, not elsewhere classified |
Q311 | Congenital subglottic stenosis |
Q312 | Laryngeal hypoplasia |
Q313 | Laryngocele |
Q315 | Congenital laryngomalacia |
Q318 | Other congenital malformations of larynx |
Q319 | Congenital malformation of larynx, unspecified |
Q320 | Congenital tracheomalacia |
Q321 | Other congenital malformations of trachea |
Q322 | Congenital bronchomalacia |
Q323 | Congenital stenosis of bronchus |
Q324 | Other congenital malformations of bronchus |
Q340 | Anomaly of pleura |
Q341 | Congenital cyst of mediastinum |
Q348 | Other specified congenital malformations of respiratory system |
Q349 | Congenital malformation of respiratory system, unspecified |
PDX Collection 1079 | |
Q330 | Congenital cystic lung |
Q331 | Accessory lobe of lung |
Q332 | Sequestration of lung |
Q333 | Agenesis of lung |
Q334 | Congenital bronchiectasis |
Q335 | Ectopic tissue in lung |
Q336 | Congenital hypoplasia and dysplasia of lung |
Q338 | Other congenital malformations of lung |
Q339 | Congenital malformation of lung, unspecified |
Q340 | Anomaly of pleura |
Q341 | Congenital cyst of mediastinum |
Q348 | Other specified congenital malformations of respiratory system |
Q349 | Congenital malformation of respiratory system, unspecified |
PDX Collection 1081 | |
Q390 | Atresia of esophagus without fistula |
Q391 | Atresia of esophagus with tracheo-esophageal fistula |
Q392 | Congenital tracheo-esophageal fistula without atresia |
Q393 | Congenital stenosis and stricture of esophagus |
Q394 | Esophageal web |
Q395 | Congenital dilatation of esophagus |
Q396 | Congenital diverticulum of esophagus |
Q398 | Other congenital malformations of esophagus |
Q399 | Congenital malformation of esophagus, unspecified |
Q458 | Other specified congenital malformations of digestive system |
Q459 | Congenital malformation of digestive system, unspecified |
PDX Collection 1082 | |
Q395 | Congenital dilatation of esophagus |
Q396 | Congenital diverticulum of esophagus |
Q398 | Other congenital malformations of esophagus |
Q399 | Congenital malformation of esophagus, unspecified |
Q458 | Other specified congenital malformations of digestive system |
Q459 | Congenital malformation of digestive system, unspecified |
PDX Collection 1083 | |
Q410 | Congenital absence, atresia and stenosis of duodenum |
Q411 | Congenital absence, atresia and stenosis of jejunum |
Q412 | Congenital absence, atresia and stenosis of ileum |
Q418 | Congenital absence, atresia and stenosis of other specified parts of small intestine |
Q419 | Congenital absence, atresia and stenosis of small intestine, part unspecified |
Q458 | Other specified congenital malformations of digestive system |
Q459 | Congenital malformation of digestive system, unspecified |
PDX Collection 1084 | |
Q420 | Congenital absence, atresia and stenosis of rectum with fistula |
Q421 | Congenital absence, atresia and stenosis of rectum without fistula |
Q422 | Congenital absence, atresia and stenosis of anus with fistula |
Q423 | Congenital absence, atresia and stenosis of anus without fistula |
Q428 | Congenital absence, atresia and stenosis of other parts of large intestine |
Q429 | Congenital absence, atresia and stenosis of large intestine, part unspecified |
Q458 | Other specified congenital malformations of digestive system |
Q459 | Congenital malformation of digestive system, unspecified |
PDX Collection 1085 | |
Q431 | Hirschsprung's disease |
Q432 | Other congenital functional disorders of colon |
Q458 | Other specified congenital malformations of digestive system |
Q459 | Congenital malformation of digestive system, unspecified |
PDX Collection 1086 | |
Q433 | Congenital malformations of intestinal fixation |
Q434 | Duplication of intestine |
Q435 | Ectopic anus |
Q436 | Congenital fistula of rectum and anus |
Q437 | Persistent cloaca |
Q438 | Other specified congenital malformations of intestine |
Q439 | Congenital malformation of intestine, unspecified |
PDX Collection 1087 | |
Q410 | Congenital absence, atresia and stenosis of duodenum |
Q411 | Congenital absence, atresia and stenosis of jejunum |
Q412 | Congenital absence, atresia and stenosis of ileum |
Q418 | Congenital absence, atresia and stenosis of other specified parts of small intestine |
Q419 | Congenital absence, atresia and stenosis of small intestine, part unspecified |
Q420 | Congenital absence, atresia and stenosis of rectum with fistula |
Q421 | Congenital absence, atresia and stenosis of rectum without fistula |
Q422 | Congenital absence, atresia and stenosis of anus with fistula |
Q423 | Congenital absence, atresia and stenosis of anus without fistula |
Q428 | Congenital absence, atresia and stenosis of other parts of large intestine |
Q429 | Congenital absence, atresia and stenosis of large intestine, part unspecified |
Q430 | Meckel's diverticulum (displaced) (hypertrophic) |
Q431 | Hirschsprung's disease |
Q432 | Other congenital functional disorders of colon |
Q433 | Congenital malformations of intestinal fixation |
Q434 | Duplication of intestine |
Q435 | Ectopic anus |
Q436 | Congenital fistula of rectum and anus |
Q437 | Persistent cloaca |
Q438 | Other specified congenital malformations of intestine |
Q439 | Congenital malformation of intestine, unspecified |
PDX Collection 1089 | |
Q442 | Atresia of bile ducts |
Q443 | Congenital stenosis and stricture of bile ducts |
Q458 | Other specified congenital malformations of digestive system |
Q459 | Congenital malformation of digestive system, unspecified |
PDX Collection 1091 | |
Q450 | Agenesis, aplasia and hypoplasia of pancreas |
Q451 | Annular pancreas |
Q452 | Congenital pancreatic cyst |
Q453 | Other congenital malformations of pancreas and pancreatic duct |
Q458 | Other specified congenital malformations of digestive system |
Q459 | Congenital malformation of digestive system, unspecified |
PDX Collection 1092 | |
N139 | Obstructive and reflux uropathy, unspecified |
Q600 | Renal agenesis, unilateral |
Q601 | Renal agenesis, bilateral |
Q602 | Renal agenesis, unspecified |
Q603 | Renal hypoplasia, unilateral |
Q604 | Renal hypoplasia, bilateral |
Q605 | Renal hypoplasia, unspecified |
Q606 | Potter's syndrome |
PDX Collection 1093 | |
N139 | Obstructive and reflux uropathy, unspecified |
Q6100 | Congenital renal cyst, unspecified |
Q619 | Cystic kidney disease, unspecified |
PDX Collection 1094 | |
N139 | Obstructive and reflux uropathy, unspecified |
Q6101 | Congenital single renal cyst |
PDX Collection 1095 | |
N139 | Obstructive and reflux uropathy, unspecified |
Q6102 | Congenital multiple renal cysts |
Q615 | Medullary cystic kidney |
Q618 | Other cystic kidney diseases |
PDX Collection 1096 | |
N139 | Obstructive and reflux uropathy, unspecified |
Q6111 | Cystic dilatation of collecting ducts |
Q6119 | Other polycystic kidney, infantile type |
Q612 | Polycystic kidney, adult type |
Q613 | Polycystic kidney, unspecified |
PDX Collection 1097 | |
N139 | Obstructive and reflux uropathy, unspecified |
Q614 | Renal dysplasia |
PDX Collection 1098 | |
N139 | Obstructive and reflux uropathy, unspecified |
Q620 | Congenital hydronephrosis |
Q6210 | Congenital occlusion of ureter, unspecified |
Q6211 | Congenital occlusion of ureteropelvic junction |
Q6212 | Congenital occlusion of ureterovesical orifice |
Q622 | Congenital megaureter |
Q6239 | Other obstructive defects of renal pelvis and ureter |
PDX Collection 1099 | |
N139 | Obstructive and reflux uropathy, unspecified |
Q6410 | Exstrophy of urinary bladder, unspecified |
Q6411 | Supravesical fissure of urinary bladder |
Q6412 | Cloacal exstrophy of urinary bladder |
Q6419 | Other exstrophy of urinary bladder |
Q648 | Other specified congenital malformations of urinary system |
Q649 | Congenital malformation of urinary system, unspecified |
PDX Collection 1100 | |
N139 | Obstructive and reflux uropathy, unspecified |
Q642 | Congenital posterior urethral valves |
Q6431 | Congenital bladder neck obstruction |
Q6432 | Congenital stricture of urethra |
Q6433 | Congenital stricture of urinary meatus |
Q6439 | Other atresia and stenosis of urethra and bladder neck |
Q648 | Other specified congenital malformations of urinary system |
Q649 | Congenital malformation of urinary system, unspecified |
PDX Collection 1101 | |
Q675 | Congenital deformity of spine |
Q763 | Congenital scoliosis due to congenital bony malformation |
Q76425 | Congenital lordosis, thoracolumbar region |
Q76426 | Congenital lordosis, lumbar region |
Q76427 | Congenital lordosis, lumbosacral region |
Q76428 | Congenital lordosis, sacral and sacrococcygeal region |
Q76429 | Congenital lordosis, unspecified region |
PDX Collection 1102 | |
Q676 | Pectus excavatum |
Q677 | Pectus carinatum |
Q678 | Other congenital deformities of chest |
Q681 | Congenital deformity of finger(s) and hand |
Q743 | Arthrogryposis multiplex congenita |
PDX Collection 1103 | |
Q765 | Cervical rib |
Q766 | Other congenital malformations of ribs |
Q767 | Congenital malformation of sternum |
Q768 | Other congenital malformations of bony thorax |
Q769 | Congenital malformation of bony thorax, unspecified |
Q772 | Short rib syndrome |
PDX Collection 1104 | |
Q773 | Chondrodysplasia punctata |
Q776 | Chondroectodermal dysplasia |
Q780 | Osteogenesis imperfecta |
Q781 | Polyostotic fibrous dysplasia |
Q782 | Osteopetrosis |
Q783 | Progressive diaphyseal dysplasia |
Q785 | Metaphyseal dysplasia |
Q786 | Multiple congenital exostoses |
Q788 | Other specified osteochondrodysplasias |
Q789 | Osteochondrodysplasia, unspecified |
PDX Collection 1105 | |
Q401 | Congenital hiatus hernia |
Q790 | Congenital diaphragmatic hernia |
Q791 | Other congenital malformations of diaphragm |
PDX Collection 1106 | |
Q792 | Exomphalos |
Q793 | Gastroschisis |
Q794 | Prune belly syndrome |
Q7951 | Congenital hernia of bladder |
Q7959 | Other congenital malformations of abdominal wall |
PDX Collection 1111 | |
Q8901 | Asplenia (congenital) |
Q8909 | Congenital malformations of spleen |
Q899 | Congenital malformation, unspecified |
PDX Collection 1112 | |
Q893 | Situs inversus |
Q897 | Multiple congenital malformations, not elsewhere classified |
Q899 | Congenital malformation, unspecified |
PDX Collection 1113 | |
Q894 | Conjoined twins |
Q897 | Multiple congenital malformations, not elsewhere classified |
Q899 | Congenital malformation, unspecified |
PDX Collection 1115 | |
Q900 | Trisomy 21, nonmosaicism (meiotic nondisjunction) |
Q901 | Trisomy 21, mosaicism (mitotic nondisjunction) |
Q902 | Trisomy 21, translocation |
Q909 | Down syndrome, unspecified |
Q910 | Trisomy 18, nonmosaicism (meiotic nondisjunction) |
Q911 | Trisomy 18, mosaicism (mitotic nondisjunction) |
Q912 | Trisomy 18, translocation |
Q913 | Trisomy 18, unspecified |
Q914 | Trisomy 13, nonmosaicism (meiotic nondisjunction) |
Q915 | Trisomy 13, mosaicism (mitotic nondisjunction) |
Q916 | Trisomy 13, translocation |
Q917 | Trisomy 13, unspecified |
Q920 | Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction) |
Q921 | Whole chromosome trisomy, mosaicism (mitotic nondisjunction) |
Q922 | Partial trisomy |
Q925 | Duplications with other complex rearrangements |
Q9261 | Marker chromosomes in normal individual |
Q9262 | Marker chromosomes in abnormal individual |
Q927 | Triploidy and polyploidy |
Q928 | Other specified trisomies and partial trisomies of autosomes |
Q929 | Trisomy and partial trisomy of autosomes, unspecified |
Q930 | Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction) |
Q931 | Whole chromosome monosomy, mosaicism (mitotic nondisjunction) |
Q932 | Chromosome replaced with ring, dicentric or isochromosome |
Q934 | Deletion of short arm of chromosome 5 |
Q9381 | Velo-cardio-facial syndrome |
Q9388 | Other microdeletions |
Q939 | Deletion from autosomes, unspecified |
Q950 | Balanced translocation and insertion in normal individual |
Q951 | Chromosome inversion in normal individual |
Q952 | Balanced autosomal rearrangement in abnormal individual |
Q953 | Balanced sex/autosomal rearrangement in abnormal individual |
Q955 | Individual with autosomal fragile site |
Q958 | Other balanced rearrangements and structural markers |
Q959 | Balanced rearrangement and structural marker, unspecified |
Q960 | Karyotype 45, X |
Q961 | Karyotype 46, X iso (Xq) |
Q962 | Karyotype 46, X with abnormal sex chromosome, except iso (Xq) |
Q963 | Mosaicism, 45, X/46, XX or XY |
Q964 | Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome |
Q968 | Other variants of Turner's syndrome |
Q969 | Turner's syndrome, unspecified |
Q970 | Karyotype 47, XXX |
Q971 | Female with more than three X chromosomes |
Q972 | Mosaicism, lines with various numbers of X chromosomes |
Q973 | Female with 46, XY karyotype |
Q978 | Other specified sex chromosome abnormalities, female phenotype |
Q979 | Sex chromosome abnormality, female phenotype, unspecified |
Q980 | Klinefelter syndrome karyotype 47, XXY |
Q981 | Klinefelter syndrome, male with more than two X chromosomes |
Q983 | Other male with 46, XX karyotype |
Q984 | Klinefelter syndrome, unspecified |
Q985 | Karyotype 47, XYY |
Q986 | Male with structurally abnormal sex chromosome |
Q987 | Male with sex chromosome mosaicism |
Q988 | Other specified sex chromosome abnormalities, male phenotype |
Q989 | Sex chromosome abnormality, male phenotype, unspecified |
Q990 | Chimera 46, XX/46, XY |
Q991 | 46, XX true hermaphrodite |
Q998 | Other specified chromosome abnormalities |
Q999 | Chromosomal abnormality, unspecified |
PDX Collection 1119 | |
R042 | Hemoptysis |
R0481 | Acute idiopathic pulmonary hemorrhage in infants |
R0489 | Hemorrhage from other sites in respiratory passages |
R049 | Hemorrhage from respiratory passages, unspecified |
R093 | Abnormal sputum |
R6813 | Apparent life threatening event in infant (ALTE) |
PDX Collection 1121 | |
G890 | Central pain syndrome |
G8911 | Acute pain due to trauma |
G8912 | Acute post-thoracotomy pain |
G8918 | Other acute postprocedural pain |
G8921 | Chronic pain due to trauma |
G8922 | Chronic post-thoracotomy pain |
G8928 | Other chronic postprocedural pain |
G8929 | Other chronic pain |
G893 | Neoplasm related pain (acute) (chronic) |
G894 | Chronic pain syndrome |
J80 | Acute respiratory distress syndrome |
J9600 | Acute respiratory failure, unspecified whether with hypoxia or hypercapnia |
J9601 | Acute respiratory failure with hypoxia |
J9602 | Acute respiratory failure with hypercapnia |
J9610 | Chronic respiratory failure, unspecified whether with hypoxia or hypercapnia |
J9611 | Chronic respiratory failure with hypoxia |
J9612 | Chronic respiratory failure with hypercapnia |
J9620 | Acute and chronic respiratory failure, unspecified whether with hypoxia or hypercapnia |
J9621 | Acute and chronic respiratory failure with hypoxia |
J9622 | Acute and chronic respiratory failure with hypercapnia |
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