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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 1215 of 1375 |
PDX Collection 6449 (continued) | |
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 |
G041 | Tropical spastic paraplegia |
G113 | Cerebellar ataxia with defective DNA repair |
G115 | Hypomyelination - hypogonadotropic hypogonadism - hypodontia |
G116 | Leukodystrophy with vanishing white matter disease |
G118 | Other hereditary ataxias |
G119 | Hereditary ataxia, unspecified |
G120 | Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] |
G121 | Other inherited spinal muscular atrophy |
G1220 | Motor neuron disease, unspecified |
G1221 | Amyotrophic lateral sclerosis |
G1222 | Progressive bulbar palsy |
G1223 | Primary lateral sclerosis |
G1224 | Familial motor neuron disease |
G1225 | Progressive spinal muscle atrophy |
G1229 | Other motor neuron disease |
G128 | Other spinal muscular atrophies and related syndromes |
G129 | Spinal muscular atrophy, unspecified |
G320 | Subacute combined degeneration of spinal cord in diseases classified elsewhere |
G3289 | Other specified degenerative disorders of nervous system in diseases classified elsewhere |
G35 | Multiple sclerosis |
G360 | Neuromyelitis optica [Devic] |
G361 | Acute and subacute hemorrhagic leukoencephalitis [Hurst] |
G368 | Other specified acute disseminated demyelination |
G369 | Acute disseminated demyelination, unspecified |
G370 | Diffuse sclerosis of central nervous system |
G371 | Central demyelination of corpus callosum |
G372 | Central pontine myelinolysis |
G373 | Acute transverse myelitis in demyelinating disease of central nervous system |
G375 | Concentric sclerosis [Balo] of central nervous system |
G3781 | Myelin oligodendrocyte glycoprotein antibody disease |
G3789 | Other specified demyelinating diseases of central nervous system |
G379 | Demyelinating disease of central nervous system, unspecified |
G800 | Spastic quadriplegic cerebral palsy |
G801 | Spastic diplegic cerebral palsy |
G802 | Spastic hemiplegic cerebral palsy |
G804 | Ataxic cerebral palsy |
G808 | Other cerebral palsy |
G809 | Cerebral palsy, unspecified |
G8100 | Flaccid hemiplegia affecting unspecified side |
G8101 | Flaccid hemiplegia affecting right dominant side |
G8102 | Flaccid hemiplegia affecting left dominant side |
G8103 | Flaccid hemiplegia affecting right nondominant side |
G8104 | Flaccid hemiplegia affecting left nondominant side |
G8110 | Spastic hemiplegia affecting unspecified side |
G8111 | Spastic hemiplegia affecting right dominant side |
G8112 | Spastic hemiplegia affecting left dominant side |
G8113 | Spastic hemiplegia affecting right nondominant side |
G8114 | Spastic hemiplegia affecting left nondominant side |
G8190 | Hemiplegia, unspecified affecting unspecified side |
G8191 | Hemiplegia, unspecified affecting right dominant side |
G8192 | Hemiplegia, unspecified affecting left dominant side |
G8193 | Hemiplegia, unspecified affecting right nondominant side |
G8194 | Hemiplegia, unspecified affecting left nondominant side |
G8220 | Paraplegia, unspecified |
G8221 | Paraplegia, complete |
G8222 | Paraplegia, incomplete |
G8250 | Quadriplegia, unspecified |
G8251 | Quadriplegia, C1-C4 complete |
G8252 | Quadriplegia, C1-C4 incomplete |
G8253 | Quadriplegia, C5-C7 complete |
G8254 | Quadriplegia, C5-C7 incomplete |
G830 | Diplegia of upper limbs |
G8310 | Monoplegia of lower limb affecting unspecified side |
G8311 | Monoplegia of lower limb affecting right dominant side |
G8312 | Monoplegia of lower limb affecting left dominant side |
G8313 | Monoplegia of lower limb affecting right nondominant side |
G8314 | Monoplegia of lower limb affecting left nondominant side |
G8320 | Monoplegia of upper limb affecting unspecified side |
G8321 | Monoplegia of upper limb affecting right dominant side |
G8322 | Monoplegia of upper limb affecting left dominant side |
G8323 | Monoplegia of upper limb affecting right nondominant side |
G8324 | Monoplegia of upper limb affecting left nondominant side |
G8330 | Monoplegia, unspecified affecting unspecified side |
G8331 | Monoplegia, unspecified affecting right dominant side |
G8332 | Monoplegia, unspecified affecting left dominant side |
G8333 | Monoplegia, unspecified affecting right nondominant side |
G8334 | Monoplegia, unspecified affecting left nondominant side |
G834 | Cauda equina syndrome |
G835 | Locked-in state |
G8381 | Brown-Sequard syndrome |
G8382 | Anterior cord syndrome |
G8383 | Posterior cord syndrome |
G8384 | Todd's paralysis (postepileptic) |
G8389 | Other specified paralytic syndromes |
G839 | Paralytic syndrome, unspecified |
G9001 | Carotid sinus syncope |
G9009 | Other idiopathic peripheral autonomic neuropathy |
G902 | Horner's syndrome |
G904 | Autonomic dysreflexia |
G9050 | Complex regional pain syndrome I, unspecified |
G90511 | Complex regional pain syndrome I of right upper limb |
G90512 | Complex regional pain syndrome I of left upper limb |
G90513 | Complex regional pain syndrome I of upper limb, bilateral |
G90519 | Complex regional pain syndrome I of unspecified upper limb |
G90521 | Complex regional pain syndrome I of right lower limb |
G90522 | Complex regional pain syndrome I of left lower limb |
G90523 | Complex regional pain syndrome I of lower limb, bilateral |
G90529 | Complex regional pain syndrome I of unspecified lower limb |
G9059 | Complex regional pain syndrome I of other specified site |
G908 | Other disorders of autonomic nervous system |
G909 | Disorder of the autonomic nervous system, unspecified |
G90B | LMNB1-related autosomal dominant leukodystrophy |
G931 | Anoxic brain damage, not elsewhere classified |
G9340 | Encephalopathy, unspecified |
G9341 | Metabolic encephalopathy |
G9342 | Megaloencephalic leukoencephalopathy with subcortical cysts |
G9343 | Leukoencephalopathy with calcifications and cysts |
G9344 | Adult-onset leukodystrophy with axonal spheroids |
G9349 | Other encephalopathy |
G950 | Syringomyelia and syringobulbia |
G9511 | Acute infarction of spinal cord (embolic) (nonembolic) |
G9519 | Other vascular myelopathies |
G9520 | Unspecified cord compression |
G9529 | Other cord compression |
G9581 | Conus medullaris syndrome |
G9589 | Other specified diseases of spinal cord |
G959 | Disease of spinal cord, unspecified |
G9612 | Meningeal adhesions (cerebral) (spinal) |
G969 | Disorder of central nervous system, unspecified |
G971 | Other reaction to spinal and lumbar puncture |
G980 | Neurogenic arthritis, not elsewhere classified |
G988 | Other disorders of nervous system |
G990 | Autonomic neuropathy in diseases classified elsewhere |
G992 | Myelopathy in diseases classified elsewhere |
G998 | Other specified disorders of nervous system in diseases classified elsewhere |
I6783 | Posterior reversible encephalopathy syndrome |
R532 | Functional quadriplegia |
PDX Collection 6450 | |
A021 | Salmonella sepsis |
A207 | Septicemic plague |
A227 | Anthrax sepsis |
A267 | Erysipelothrix sepsis |
A327 | Listerial sepsis |
A392 | Acute meningococcemia |
A393 | Chronic meningococcemia |
A394 | Meningococcemia, unspecified |
A400 | Sepsis due to streptococcus, group A |
A401 | Sepsis due to streptococcus, group B |
A408 | Other streptococcal sepsis |
A409 | Streptococcal sepsis, unspecified |
A4101 | Sepsis due to Methicillin susceptible Staphylococcus aureus |
A4102 | Sepsis due to Methicillin resistant Staphylococcus aureus |
A411 | Sepsis due to other specified staphylococcus |
A412 | Sepsis due to unspecified staphylococcus |
A413 | Sepsis due to Hemophilus influenzae |
A414 | Sepsis due to anaerobes |
A4150 | Gram-negative sepsis, unspecified |
A4151 | Sepsis due to Escherichia coli [E. coli] |
A4152 | Sepsis due to Pseudomonas |
A4153 | Sepsis due to Serratia |
A4154 | Sepsis due to Acinetobacter baumannii |
A4159 | Other Gram-negative sepsis |
A4181 | Sepsis due to Enterococcus |
A4189 | Other specified sepsis |
A419 | Sepsis, unspecified organism |
A427 | Actinomycotic sepsis |
A482 | Nonpneumonic Legionnaires' disease [Pontiac fever] |
A483 | Toxic shock syndrome |
A484 | Brazilian purpuric fever |
A488 | Other specified bacterial diseases |
A4901 | Methicillin susceptible Staphylococcus aureus infection, unspecified site |
A4902 | Methicillin resistant Staphylococcus aureus infection, unspecified site |
A491 | Streptococcal infection, unspecified site |
A492 | Hemophilus influenzae infection, unspecified site |
A493 | Mycoplasma infection, unspecified site |
A498 | Other bacterial infections of unspecified site |
A499 | Bacterial infection, unspecified |
A5486 | Gonococcal sepsis |
B007 | Disseminated herpesviral disease |
B377 | Candidal sepsis |
B92 | Sequelae of leprosy |
B942 | Sequelae of viral hepatitis |
B948 | Sequelae of other specified infectious and parasitic diseases |
B949 | Sequelae of unspecified infectious and parasitic disease |
B950 | Streptococcus, group A, as the cause of diseases classified elsewhere |
B951 | Streptococcus, group B, as the cause of diseases classified elsewhere |
B952 | Enterococcus as the cause of diseases classified elsewhere |
B953 | Streptococcus pneumoniae as the cause of diseases classified elsewhere |
B954 | Other streptococcus as the cause of diseases classified elsewhere |
B955 | Unspecified streptococcus as the cause of diseases classified elsewhere |
B9561 | Methicillin susceptible Staphylococcus aureus infection as the cause of diseases classified elsewhere |
B9562 | Methicillin resistant Staphylococcus aureus infection as the cause of diseases classified elsewhere |
B957 | Other staphylococcus as the cause of diseases classified elsewhere |
B958 | Unspecified staphylococcus as the cause of diseases classified elsewhere |
B960 | Mycoplasma pneumoniae [M. pneumoniae] as the cause of diseases classified elsewhere |
B961 | Klebsiella pneumoniae [K. pneumoniae] as the cause of diseases classified elsewhere |
B9620 | Unspecified Escherichia coli [E. coli] as the cause of diseases classified elsewhere |
B9621 | Shiga toxin-producing Escherichia coli [E. coli] [STEC] O157 as the cause of diseases classified elsewhere |
B9622 | Other specified Shiga toxin-producing Escherichia coli [E. coli] [STEC] as the cause of diseases classified elsewhere |
B9623 | Unspecified Shiga toxin-producing Escherichia coli [E. coli] [STEC] as the cause of diseases classified elsewhere |
B9629 | Other Escherichia coli [E. coli] as the cause of diseases classified elsewhere |
B963 | Hemophilus influenzae [H. influenzae] as the cause of diseases classified elsewhere |
B964 | Proteus (mirabilis) (morganii) as the cause of diseases classified elsewhere |
B965 | Pseudomonas (aeruginosa) (mallei) (pseudomallei) as the cause of diseases classified elsewhere |
B966 | Bacteroides fragilis [B. fragilis] as the cause of diseases classified elsewhere |
B967 | Clostridium perfringens [C. perfringens] as the cause of diseases classified elsewhere |
B9681 | Helicobacter pylori [H. pylori] as the cause of diseases classified elsewhere |
B9682 | Vibrio vulnificus as the cause of diseases classified elsewhere |
B9689 | Other specified bacterial agents as the cause of diseases classified elsewhere |
R6510 | Systemic inflammatory response syndrome (SIRS) of non-infectious origin without acute organ dysfunction |
R6511 | Systemic inflammatory response syndrome (SIRS) of non-infectious origin with acute organ dysfunction |
R6520 | Severe sepsis without septic shock |
Z1610 | Resistance to unspecified beta lactam antibiotics |
Z1611 | Resistance to penicillins |
Z1612 | Extended spectrum beta lactamase (ESBL) resistance |
Z1619 | Resistance to other specified beta lactam antibiotics |
Z1620 | Resistance to unspecified antibiotic |
Z1621 | Resistance to vancomycin |
Z1622 | Resistance to vancomycin related antibiotics |
Z1623 | Resistance to quinolones and fluoroquinolones |
Z1624 | Resistance to multiple antibiotics |
Z1629 | Resistance to other single specified antibiotic |
Z1630 | Resistance to unspecified antimicrobial drugs |
Z1631 | Resistance to antiparasitic drug(s) |
Z1632 | Resistance to antifungal drug(s) |
Z1633 | Resistance to antiviral drug(s) |
Z16341 | Resistance to single antimycobacterial drug |
Z16342 | Resistance to multiple antimycobacterial drugs |
Z1635 | Resistance to multiple antimicrobial drugs |
Z1639 | Resistance to other specified antimicrobial drug |
PDX Collection 6451 | |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
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 |
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 6452 | |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
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 |
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 6453 | |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
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 |
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 6454 | |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
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 |
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 6455 | |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
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 |
Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244 01 Mar 2023 06:12:40 CMS, code-revision=344, description-revision=1357 |