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 G: Diagnoses Defined as Complications or Comorbidities |
| Page 15 of 37 |
| A000 B083 C7240 C84Z1 E7200 F3181 H4742 I75023 K51012 L97518 M4858XA M84512P M87032 N983 O98312 S0211HA S12390A S32111A S42036P S42432K S52031K S52256N S52392R S58011A S62222P S62613K S72031K S72331R S72462R S82026P S82201M S82441Q S82873P S92046P S92513K T333XXA T83512A |
| O98312 | Other infections with a predominantly sexual mode of transmission complicating pregnancy, second trimester |
| O98313 | Other infections with a predominantly sexual mode of transmission complicating pregnancy, third trimester |
| O9832 | Other infections with a predominantly sexual mode of transmission complicating childbirth |
| O9833 | Other infections with a predominantly sexual mode of transmission complicating the puerperium |
| O98411 | Viral hepatitis complicating pregnancy, first trimester |
| O98412 | Viral hepatitis complicating pregnancy, second trimester |
| O98413 | Viral hepatitis complicating pregnancy, third trimester |
| O9842 | Viral hepatitis complicating childbirth |
| O9843 | Viral hepatitis complicating the puerperium |
| O98511 | Other viral diseases complicating pregnancy, first trimester |
| O98512 | Other viral diseases complicating pregnancy, second trimester |
| O98513 | Other viral diseases complicating pregnancy, third trimester |
| O9852 | Other viral diseases complicating childbirth |
| O9853 | Other viral diseases complicating the puerperium |
| O98611 | Protozoal diseases complicating pregnancy, first trimester |
| O98612 | Protozoal diseases complicating pregnancy, second trimester |
| O98613 | Protozoal diseases complicating pregnancy, third trimester |
| O9862 | Protozoal diseases complicating childbirth |
| O9863 | Protozoal diseases complicating the puerperium |
| O98711 | Human immunodeficiency virus [HIV] disease complicating pregnancy, first trimester |
| O98712 | Human immunodeficiency virus [HIV] disease complicating pregnancy, second trimester |
| O98713 | Human immunodeficiency virus [HIV] disease complicating pregnancy, third trimester |
| O9872 | Human immunodeficiency virus [HIV] disease complicating childbirth |
| O9873 | Human immunodeficiency virus [HIV] disease complicating the puerperium |
| O98811 | Other maternal infectious and parasitic diseases complicating pregnancy, first trimester |
| O98812 | Other maternal infectious and parasitic diseases complicating pregnancy, second trimester |
| O98813 | Other maternal infectious and parasitic diseases complicating pregnancy, third trimester |
| O9882 | Other maternal infectious and parasitic diseases complicating childbirth |
| O9883 | Other maternal infectious and parasitic diseases complicating the puerperium |
| O98911 | Unspecified maternal infectious and parasitic disease complicating pregnancy, first trimester |
| O98912 | Unspecified maternal infectious and parasitic disease complicating pregnancy, second trimester |
| O98913 | Unspecified maternal infectious and parasitic disease complicating pregnancy, third trimester |
| O9892 | Unspecified maternal infectious and parasitic disease complicating childbirth |
| O9893 | Unspecified maternal infectious and parasitic disease complicating the puerperium |
| O99111 | Other diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism complicating pregnancy, first trimester |
| O99112 | Other diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism complicating pregnancy, second trimester |
| O99113 | Other diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism complicating pregnancy, third trimester |
| O99119 | Other diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism complicating pregnancy, unspecified trimester |
| O9912 | Other diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism complicating childbirth |
| O9913 | Other diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism complicating the puerperium |
| O99321 | Drug use complicating pregnancy, first trimester |
| O99322 | Drug use complicating pregnancy, second trimester |
| O99323 | Drug use complicating pregnancy, third trimester |
| O99324 | Drug use complicating childbirth |
| O99325 | Drug use complicating the puerperium |
| O99354 | Diseases of the nervous system complicating childbirth |
| O99355 | Diseases of the nervous system complicating the puerperium |
| O99411 | Diseases of the circulatory system complicating pregnancy, first trimester |
| O99412 | Diseases of the circulatory system complicating pregnancy, second trimester |
| O99413 | Diseases of the circulatory system complicating pregnancy, third trimester |
| O9943 | Diseases of the circulatory system complicating the puerperium |
| O99830 | Other infection carrier state complicating pregnancy |
| O99834 | Other infection carrier state complicating childbirth |
| O99835 | Other infection carrier state complicating the puerperium |
| P102 | Intraventricular hemorrhage due to birth injury |
| P122 | Epicranial subaponeurotic hemorrhage due to birth injury |
| P280 | Primary atelectasis of newborn |
| P2810 | Unspecified atelectasis of newborn |
| P2811 | Resorption atelectasis without respiratory distress syndrome |
| P2819 | Other atelectasis of newborn |
| P282 | Cyanotic attacks of newborn |
| P2830 | Primary sleep apnea of newborn, unspecified |
| P2831 | Primary central sleep apnea of newborn |
| P2832 | Primary obstructive sleep apnea of newborn |
| P2833 | Primary mixed sleep apnea of newborn |
| P2839 | Other primary sleep apnea of newborn |
| P2840 | Unspecified apnea of newborn |
| P2841 | Central neonatal apnea of newborn |
| P2842 | Obstructive apnea of newborn |
| P2843 | Mixed neonatal apnea of newborn |
| P2849 | Other apnea of newborn |
| P350 | Congenital rubella syndrome |
| P381 | Omphalitis with mild hemorrhage |
| P389 | Omphalitis without hemorrhage |
| P390 | Neonatal infective mastitis |
| P392 | Intra-amniotic infection affecting newborn, not elsewhere classified |
| P393 | Neonatal urinary tract infection |
| P394 | Neonatal skin infection |
| P398 | Other specified infections specific to the perinatal period |
| P399 | Infection specific to the perinatal period, unspecified |
| P520 | Intraventricular (nontraumatic) hemorrhage, grade 1, of newborn |
| P521 | Intraventricular (nontraumatic) hemorrhage, grade 2, of newborn |
| P523 | Unspecified intraventricular (nontraumatic) hemorrhage of newborn |
| P53 | Hemorrhagic disease of newborn |
| P544 | Neonatal adrenal hemorrhage |
| P612 | Anemia of prematurity |
| P613 | Congenital anemia from fetal blood loss |
| P614 | Other congenital anemias, not elsewhere classified |
| P616 | Other transient neonatal disorders of coagulation |
| P702 | Neonatal diabetes mellitus |
| P708 | Other transitory disorders of carbohydrate metabolism of newborn |
| 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 |
| P720 | Neonatal goiter, not elsewhere classified |
| P721 | Transitory neonatal hyperthyroidism |
| P722 | Other transitory neonatal disorders of thyroid function, not elsewhere classified |
| P728 | Other specified transitory neonatal endocrine disorders |
| P7441 | Alkalosis of newborn |
| P745 | Transitory tyrosinemia of newborn |
| P746 | Transitory hyperammonemia of newborn |
| P748 | Other transitory metabolic disturbances of newborn |
| P761 | Transitory ileus of newborn |
| P830 | Sclerema neonatorum |
| P8330 | Unspecified edema specific to newborn |
| P8339 | Other edema specific to newborn |
| P9160 | Hypoxic ischemic encephalopathy [HIE], unspecified |
| P9161 | Mild hypoxic ischemic encephalopathy [HIE] |
| P9162 | Moderate hypoxic ischemic encephalopathy [HIE] |
| P930 | Grey baby syndrome |
| P938 | Other reactions and intoxications due to drugs administered to newborn |
| P940 | Transient neonatal myasthenia gravis |
| P961 | Neonatal withdrawal symptoms from maternal use of drugs of addiction |
| P962 | Withdrawal symptoms from therapeutic use of drugs in newborn |
| Q010 | Frontal encephalocele |
| Q011 | Nasofrontal encephalocele |
| Q012 | Occipital encephalocele |
| Q018 | Encephalocele of other sites |
| Q019 | Encephalocele, unspecified |
| Q044 | Septo-optic dysplasia of brain |
| Q045 | Megalencephaly |
| Q046 | Congenital cerebral cysts |
| Q048 | Other specified congenital malformations of brain |
| Q050 | Cervical spina bifida with hydrocephalus |
| Q051 | Thoracic spina bifida with hydrocephalus |
| Q052 | Lumbar spina bifida with hydrocephalus |
| Q053 | Sacral spina bifida with hydrocephalus |
| Q054 | Unspecified spina bifida with hydrocephalus |
| Q0702 | Arnold-Chiari syndrome with hydrocephalus |
| Q0703 | Arnold-Chiari syndrome with spina bifida and hydrocephalus |
| Q205 | Discordant atrioventricular connection |
| Q210 | Ventricular septal defect |
| Q2110 | Atrial septal defect, unspecified |
| Q2111 | Secundum atrial septal defect |
| Q2112 | Patent foramen ovale |
| Q2113 | Coronary sinus atrial septal defect |
| Q2114 | Superior sinus venosus atrial septal defect |
| Q2115 | Inferior sinus venosus atrial septal defect |
| Q2116 | Sinus venosus atrial septal defect, unspecified |
| Q2119 | Other specified atrial septal defect |
| Q2120 | Atrioventricular septal defect, unspecified as to partial or complete |
| Q2121 | Partial atrioventricular septal defect |
| Q2122 | Transitional atrioventricular septal defect |
| Q2123 | Complete atrioventricular septal defect |
| Q221 | Congenital pulmonary valve stenosis |
| Q222 | Congenital pulmonary valve insufficiency |
| Q223 | Other congenital malformations of pulmonary valve |
| Q230 | Congenital stenosis of aortic valve |
| Q231 | Congenital insufficiency of aortic valve |
| Q232 | Congenital mitral stenosis |
| Q233 | Congenital mitral insufficiency |
| Q240 | Dextrocardia |
| Q241 | Levocardia |
| Q243 | Pulmonary infundibular stenosis |
| Q245 | Malformation of coronary vessels |
| Q250 | Patent ductus arteriosus |
| 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 |
| Q260 | Congenital stenosis of vena cava |
| Q261 | Persistent left superior vena cava |
| Q262 | Total anomalous pulmonary venous connection |
| Q263 | Partial anomalous pulmonary venous connection |
| Q264 | Anomalous pulmonary venous connection, unspecified |
| Q268 | Other congenital malformations of great veins |
| 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 |
| 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 |
| Q330 | Congenital cystic lung |
| Q334 | Congenital bronchiectasis |
| Q395 | Congenital dilatation of esophagus |
| Q396 | Congenital diverticulum of esophagus |
| Q398 | Other congenital malformations of esophagus |
| Q399 | Congenital malformation of esophagus, unspecified |
| 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 |
| 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 |
| Q440 | Agenesis, aplasia and hypoplasia of gallbladder |
| Q441 | Other congenital malformations of gallbladder |
| Q444 | Choledochal cyst |
| Q445 | Other congenital malformations of bile ducts |
| Q446 | Cystic disease of liver |
| Q447 | Other congenital malformations of liver |
| Q450 | Agenesis, aplasia and hypoplasia of pancreas |
| Q451 | Annular pancreas |
| Q452 | Congenital pancreatic cyst |
| Q453 | Other congenital malformations of pancreas and pancreatic duct |
| 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 |
| Q6100 | Congenital renal cyst, unspecified |
| Q6101 | Congenital single renal cyst |
| Q6102 | Congenital multiple renal cysts |
| Q6111 | Cystic dilatation of collecting ducts |
| Q6119 | Other polycystic kidney, infantile type |
| Q612 | Polycystic kidney, adult type |
| Q613 | Polycystic kidney, unspecified |
| Q614 | Renal dysplasia |
| Q615 | Medullary cystic kidney |
| Q618 | Other cystic kidney diseases |
| Q619 | Cystic kidney disease, 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 |
| Q6231 | Congenital ureterocele, orthotopic |
| Q6232 | Cecoureterocele |
| Q6239 | Other obstructive defects of renal pelvis and ureter |
| Q6410 | Exstrophy of urinary bladder, unspecified |
| Q6411 | Supravesical fissure of urinary bladder |
| Q6412 | Cloacal exstrophy of urinary bladder |
| Q6419 | Other exstrophy of urinary bladder |
| 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 |
| Q675 | Congenital deformity of spine |
| Q678 | Other congenital deformities of chest |
| Q681 | Congenital deformity of finger(s) and hand |
| Q743 | Arthrogryposis multiplex congenita |
| 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 |
| 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 |
| Q780 | Osteogenesis imperfecta |
| Q782 | Osteopetrosis |
| Q7960 | Ehlers-Danlos syndrome, unspecified |
| Q7961 | Classical Ehlers-Danlos syndrome |
| Q7962 | Hypermobile Ehlers-Danlos syndrome |
| Q7963 | Vascular Ehlers-Danlos syndrome |
| Q7969 | Other Ehlers-Danlos syndromes |
| Q851 | Tuberous sclerosis |
| Q8581 | PTEN tumor syndrome |
| Q8582 | Other Cowden syndrome |
| Q8583 | Von Hippel-Lindau syndrome |
| Q8589 | Other phakomatoses, not elsewhere classified |
| Q859 | Phakomatosis, unspecified |
| Q8711 | Prader-Willi syndrome |
| Q8719 | Other congenital malformation syndromes predominantly associated with short stature |
| 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 |
| Q8901 | Asplenia (congenital) |
| Q8909 | Congenital malformations of spleen |
| Q893 | Situs inversus |
| Q897 | Multiple congenital malformations, not elsewhere classified |
| Q898 | Other specified congenital malformations |
| 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 |
| Q933 | Deletion of short arm of chromosome 4 |
| Q934 | Deletion of short arm of chromosome 5 |
| Q9351 | Angelman syndrome |
| Q9359 | Other deletions of part of a chromosome |
| Q937 | Deletions with other complex rearrangements |
| Q9382 | Williams syndrome |
| Q9388 | Other microdeletions |
| Q9389 | Other deletions from the autosomes |
| Q939 | Deletion from autosomes, unspecified |
| R042 | Hemoptysis |
| R0481 | Acute idiopathic pulmonary hemorrhage in infants |
| R0489 | Hemorrhage from other sites in respiratory passages |
| R049 | Hemorrhage from respiratory passages, unspecified |
| R063 | Periodic breathing |
| R0901 | Asphyxia |
| R17 | Unspecified jaundice |
| R180 | Malignant ascites |
| R188 | Other ascites |
| R290 | Tetany |
| R291 | Meningismus |
| R295 | Transient paralysis |
| R390 | Extravasation of urine |
| R403 | Persistent vegetative state |
| R414 | Neurologic neglect syndrome |
| R440 | Auditory hallucinations |
| R442 | Other hallucinations |
| R443 | Hallucinations, unspecified |
| R45851 | Suicidal ideations |
| R4701 | Aphasia |
| R5600 | Simple febrile convulsions |
| R5601 | Complex febrile convulsions |
| R561 | Post traumatic seizures |
| R579 | Shock, unspecified |
| R64 | Cachexia |
| R6510 | Systemic inflammatory response syndrome (SIRS) of non-infectious origin without acute organ dysfunction |
| R710 | Precipitous drop in hematocrit |
| R7881 | Bacteremia |
| R820 | Chyluria |
| R821 | Myoglobinuria |
| S01101A | Unspecified open wound of right eyelid and periocular area, initial encounter |
| S01102A | Unspecified open wound of left eyelid and periocular area, initial encounter |
| S01109A | Unspecified open wound of unspecified eyelid and periocular area, initial encounter |
| S020XXA | Fracture of vault of skull, initial encounter for closed fracture |
| S020XXK | Fracture of vault of skull, subsequent encounter for fracture with nonunion |
| S02101A | Fracture of base of skull, right side, initial encounter for closed fracture |
| S02101K | Fracture of base of skull, right side, subsequent encounter for fracture with nonunion |
| S02102A | Fracture of base of skull, left side, initial encounter for closed fracture |
| S02102K | Fracture of base of skull, left side, subsequent encounter for fracture with nonunion |
| S02109A | Fracture of base of skull, unspecified side, initial encounter for closed fracture |
| S02109K | Fracture of base of skull, unspecified side, subsequent encounter for fracture with nonunion |
| S02110A | Type I occipital condyle fracture, unspecified side, initial encounter for closed fracture |
| S02110K | Type I occipital condyle fracture, unspecified side, subsequent encounter for fracture with nonunion |
| S02111A | Type II occipital condyle fracture, unspecified side, initial encounter for closed fracture |
| S02111K | Type II occipital condyle fracture, unspecified side, subsequent encounter for fracture with nonunion |
| S02112A | Type III occipital condyle fracture, unspecified side, initial encounter for closed fracture |
| S02112K | Type III occipital condyle fracture, unspecified side, subsequent encounter for fracture with nonunion |
| S02113A | Unspecified occipital condyle fracture, initial encounter for closed fracture |
| S02113K | Unspecified occipital condyle fracture, subsequent encounter for fracture with nonunion |
| S02118A | Other fracture of occiput, unspecified side, initial encounter for closed fracture |
| S02118K | Other fracture of occiput, unspecified side, subsequent encounter for fracture with nonunion |
| S02119A | Unspecified fracture of occiput, initial encounter for closed fracture |
| S02119K | Unspecified fracture of occiput, subsequent encounter for fracture with nonunion |
| S0211AA | Type I occipital condyle fracture, right side, initial encounter for closed fracture |
| S0211AK | Type I occipital condyle fracture, right side, subsequent encounter for fracture with nonunion |
| S0211BA | Type I occipital condyle fracture, left side, initial encounter for closed fracture |
| S0211BK | Type I occipital condyle fracture, left side, subsequent encounter for fracture with nonunion |
| S0211CA | Type II occipital condyle fracture, right side, initial encounter for closed fracture |
| S0211CK | Type II occipital condyle fracture, right side, subsequent encounter for fracture with nonunion |
| S0211DA | Type II occipital condyle fracture, left side, initial encounter for closed fracture |
| S0211DK | Type II occipital condyle fracture, left side, subsequent encounter for fracture with nonunion |
| S0211EA | Type III occipital condyle fracture, right side, initial encounter for closed fracture |
| S0211EK | Type III occipital condyle fracture, right side, subsequent encounter for fracture with nonunion |
| S0211FA | Type III occipital condyle fracture, left side, initial encounter for closed fracture |
| S0211FK | Type III occipital condyle fracture, left side, subsequent encounter for fracture with nonunion |
| S0211GA | Other fracture of occiput, right side, initial encounter for closed fracture |
| S0211GK | Other fracture of occiput, right side, subsequent encounter for fracture with nonunion |
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Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244 16 Mar 2022 17:08:13 CMS, code-revision=333, description-revision=1331 |