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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 1161 of 1375 |
PDX Collection 6207 (continued) | |
N1339 | Other hydronephrosis |
N136 | Pyonephrosis |
N140 | Analgesic nephropathy |
N1411 | Contrast-induced nephropathy |
N1419 | Nephropathy induced by other drugs, medicaments and biological substances |
N142 | Nephropathy induced by unspecified drug, medicament or biological substance |
N143 | Nephropathy induced by heavy metals |
N144 | Toxic nephropathy, not elsewhere classified |
N150 | Balkan nephropathy |
N151 | Renal and perinephric abscess |
N158 | Other specified renal tubulo-interstitial diseases |
N159 | Renal tubulo-interstitial disease, unspecified |
N16 | Renal tubulo-interstitial disorders in diseases classified elsewhere |
N170 | Acute kidney failure with tubular necrosis |
N171 | Acute kidney failure with acute cortical necrosis |
N172 | Acute kidney failure with medullary necrosis |
N178 | Other acute kidney failure |
N179 | Acute kidney failure, unspecified |
N181 | Chronic kidney disease, stage 1 |
N182 | Chronic kidney disease, stage 2 (mild) |
N1832 | Chronic kidney disease, stage 3b |
N184 | Chronic kidney disease, stage 4 (severe) |
N185 | Chronic kidney disease, stage 5 |
N186 | End stage renal disease |
N189 | Chronic kidney disease, unspecified |
N19 | Unspecified kidney failure |
N250 | Renal osteodystrophy |
N251 | Nephrogenic diabetes insipidus |
N2581 | Secondary hyperparathyroidism of renal origin |
N2589 | Other disorders resulting from impaired renal tubular function |
N259 | Disorder resulting from impaired renal tubular function, unspecified |
N261 | Atrophy of kidney (terminal) |
N269 | Renal sclerosis, unspecified |
N270 | Small kidney, unilateral |
N271 | Small kidney, bilateral |
N279 | Small kidney, unspecified |
N281 | Cyst of kidney, acquired |
N2881 | Hypertrophy of kidney |
N2882 | Megaloureter |
N2883 | Nephroptosis |
N2884 | Pyelitis cystica |
N2885 | Pyeloureteritis cystica |
N2886 | Ureteritis cystica |
N2889 | Other specified disorders of kidney and ureter |
N289 | Disorder of kidney and ureter, unspecified |
N29 | Other disorders of kidney and ureter in diseases classified elsewhere |
N3641 | Hypermobility of urethra |
N3642 | Intrinsic sphincter deficiency (ISD) |
N3643 | Combined hypermobility of urethra and intrinsic sphincter deficiency |
N368 | Other specified disorders of urethra |
N369 | Urethral disorder, unspecified |
N390 | Urinary tract infection, site not specified |
N398 | Other specified disorders of urinary system |
N399 | Disorder of urinary system, unspecified |
N80A0 | Endometriosis of bladder, unspecified depth |
N80A1 | Superficial endometriosis of bladder |
N80A2 | Deep endometriosis of bladder |
N80A41 | Superficial endometriosis of right ureter |
N80A42 | Superficial endometriosis of left ureter |
N80A43 | Superficial endometriosis of bilateral ureters |
N80A49 | Superficial endometriosis of unspecified ureter |
N80A51 | Deep endometriosis of right ureter |
N80A52 | Deep endometriosis of left ureter |
N80A53 | Deep endometriosis of bilateral ureters |
N80A59 | Deep endometriosis of unspecified ureter |
N80A61 | Endometriosis of right ureter, unspecified depth |
N80A62 | Endometriosis of left ureter, unspecified depth |
N80A63 | Endometriosis of bilateral ureters, unspecified depth |
N80A69 | Endometriosis of unspecified ureter, unspecified depth |
R310 | Gross hematuria |
R311 | Benign essential microscopic hematuria |
R3121 | Asymptomatic microscopic hematuria |
R3129 | Other microscopic hematuria |
R319 | Hematuria, unspecified |
R8271 | Bacteriuria |
PDX Collection 6208 | |
G041 | Tropical spastic paraplegia |
G10 | Huntington's disease |
G1222 | Progressive bulbar palsy |
G20A1 | Parkinson's disease without dyskinesia, without mention of fluctuations |
G20A2 | Parkinson's disease without dyskinesia, with fluctuations |
G20B1 | Parkinson's disease with dyskinesia, without mention of fluctuations |
G20B2 | Parkinson's disease with dyskinesia, with fluctuations |
G20C | Parkinsonism, unspecified |
G210 | Malignant neuroleptic syndrome |
G2111 | Neuroleptic induced parkinsonism |
G2119 | Other drug induced secondary parkinsonism |
G212 | Secondary parkinsonism due to other external agents |
G213 | Postencephalitic parkinsonism |
G214 | Vascular parkinsonism |
G218 | Other secondary parkinsonism |
G219 | Secondary parkinsonism, unspecified |
G2401 | Drug induced subacute dyskinesia |
G2402 | Drug induced acute dystonia |
G2409 | Other drug induced dystonia |
G241 | Genetic torsion dystonia |
G242 | Idiopathic nonfamilial dystonia |
G243 | Spasmodic torticollis |
G244 | Idiopathic orofacial dystonia |
G245 | Blepharospasm |
G248 | Other dystonia |
G249 | Dystonia, unspecified |
G250 | Essential tremor |
G251 | Drug-induced tremor |
G252 | Other specified forms of tremor |
G253 | Myoclonus |
G254 | Drug-induced chorea |
G255 | Other chorea |
G2561 | Drug induced tics |
G2569 | Other tics of organic origin |
G2570 | Drug induced movement disorder, unspecified |
G2571 | Drug induced akathisia |
G2579 | Other drug induced movement disorders |
G2582 | Stiff-man syndrome |
G2583 | Benign shuddering attacks |
G2589 | Other specified extrapyramidal and movement disorders |
G259 | Extrapyramidal and movement disorder, unspecified |
G26 | Extrapyramidal and movement disorders 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 |
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 |
G803 | Athetoid cerebral palsy |
G804 | Ataxic cerebral palsy |
G808 | Other cerebral palsy |
G809 | Cerebral palsy, unspecified |
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 |
G9200 | Immune effector cell-associated neurotoxicity syndrome, grade unspecified |
G9201 | Immune effector cell-associated neurotoxicity syndrome, grade 1 |
G9202 | Immune effector cell-associated neurotoxicity syndrome, grade 2 |
G9203 | Immune effector cell-associated neurotoxicity syndrome, grade 3 |
G9204 | Immune effector cell-associated neurotoxicity syndrome, grade 4 |
G9205 | Immune effector cell-associated neurotoxicity syndrome, grade 5 |
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 |
G935 | Compression of brain |
G936 | Cerebral edema |
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 |
I6783 | Posterior reversible encephalopathy syndrome |
R532 | Functional quadriplegia |
PDX Collection 6209 | |
I440 | Atrioventricular block, first degree |
I441 | Atrioventricular block, second degree |
I442 | Atrioventricular block, complete |
I4430 | Unspecified atrioventricular block |
I4439 | Other atrioventricular block |
I444 | Left anterior fascicular block |
I445 | Left posterior fascicular block |
I4460 | Unspecified fascicular block |
I4469 | Other fascicular block |
I447 | Left bundle-branch block, unspecified |
I450 | Right fascicular block |
I4510 | Unspecified right bundle-branch block |
I4519 | Other right bundle-branch block |
I452 | Bifascicular block |
I453 | Trifascicular block |
I454 | Nonspecific intraventricular block |
I455 | Other specified heart block |
I456 | Pre-excitation syndrome |
I4581 | Long QT syndrome |
I4589 | Other specified conduction disorders |
I459 | Conduction disorder, unspecified |
I462 | Cardiac arrest due to underlying cardiac condition |
I468 | Cardiac arrest due to other underlying condition |
I469 | Cardiac arrest, cause unspecified |
I470 | Re-entry ventricular arrhythmia |
I4710 | Supraventricular tachycardia, unspecified |
I4711 | Inappropriate sinus tachycardia, so stated |
I4719 | Other supraventricular tachycardia |
I4720 | Ventricular tachycardia, unspecified |
I4721 | Torsades de pointes |
I4729 | Other ventricular tachycardia |
I479 | Paroxysmal tachycardia, unspecified |
I480 | Paroxysmal atrial fibrillation |
I4811 | Longstanding persistent atrial fibrillation |
I4819 | Other persistent atrial fibrillation |
I4820 | Chronic atrial fibrillation, unspecified |
I4821 | Permanent atrial fibrillation |
I483 | Typical atrial flutter |
I484 | Atypical atrial flutter |
I4891 | Unspecified atrial fibrillation |
I4892 | Unspecified atrial flutter |
I4901 | Ventricular fibrillation |
I4902 | Ventricular flutter |
I492 | Junctional premature depolarization |
I498 | Other specified cardiac arrhythmias |
I878 | Other specified disorders of veins |
I879 | Disorder of vein, unspecified |
I998 | Other disorder of circulatory system |
I999 | Unspecified disorder of circulatory system |
R001 | Bradycardia, unspecified |
PDX Collection 6210 | |
D800 | Hereditary hypogammaglobulinemia |
D803 | Selective deficiency of immunoglobulin G [IgG] subclasses |
D804 | Selective deficiency of immunoglobulin M [IgM] |
D805 | Immunodeficiency with increased immunoglobulin M [IgM] |
D806 | Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia |
D807 | Transient hypogammaglobulinemia of infancy |
D808 | Other immunodeficiencies with predominantly antibody defects |
D809 | Immunodeficiency with predominantly antibody defects, unspecified |
D810 | Severe combined immunodeficiency [SCID] with reticular dysgenesis |
D811 | Severe combined immunodeficiency [SCID] with low T- and B-cell numbers |
D812 | Severe combined immunodeficiency [SCID] with low or normal B-cell numbers |
D814 | Nezelof's syndrome |
D816 | Major histocompatibility complex class I deficiency |
D817 | Major histocompatibility complex class II deficiency |
D8182 | Activated Phosphoinositide 3-kinase Delta Syndrome [APDS] |
D8189 | Other combined immunodeficiencies |
D819 | Combined immunodeficiency, unspecified |
D820 | Wiskott-Aldrich syndrome |
D821 | Di George's syndrome |
D822 | Immunodeficiency with short-limbed stature |
D823 | Immunodeficiency following hereditary defective response to Epstein-Barr virus |
D824 | Hyperimmunoglobulin E [IgE] syndrome |
D828 | Immunodeficiency associated with other specified major defects |
D829 | Immunodeficiency associated with major defect, unspecified |
D830 | Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function |
D831 | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders |
D832 | Common variable immunodeficiency with autoantibodies to B- or T-cells |
D838 | Other common variable immunodeficiencies |
D839 | Common variable immunodeficiency, unspecified |
D840 | Lymphocyte function antigen-1 [LFA-1] defect |
D8481 | Immunodeficiency due to conditions classified elsewhere |
D84821 | Immunodeficiency due to drugs |
D84822 | Immunodeficiency due to external causes |
D8489 | Other immunodeficiencies |
D849 | Immunodeficiency, unspecified |
D893 | Immune reconstitution syndrome |
D8940 | Mast cell activation, unspecified |
D8941 | Monoclonal mast cell activation syndrome |
D8942 | Idiopathic mast cell activation syndrome |
D8943 | Secondary mast cell activation |
D8949 | Other mast cell activation disorder |
D8982 | Autoimmune lymphoproliferative syndrome [ALPS] |
D8984 | IgG4-related disease |
D8989 | Other specified disorders involving the immune mechanism, not elsewhere classified |
D899 | Disorder involving the immune mechanism, unspecified |
PDX Collection 6211 | |
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 6212 | |
D800 | Hereditary hypogammaglobulinemia |
D803 | Selective deficiency of immunoglobulin G [IgG] subclasses |
D804 | Selective deficiency of immunoglobulin M [IgM] |
D805 | Immunodeficiency with increased immunoglobulin M [IgM] |
D806 | Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia |
D807 | Transient hypogammaglobulinemia of infancy |
D808 | Other immunodeficiencies with predominantly antibody defects |
D809 | Immunodeficiency with predominantly antibody defects, unspecified |
D810 | Severe combined immunodeficiency [SCID] with reticular dysgenesis |
D811 | Severe combined immunodeficiency [SCID] with low T- and B-cell numbers |
D812 | Severe combined immunodeficiency [SCID] with low or normal B-cell numbers |
D814 | Nezelof's syndrome |
D816 | Major histocompatibility complex class I deficiency |
D817 | Major histocompatibility complex class II deficiency |
D8182 | Activated Phosphoinositide 3-kinase Delta Syndrome [APDS] |
D8189 | Other combined immunodeficiencies |
D819 | Combined immunodeficiency, unspecified |
D820 | Wiskott-Aldrich syndrome |
D821 | Di George's syndrome |
D822 | Immunodeficiency with short-limbed stature |
D823 | Immunodeficiency following hereditary defective response to Epstein-Barr virus |
D824 | Hyperimmunoglobulin E [IgE] syndrome |
D828 | Immunodeficiency associated with other specified major defects |
D829 | Immunodeficiency associated with major defect, unspecified |
D830 | Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function |
D831 | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders |
D832 | Common variable immunodeficiency with autoantibodies to B- or T-cells |
D838 | Other common variable immunodeficiencies |
D839 | Common variable immunodeficiency, unspecified |
D840 | Lymphocyte function antigen-1 [LFA-1] defect |
D8481 | Immunodeficiency due to conditions classified elsewhere |
D84821 | Immunodeficiency due to drugs |
D84822 | Immunodeficiency due to external causes |
D8489 | Other immunodeficiencies |
D849 | Immunodeficiency, unspecified |
D893 | Immune reconstitution syndrome |
D8940 | Mast cell activation, unspecified |
D8941 | Monoclonal mast cell activation syndrome |
D8942 | Idiopathic mast cell activation syndrome |
D8943 | Secondary mast cell activation |
D8949 | Other mast cell activation disorder |
D8982 | Autoimmune lymphoproliferative syndrome [ALPS] |
D8984 | IgG4-related disease |
Centers for Medicare & Medicaid Services, 7500 Security Boulevard Baltimore, MD 21244 01 Mar 2023 06:12:40 CMS, code-revision=344, description-revision=1357 |