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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 1251 of 1375 |
PDX Collection 6595 (continued) | |
R410 | Disorientation, unspecified |
R411 | Anterograde amnesia |
R412 | Retrograde amnesia |
R413 | Other amnesia |
R4182 | Altered mental status, unspecified |
R419 | Unspecified symptoms and signs involving cognitive functions and awareness |
R448 | Other symptoms and signs involving general sensations and perceptions |
R449 | Unspecified symptoms and signs involving general sensations and perceptions |
R4583 | Excessive crying of child, adolescent or adult |
R4584 | Anhedonia |
R460 | Very low level of personal hygiene |
R461 | Bizarre personal appearance |
R462 | Strange and inexplicable behavior |
R463 | Overactivity |
R464 | Slowness and poor responsiveness |
R465 | Suspiciousness and marked evasiveness |
R466 | Undue concern and preoccupation with stressful events |
R467 | Verbosity and circumstantial detail obscuring reason for contact |
R4681 | Obsessive-compulsive behavior |
R4689 | Other symptoms and signs involving appearance and behavior |
R52 | Pain, unspecified |
R570 | Cardiogenic shock |
R571 | Hypovolemic shock |
R578 | Other shock |
R579 | Shock, unspecified |
R6521 | Severe sepsis with septic shock |
R680 | Hypothermia, not associated with low environmental temperature |
R6811 | Excessive crying of infant (baby) |
R6812 | Fussy infant (baby) |
R6813 | Apparent life threatening event in infant (ALTE) |
R6819 | Other nonspecific symptoms peculiar to infancy |
R6881 | Early satiety |
R6882 | Decreased libido |
R6883 | Chills (without fever) |
R6889 | Other general symptoms and signs |
R69 | Illness, unspecified |
PDX Collection 6596 | |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
P2930 | Pulmonary hypertension of newborn |
P2938 | Other persistent fetal circulation |
Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
Q224 | Congenital tricuspid stenosis |
Q225 | Ebstein's anomaly |
Q226 | Hypoplastic right heart syndrome |
Q228 | Other congenital malformations of tricuspid valve |
Q229 | Congenital malformation of tricuspid valve, unspecified |
Q230 | Congenital stenosis of aortic valve |
Q231 | Congenital insufficiency of aortic valve |
Q232 | Congenital mitral stenosis |
Q233 | Congenital mitral insufficiency |
Q234 | Hypoplastic left heart syndrome |
Q238 | Other congenital malformations of aortic and mitral valves |
Q239 | Congenital malformation of aortic and mitral valves, unspecified |
Q248 | Other specified congenital malformations of heart |
Q249 | Congenital malformation of heart, unspecified |
Q2730 | Arteriovenous malformation, site unspecified |
Q274 | Congenital phlebectasia |
Q280 | Arteriovenous malformation of precerebral vessels |
Q281 | Other malformations of precerebral vessels |
Q288 | Other specified congenital malformations of circulatory system |
Q289 | Congenital malformation of circulatory system, unspecified |
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 syndrome, unspecified |
Q87410 | Marfan syndrome with aortic dilation |
Q87418 | Marfan syndrome with other cardiovascular manifestations |
Q8742 | Marfan syndrome with ocular manifestations |
Q8743 | Marfan syndrome with skeletal manifestation |
Q875 | Other congenital malformation syndromes with other skeletal changes |
Q8781 | Alport syndrome |
Q8782 | Arterial tortuosity syndrome |
Q8783 | Bardet-Biedl syndrome |
Q8784 | Laurence-Moon syndrome |
Q8785 | MED13L syndrome |
Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
Q897 | Multiple congenital malformations, not elsewhere classified |
Q898 | Other specified congenital malformations |
Q992 | Fragile X chromosome |
PDX Collection 6597 | |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
P2930 | Pulmonary hypertension of newborn |
P2938 | Other persistent fetal circulation |
Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
Q224 | Congenital tricuspid stenosis |
Q225 | Ebstein's anomaly |
Q226 | Hypoplastic right heart syndrome |
Q228 | Other congenital malformations of tricuspid valve |
Q229 | Congenital malformation of tricuspid valve, unspecified |
Q230 | Congenital stenosis of aortic valve |
Q231 | Congenital insufficiency of aortic valve |
Q232 | Congenital mitral stenosis |
Q233 | Congenital mitral insufficiency |
Q234 | Hypoplastic left heart syndrome |
Q238 | Other congenital malformations of aortic and mitral valves |
Q239 | Congenital malformation of aortic and mitral valves, unspecified |
Q248 | Other specified congenital malformations of heart |
Q249 | Congenital malformation of heart, unspecified |
Q2730 | Arteriovenous malformation, site unspecified |
Q274 | Congenital phlebectasia |
Q280 | Arteriovenous malformation of precerebral vessels |
Q281 | Other malformations of precerebral vessels |
Q288 | Other specified congenital malformations of circulatory system |
Q289 | Congenital malformation of circulatory system, unspecified |
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 syndrome, unspecified |
Q87410 | Marfan syndrome with aortic dilation |
Q87418 | Marfan syndrome with other cardiovascular manifestations |
Q8742 | Marfan syndrome with ocular manifestations |
Q8743 | Marfan syndrome with skeletal manifestation |
Q875 | Other congenital malformation syndromes with other skeletal changes |
Q8781 | Alport syndrome |
Q8782 | Arterial tortuosity syndrome |
Q8783 | Bardet-Biedl syndrome |
Q8784 | Laurence-Moon syndrome |
Q8785 | MED13L syndrome |
Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
Q897 | Multiple congenital malformations, not elsewhere classified |
Q898 | Other specified congenital malformations |
Q992 | Fragile X chromosome |
PDX Collection 6598 | |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
P2930 | Pulmonary hypertension of newborn |
P2938 | Other persistent fetal circulation |
Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
Q224 | Congenital tricuspid stenosis |
Q225 | Ebstein's anomaly |
Q226 | Hypoplastic right heart syndrome |
Q228 | Other congenital malformations of tricuspid valve |
Q229 | Congenital malformation of tricuspid valve, unspecified |
Q230 | Congenital stenosis of aortic valve |
Q231 | Congenital insufficiency of aortic valve |
Q232 | Congenital mitral stenosis |
Q233 | Congenital mitral insufficiency |
Q234 | Hypoplastic left heart syndrome |
Q238 | Other congenital malformations of aortic and mitral valves |
Q239 | Congenital malformation of aortic and mitral valves, unspecified |
Q248 | Other specified congenital malformations of heart |
Q249 | Congenital malformation of heart, unspecified |
Q2730 | Arteriovenous malformation, site unspecified |
Q274 | Congenital phlebectasia |
Q280 | Arteriovenous malformation of precerebral vessels |
Q281 | Other malformations of precerebral vessels |
Q288 | Other specified congenital malformations of circulatory system |
Q289 | Congenital malformation of circulatory system, unspecified |
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 syndrome, unspecified |
Q87410 | Marfan syndrome with aortic dilation |
Q87418 | Marfan syndrome with other cardiovascular manifestations |
Q8742 | Marfan syndrome with ocular manifestations |
Q8743 | Marfan syndrome with skeletal manifestation |
Q875 | Other congenital malformation syndromes with other skeletal changes |
Q8781 | Alport syndrome |
Q8782 | Arterial tortuosity syndrome |
Q8783 | Bardet-Biedl syndrome |
Q8784 | Laurence-Moon syndrome |
Q8785 | MED13L syndrome |
Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
Q897 | Multiple congenital malformations, not elsewhere classified |
Q898 | Other specified congenital malformations |
Q992 | Fragile X chromosome |
PDX Collection 6599 | |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
Q220 | Pulmonary valve atresia |
Q221 | Congenital pulmonary valve stenosis |
Q222 | Congenital pulmonary valve insufficiency |
Q223 | Other congenital malformations of pulmonary valve |
Q238 | Other congenital malformations of aortic and mitral valves |
Q239 | Congenital malformation of aortic and mitral valves, unspecified |
Q248 | Other specified congenital malformations of heart |
Q249 | Congenital malformation of heart, unspecified |
Q2730 | Arteriovenous malformation, site unspecified |
Q274 | Congenital phlebectasia |
Q280 | Arteriovenous malformation of precerebral vessels |
Q281 | Other malformations of precerebral vessels |
Q288 | Other specified congenital malformations of circulatory system |
Q289 | Congenital malformation of circulatory system, unspecified |
Q872 | Congenital malformation syndromes predominantly involving limbs |
Q873 | Congenital malformation syndromes involving early overgrowth |
Q875 | Other congenital malformation syndromes with other skeletal changes |
Q8781 | Alport syndrome |
Q8782 | Arterial tortuosity syndrome |
Q8783 | Bardet-Biedl syndrome |
Q8784 | Laurence-Moon syndrome |
Q8785 | MED13L syndrome |
Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
Q897 | Multiple congenital malformations, not elsewhere classified |
Q898 | Other specified congenital malformations |
PDX Collection 6600 | |
E0840 | Diabetes mellitus due to underlying condition with diabetic neuropathy, unspecified |
E0841 | Diabetes mellitus due to underlying condition with diabetic mononeuropathy |
E0842 | Diabetes mellitus due to underlying condition with diabetic polyneuropathy |
E0843 | Diabetes mellitus due to underlying condition with diabetic autonomic (poly)neuropathy |
E0844 | Diabetes mellitus due to underlying condition with diabetic amyotrophy |
E0849 | Diabetes mellitus due to underlying condition with other diabetic neurological complication |
E0940 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic neuropathy, unspecified |
E0941 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic mononeuropathy |
E0942 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic polyneuropathy |
E0943 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic autonomic (poly)neuropathy |
E0944 | Drug or chemical induced diabetes mellitus with neurological complications with diabetic amyotrophy |
E0949 | Drug or chemical induced diabetes mellitus with neurological complications with other diabetic neurological complication |
E1040 | Type 1 diabetes mellitus with diabetic neuropathy, unspecified |
E1041 | Type 1 diabetes mellitus with diabetic mononeuropathy |
E1042 | Type 1 diabetes mellitus with diabetic polyneuropathy |
E1043 | Type 1 diabetes mellitus with diabetic autonomic (poly)neuropathy |
E1044 | Type 1 diabetes mellitus with diabetic amyotrophy |
E1049 | Type 1 diabetes mellitus with other diabetic neurological complication |
E1140 | Type 2 diabetes mellitus with diabetic neuropathy, unspecified |
E1141 | Type 2 diabetes mellitus with diabetic mononeuropathy |
E1142 | Type 2 diabetes mellitus with diabetic polyneuropathy |
E1143 | Type 2 diabetes mellitus with diabetic autonomic (poly)neuropathy |
E1144 | Type 2 diabetes mellitus with diabetic amyotrophy |
E1149 | Type 2 diabetes mellitus with other diabetic neurological complication |
E1340 | Other specified diabetes mellitus with diabetic neuropathy, unspecified |
E1341 | Other specified diabetes mellitus with diabetic mononeuropathy |
E1342 | Other specified diabetes mellitus with diabetic polyneuropathy |
E1343 | Other specified diabetes mellitus with diabetic autonomic (poly)neuropathy |
E1344 | Other specified diabetes mellitus with diabetic amyotrophy |
E1349 | Other specified diabetes mellitus with other diabetic neurological complication |
G3289 | Other specified degenerative disorders of nervous system in diseases classified elsewhere |
G40001 | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, with status epilepticus |
G40009 | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, without status epilepticus |
G40011 | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, with status epilepticus |
G40019 | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, without status epilepticus |
G40101 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, with status epilepticus |
G40109 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, without status epilepticus |
G40111 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, with status epilepticus |
G40119 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, without status epilepticus |
G40201 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, with status epilepticus |
G40209 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, without status epilepticus |
G40211 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, with status epilepticus |
G40219 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, without status epilepticus |
G40301 | Generalized idiopathic epilepsy and epileptic syndromes, not intractable, with status epilepticus |
G40309 | Generalized idiopathic epilepsy and epileptic syndromes, not intractable, without status epilepticus |
G40311 | Generalized idiopathic epilepsy and epileptic syndromes, intractable, with status epilepticus |
G40319 | Generalized idiopathic epilepsy and epileptic syndromes, intractable, without status epilepticus |
G40401 | Other generalized epilepsy and epileptic syndromes, not intractable, with status epilepticus |
G40409 | Other generalized epilepsy and epileptic syndromes, not intractable, without status epilepticus |
G40411 | Other generalized epilepsy and epileptic syndromes, intractable, with status epilepticus |
G40419 | Other generalized epilepsy and epileptic syndromes, intractable, without status epilepticus |
G4042 | Cyclin-Dependent Kinase-Like 5 Deficiency Disorder |
G40501 | Epileptic seizures related to external causes, not intractable, with status epilepticus |
G40509 | Epileptic seizures related to external causes, not intractable, without status epilepticus |
G40801 | Other epilepsy, not intractable, with status epilepticus |
G40802 | Other epilepsy, not intractable, without status epilepticus |
G40803 | Other epilepsy, intractable, with status epilepticus |
G40804 | Other epilepsy, intractable, without status epilepticus |
G40811 | Lennox-Gastaut syndrome, not intractable, with status epilepticus |
G40812 | Lennox-Gastaut syndrome, not intractable, without status epilepticus |
G40813 | Lennox-Gastaut syndrome, intractable, with status epilepticus |
G40814 | Lennox-Gastaut syndrome, intractable, without status epilepticus |
G40821 | Epileptic spasms, not intractable, with status epilepticus |
G40822 | Epileptic spasms, not intractable, without status epilepticus |
G40823 | Epileptic spasms, intractable, with status epilepticus |
G40824 | Epileptic spasms, intractable, without status epilepticus |
G40833 | Dravet syndrome, intractable, with status epilepticus |
G40834 | Dravet syndrome, intractable, without status epilepticus |
G4089 | Other seizures |
G40901 | Epilepsy, unspecified, not intractable, with status epilepticus |
G40909 | Epilepsy, unspecified, not intractable, without status epilepticus |
G40911 | Epilepsy, unspecified, intractable, with status epilepticus |
G40919 | Epilepsy, unspecified, intractable, without status epilepticus |
G40A01 | Absence epileptic syndrome, not intractable, with status epilepticus |
G40A09 | Absence epileptic syndrome, not intractable, without status epilepticus |
G40A11 | Absence epileptic syndrome, intractable, with status epilepticus |
G40A19 | Absence epileptic syndrome, intractable, without status epilepticus |
G40B01 | Juvenile myoclonic epilepsy, not intractable, with status epilepticus |
G40B09 | Juvenile myoclonic epilepsy, not intractable, without status epilepticus |
G40B11 | Juvenile myoclonic epilepsy, intractable, with status epilepticus |
G40B19 | Juvenile myoclonic epilepsy, intractable, without status epilepticus |
G40C01 | Lafora progressive myoclonus epilepsy, not intractable, with status epilepticus |
G40C09 | Lafora progressive myoclonus epilepsy, not intractable, without status epilepticus |
G40C11 | Lafora progressive myoclonus epilepsy, intractable, with status epilepticus |
G40C19 | Lafora progressive myoclonus epilepsy, intractable, without status epilepticus |
G9381 | Temporal sclerosis |
G9389 | Other specified disorders of brain |
G939 | Disorder of brain, unspecified |
G969 | Disorder of central nervous system, unspecified |
G980 | Neurogenic arthritis, not elsewhere classified |
G988 | Other disorders of nervous system |
G998 | Other specified disorders of nervous system in diseases classified elsewhere |
R561 | Post traumatic seizures |
PDX Collection 6601 | |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
P2930 | Pulmonary hypertension of newborn |
P2938 | Other persistent fetal circulation |
Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
Q220 | Pulmonary valve atresia |
Q221 | Congenital pulmonary valve stenosis |
Q222 | Congenital pulmonary valve insufficiency |
Q223 | Other congenital malformations of pulmonary valve |
Q238 | Other congenital malformations of aortic and mitral valves |
Q239 | Congenital malformation of aortic and mitral valves, unspecified |
Q248 | Other specified congenital malformations of heart |
Q249 | Congenital malformation of heart, unspecified |
Q2730 | Arteriovenous malformation, site unspecified |
Q274 | Congenital phlebectasia |
Q280 | Arteriovenous malformation of precerebral vessels |
Q281 | Other malformations of precerebral vessels |
Q288 | Other specified congenital malformations of circulatory system |
Q289 | Congenital malformation of circulatory system, unspecified |
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 syndrome, unspecified |
Q87410 | Marfan syndrome with aortic dilation |
Q87418 | Marfan syndrome with other cardiovascular manifestations |
Q8742 | Marfan syndrome with ocular manifestations |
Q8743 | Marfan syndrome with skeletal manifestation |
Q875 | Other congenital malformation syndromes with other skeletal changes |
Q8781 | Alport syndrome |
Q8782 | Arterial tortuosity syndrome |
Q8783 | Bardet-Biedl syndrome |
Q8784 | Laurence-Moon syndrome |
Q8785 | MED13L syndrome |
Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
Q897 | Multiple congenital malformations, not elsewhere classified |
Q898 | Other specified congenital malformations |
Q992 | Fragile X chromosome |
PDX Collection 6602 | |
K3189 | Other diseases of stomach and duodenum |
K319 | Disease of stomach and duodenum, unspecified |
K35200 | Acute appendicitis with generalized peritonitis, without perforation or abscess |
K35201 | Acute appendicitis with generalized peritonitis, with perforation, without abscess |
K35209 | Acute appendicitis with generalized peritonitis, without abscess, unspecified as to perforation |
K35210 | Acute appendicitis with generalized peritonitis, without perforation, with abscess |
K35211 | Acute appendicitis with generalized peritonitis, with perforation and abscess |
K35219 | Acute appendicitis with generalized peritonitis, with abscess, unspecified as to perforation |
K3530 | Acute appendicitis with localized peritonitis, without perforation or gangrene |
K3531 | Acute appendicitis with localized peritonitis and gangrene, without perforation |
K3532 | Acute appendicitis with perforation, localized peritonitis, and gangrene, without abscess |
K3533 | Acute appendicitis with perforation, localized peritonitis, and gangrene, with abscess |
K3580 | Unspecified acute appendicitis |
K35890 | Other acute appendicitis without perforation or gangrene |
K35891 | Other acute appendicitis without perforation, with gangrene |
K36 | Other appendicitis |
K37 | Unspecified appendicitis |
K380 | Hyperplasia of appendix |
K381 | Appendicular concretions |
K382 | Diverticulum of appendix |
K383 | Fistula of appendix |
K388 | Other specified diseases of appendix |
K389 | Disease of appendix, unspecified |
K9281 | Gastrointestinal mucositis (ulcerative) |
PDX Collection 6603 | |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
P2930 | Pulmonary hypertension of newborn |
P2938 | Other persistent fetal circulation |
Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
Q224 | Congenital tricuspid stenosis |
Q225 | Ebstein's anomaly |
Q226 | Hypoplastic right heart syndrome |
Q228 | Other congenital malformations of tricuspid valve |
Q229 | Congenital malformation of tricuspid valve, unspecified |
Q230 | Congenital stenosis of aortic valve |
Q231 | Congenital insufficiency of aortic valve |
Q232 | Congenital mitral stenosis |
Q233 | Congenital mitral insufficiency |
Q234 | Hypoplastic left heart syndrome |
Q238 | Other congenital malformations of aortic and mitral valves |
Q239 | Congenital malformation of aortic and mitral valves, unspecified |
Q248 | Other specified congenital malformations of heart |
Q249 | Congenital malformation of heart, unspecified |
Q2730 | Arteriovenous malformation, site unspecified |
Q274 | Congenital phlebectasia |
Q280 | Arteriovenous malformation of precerebral vessels |
Q281 | Other malformations of precerebral vessels |
Q288 | Other specified congenital malformations of circulatory system |
Q289 | Congenital malformation of circulatory system, unspecified |
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 syndrome, unspecified |
Q87410 | Marfan syndrome with aortic dilation |
Q87418 | Marfan syndrome with other cardiovascular manifestations |
Q8742 | Marfan syndrome with ocular manifestations |
Q8743 | Marfan syndrome with skeletal manifestation |
Q875 | Other congenital malformation syndromes with other skeletal changes |
Q8781 | Alport syndrome |
Q8782 | Arterial tortuosity syndrome |
Q8783 | Bardet-Biedl syndrome |
Q8784 | Laurence-Moon syndrome |
Q8785 | MED13L syndrome |
Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
Q897 | Multiple congenital malformations, not elsewhere classified |
Q898 | Other specified congenital malformations |
Q992 | Fragile X chromosome |
PDX Collection 6604 | |
K3189 | Other diseases of stomach and duodenum |
K319 | Disease of stomach and duodenum, unspecified |
K35200 | Acute appendicitis with generalized peritonitis, without perforation or abscess |
K35201 | Acute appendicitis with generalized peritonitis, with perforation, without abscess |
K35209 | Acute appendicitis with generalized peritonitis, without abscess, unspecified as to perforation |
K35210 | Acute appendicitis with generalized peritonitis, without perforation, with abscess |
Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244 01 Mar 2023 06:12:40 CMS, code-revision=344, description-revision=1357 |