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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 1163 of 1375 |
PDX Collection 6222 (continued) | |
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 6223 | |
D800 | Hereditary hypogammaglobulinemia |
D801 | Nonfamilial hypogammaglobulinemia |
D802 | Selective deficiency of immunoglobulin A [IgA] |
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 6224 | |
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 6225 | |
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 6226 | |
I200 | Unstable angina |
I201 | Angina pectoris with documented spasm |
I202 | Refractory angina pectoris |
I2081 | Angina pectoris with coronary microvascular dysfunction |
I2089 | Other forms of angina pectoris |
I209 | Angina pectoris, unspecified |
I2101 | ST elevation (STEMI) myocardial infarction involving left main coronary artery |
I2102 | ST elevation (STEMI) myocardial infarction involving left anterior descending coronary artery |
I2109 | ST elevation (STEMI) myocardial infarction involving other coronary artery of anterior wall |
I2111 | ST elevation (STEMI) myocardial infarction involving right coronary artery |
I2119 | ST elevation (STEMI) myocardial infarction involving other coronary artery of inferior wall |
I2121 | ST elevation (STEMI) myocardial infarction involving left circumflex coronary artery |
I2129 | ST elevation (STEMI) myocardial infarction involving other sites |
I213 | ST elevation (STEMI) myocardial infarction of unspecified site |
I214 | Non-ST elevation (NSTEMI) myocardial infarction |
I219 | Acute myocardial infarction, unspecified |
I21A1 | Myocardial infarction type 2 |
I21A9 | Other myocardial infarction type |
I21B | Myocardial infarction with coronary microvascular dysfunction |
I220 | Subsequent ST elevation (STEMI) myocardial infarction of anterior wall |
I221 | Subsequent ST elevation (STEMI) myocardial infarction of inferior wall |
I222 | Subsequent non-ST elevation (NSTEMI) myocardial infarction |
I228 | Subsequent ST elevation (STEMI) myocardial infarction of other sites |
I229 | Subsequent ST elevation (STEMI) myocardial infarction of unspecified site |
I240 | Acute coronary thrombosis not resulting in myocardial infarction |
I241 | Dressler's syndrome |
I2481 | Acute coronary microvascular dysfunction |
I2489 | Other forms of acute ischemic heart disease |
I249 | Acute ischemic heart disease, unspecified |
I255 | Ischemic cardiomyopathy |
I256 | Silent myocardial ischemia |
I25702 | Atherosclerosis of coronary artery bypass graft(s), unspecified, with refractory angina pectoris |
I25712 | Atherosclerosis of autologous vein coronary artery bypass graft(s) with refractory angina pectoris |
I25722 | Atherosclerosis of autologous artery coronary artery bypass graft(s) with refractory angina pectoris |
I25732 | Atherosclerosis of nonautologous biological coronary artery bypass graft(s) with refractory angina pectoris |
I25752 | Atherosclerosis of native coronary artery of transplanted heart with refractory angina pectoris |
I25762 | Atherosclerosis of bypass graft of coronary artery of transplanted heart with refractory angina pectoris |
I25792 | Atherosclerosis of other coronary artery bypass graft(s) with refractory angina pectoris |
I2585 | Chronic coronary microvascular dysfunction |
I2589 | Other forms of chronic ischemic heart disease |
I259 | Chronic ischemic heart disease, unspecified |
I878 | Other specified disorders of veins |
I879 | Disorder of vein, unspecified |
I998 | Other disorder of circulatory system |
I999 | Unspecified disorder of circulatory system |
PDX Collection 6227 | |
A179 | Tuberculosis of nervous system, unspecified |
A1810 | Tuberculosis of genitourinary system, unspecified |
A1811 | Tuberculosis of kidney and ureter |
A1813 | Tuberculosis of other urinary organs |
A1882 | Tuberculosis of other endocrine glands |
A1884 | Tuberculosis of heart |
A1889 | Tuberculosis of other sites |
A5421 | Gonococcal infection of kidney and ureter |
A5429 | Other gonococcal genitourinary infections |
A5482 | Gonococcal brain abscess |
A5484 | Gonococcal pneumonia |
A5489 | Other gonococcal infections |
A549 | Gonococcal infection, unspecified |
A5900 | Urogenital trichomoniasis, unspecified |
A598 | Trichomoniasis of other sites |
A599 | Trichomoniasis, unspecified |
B3741 | Candidal cystitis and urethritis |
B3742 | Candidal balanitis |
B3749 | Other urogenital candidiasis |
E0821 | Diabetes mellitus due to underlying condition with diabetic nephropathy |
E0822 | Diabetes mellitus due to underlying condition with diabetic chronic kidney disease |
E0829 | Diabetes mellitus due to underlying condition with other diabetic kidney complication |
E0921 | Drug or chemical induced diabetes mellitus with diabetic nephropathy |
E0922 | Drug or chemical induced diabetes mellitus with diabetic chronic kidney disease |
E0929 | Drug or chemical induced diabetes mellitus with other diabetic kidney complication |
M1030 | Gout due to renal impairment, unspecified site |
M10311 | Gout due to renal impairment, right shoulder |
M10312 | Gout due to renal impairment, left shoulder |
M10319 | Gout due to renal impairment, unspecified shoulder |
M10321 | Gout due to renal impairment, right elbow |
M10322 | Gout due to renal impairment, left elbow |
M10329 | Gout due to renal impairment, unspecified elbow |
M10331 | Gout due to renal impairment, right wrist |
M10332 | Gout due to renal impairment, left wrist |
M10339 | Gout due to renal impairment, unspecified wrist |
M10341 | Gout due to renal impairment, right hand |
M10342 | Gout due to renal impairment, left hand |
M10349 | Gout due to renal impairment, unspecified hand |
M10351 | Gout due to renal impairment, right hip |
M10352 | Gout due to renal impairment, left hip |
M10359 | Gout due to renal impairment, unspecified hip |
M10361 | Gout due to renal impairment, right knee |
M10362 | Gout due to renal impairment, left knee |
M10369 | Gout due to renal impairment, unspecified knee |
M10371 | Gout due to renal impairment, right ankle and foot |
M10372 | Gout due to renal impairment, left ankle and foot |
M10379 | Gout due to renal impairment, unspecified ankle and foot |
M1038 | Gout due to renal impairment, vertebrae |
M1039 | Gout due to renal impairment, multiple sites |
N000 | Acute nephritic syndrome with minor glomerular abnormality |
N001 | Acute nephritic syndrome with focal and segmental glomerular lesions |
N002 | Acute nephritic syndrome with diffuse membranous glomerulonephritis |
N003 | Acute nephritic syndrome with diffuse mesangial proliferative glomerulonephritis |
N004 | Acute nephritic syndrome with diffuse endocapillary proliferative glomerulonephritis |
N005 | Acute nephritic syndrome with diffuse mesangiocapillary glomerulonephritis |
N006 | Acute nephritic syndrome with dense deposit disease |
N007 | Acute nephritic syndrome with diffuse crescentic glomerulonephritis |
N008 | Acute nephritic syndrome with other morphologic changes |
N009 | Acute nephritic syndrome with unspecified morphologic changes |
N010 | Rapidly progressive nephritic syndrome with minor glomerular abnormality |
N011 | Rapidly progressive nephritic syndrome with focal and segmental glomerular lesions |
N012 | Rapidly progressive nephritic syndrome with diffuse membranous glomerulonephritis |
N013 | Rapidly progressive nephritic syndrome with diffuse mesangial proliferative glomerulonephritis |
N014 | Rapidly progressive nephritic syndrome with diffuse endocapillary proliferative glomerulonephritis |
N015 | Rapidly progressive nephritic syndrome with diffuse mesangiocapillary glomerulonephritis |
N016 | Rapidly progressive nephritic syndrome with dense deposit disease |
N017 | Rapidly progressive nephritic syndrome with diffuse crescentic glomerulonephritis |
N018 | Rapidly progressive nephritic syndrome with other morphologic changes |
N019 | Rapidly progressive nephritic syndrome with unspecified morphologic changes |
N020 | Recurrent and persistent hematuria with minor glomerular abnormality |
N021 | Recurrent and persistent hematuria with focal and segmental glomerular lesions |
N022 | Recurrent and persistent hematuria with diffuse membranous glomerulonephritis |
N023 | Recurrent and persistent hematuria with diffuse mesangial proliferative glomerulonephritis |
N024 | Recurrent and persistent hematuria with diffuse endocapillary proliferative glomerulonephritis |
N025 | Recurrent and persistent hematuria with diffuse mesangiocapillary glomerulonephritis |
N026 | Recurrent and persistent hematuria with dense deposit disease |
N027 | Recurrent and persistent hematuria with diffuse crescentic glomerulonephritis |
N028 | Recurrent and persistent hematuria with other morphologic changes |
N029 | Recurrent and persistent hematuria with unspecified morphologic changes |
N02B1 | Recurrent and persistent immunoglobulin A nephropathy with glomerular lesion |
N02B2 | Recurrent and persistent immunoglobulin A nephropathy with focal and segmental glomerular lesion |
N02B3 | Recurrent and persistent immunoglobulin A nephropathy with diffuse membranoproliferative glomerulonephritis |
N02B4 | Recurrent and persistent immunoglobulin A nephropathy with diffuse membranous glomerulonephritis |
N02B5 | Recurrent and persistent immunoglobulin A nephropathy with diffuse mesangial proliferative glomerulonephritis |
N02B6 | Recurrent and persistent immunoglobulin A nephropathy with diffuse mesangiocapillary glomerulonephritis |
N02B9 | Other recurrent and persistent immunoglobulin A nephropathy |
N030 | Chronic nephritic syndrome with minor glomerular abnormality |
N031 | Chronic nephritic syndrome with focal and segmental glomerular lesions |
N032 | Chronic nephritic syndrome with diffuse membranous glomerulonephritis |
N033 | Chronic nephritic syndrome with diffuse mesangial proliferative glomerulonephritis |
N034 | Chronic nephritic syndrome with diffuse endocapillary proliferative glomerulonephritis |
N035 | Chronic nephritic syndrome with diffuse mesangiocapillary glomerulonephritis |
N036 | Chronic nephritic syndrome with dense deposit disease |
N037 | Chronic nephritic syndrome with diffuse crescentic glomerulonephritis |
N038 | Chronic nephritic syndrome with other morphologic changes |
N039 | Chronic nephritic syndrome with unspecified morphologic changes |
N040 | Nephrotic syndrome with minor glomerular abnormality |
N041 | Nephrotic syndrome with focal and segmental glomerular lesions |
N0420 | Nephrotic syndrome with diffuse membranous glomerulonephritis, unspecified |
N0421 | Primary membranous nephropathy with nephrotic syndrome |
N0422 | Seconday membranous nephropathy with nephrotic syndrome |
N0429 | Other nephrotic syndrome with diffuse membranous glomerulonephritis |
N043 | Nephrotic syndrome with diffuse mesangial proliferative glomerulonephritis |
N044 | Nephrotic syndrome with diffuse endocapillary proliferative glomerulonephritis |
N045 | Nephrotic syndrome with diffuse mesangiocapillary glomerulonephritis |
N046 | Nephrotic syndrome with dense deposit disease |
N047 | Nephrotic syndrome with diffuse crescentic glomerulonephritis |
N048 | Nephrotic syndrome with other morphologic changes |
N049 | Nephrotic syndrome with unspecified morphologic changes |
N050 | Unspecified nephritic syndrome with minor glomerular abnormality |
N051 | Unspecified nephritic syndrome with focal and segmental glomerular lesions |
N052 | Unspecified nephritic syndrome with diffuse membranous glomerulonephritis |
N053 | Unspecified nephritic syndrome with diffuse mesangial proliferative glomerulonephritis |
N054 | Unspecified nephritic syndrome with diffuse endocapillary proliferative glomerulonephritis |
N055 | Unspecified nephritic syndrome with diffuse mesangiocapillary glomerulonephritis |
N056 | Unspecified nephritic syndrome with dense deposit disease |
N057 | Unspecified nephritic syndrome with diffuse crescentic glomerulonephritis |
N058 | Unspecified nephritic syndrome with other morphologic changes |
N059 | Unspecified nephritic syndrome with unspecified morphologic changes |
N060 | Isolated proteinuria with minor glomerular abnormality |
N061 | Isolated proteinuria with focal and segmental glomerular lesions |
N0620 | Isolated proteinuria with diffuse membranous glomerulonephritis, unspecified |
N0621 | Primary membranous nephropathy with isolated proteinuria |
N0622 | Seconday membranous nephropathy with isolated proteinuria |
N0629 | Other isolated proteinuria with diffuse membranous glomerulonephritis |
N063 | Isolated proteinuria with diffuse mesangial proliferative glomerulonephritis |
N064 | Isolated proteinuria with diffuse endocapillary proliferative glomerulonephritis |
N065 | Isolated proteinuria with diffuse mesangiocapillary glomerulonephritis |
N066 | Isolated proteinuria with dense deposit disease |
N067 | Isolated proteinuria with diffuse crescentic glomerulonephritis |
N068 | Isolated proteinuria with other morphologic lesion |
N069 | Isolated proteinuria with unspecified morphologic lesion |
N070 | Hereditary nephropathy, not elsewhere classified with minor glomerular abnormality |
N071 | Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesions |
N072 | Hereditary nephropathy, not elsewhere classified with diffuse membranous glomerulonephritis |
N073 | Hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritis |
N074 | Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritis |
N075 | Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis |
N076 | Hereditary nephropathy, not elsewhere classified with dense deposit disease |
N077 | Hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritis |
N078 | Hereditary nephropathy, not elsewhere classified with other morphologic lesions |
N079 | Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesions |
N08 | Glomerular disorders in diseases classified elsewhere |
N10 | Acute pyelonephritis |
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