|
Dx Code |
Description |
Dx Code |
Description |
|
700 |
Acquired
Renal Disease |
161 |
IgM
Nephropathy |
|
311 |
Acute
Pyelonephritis |
L901 |
Incidental
Tumor, FL-HCC |
|
L106 |
AHN,
Delta |
L900 |
Incidental
Tumor, Hepatoma |
|
L100 |
AHN,
Drug, Specify |
L902 |
Incidental
Tumor, Mixed CH-HCC |
|
L107 |
AHN,
HAV |
L904 |
Incidental
Tumor, Other, Specify |
|
L102 |
AHN,
HBsAg+ |
L903 |
Incidental
Tumor, Unknown |
|
L108 |
AHN,
HCV |
260 |
Infarction |
|
L109 |
AHN,
HEV |
320 |
Interstitial
Nephritis |
|
L110 |
AHN,
Indeterminate |
801 |
Juvenile
Nephronophthisis |
|
L105 |
AHN,
Other, Specify |
541 |
K-Light
Chain Glomerulosclerosis |
|
421 |
Alport's
Syndrome |
905 |
Light
Chain Nephropathy |
|
L906 |
Amyloidosis,
FAP |
610 |
Lupus
Nephritis (SLE) |
|
L908 |
Amyloidosis,
Primary |
13 |
Malignant
Hypertension |
|
L909 |
Amyloidosis,
Secondary |
440 |
Medullary
Cystic Disease |
|
L910 |
Amyloidosis,
Unknown |
321 |
Medullary
Sponge Kidney Disease |
|
324 |
Analgesic
Abuse Nephropathy |
120 |
Membranoprolif
GN (Mesangcap, Chrhypocompl, LOB, MixMemb) |
|
630 |
Anti-Glomerular
Basement Membrane |
110 |
Membranous
GN |
|
210 |
Arterionephrosclerosis |
611 |
Membranous
Lupus Nephritis |
|
212 |
Atheroembolic
Disease |
612 |
Mesangiopathic
Lupus Nephritis |
|
312 |
Bacterial
Gram Positive Pyelonephritis |
332 |
Mesangio-Proliferative
GN |
|
L600 |
Benign
Tumor, Adenoma |
L400 |
MetDis,
A-1-A |
|
L601 |
Benign
Tumor, Focal Nodular Hyperplasia |
L403 |
MetDis,
GSD - I |
|
L604 |
Benign
Tumor, Lymphoangiomatosis |
L404 |
MetDis,
GSD - IV |
|
L605 |
Benign
Tumor, Other, Specify |
L402 |
MetDis,
Hemochromatosis |
|
L607 |
Benign
Tumor, Polycycstic Disease With Renal |
L405 |
MetDis,
Hyperlipidemia - II |
|
L608 |
Benign
Tumor, Polycycstic Disease W/O Renal |
L406 |
MetDis,
Neurovisceral Storage |
|
L603 |
Benign
Tumor, Pseudoinflammatory Tumor |
L409 |
MetDis,
Other, Specify |
|
L312 |
Biliary
Atresia, Alagille, Kasai |
L407 |
MetDis,
Tyrosinemia |
|
L313 |
Biliary
Atresia, Alagille, No Kasai |
L401 |
MetDis,
Wilson's |
|
L314 |
Biliary
Atresia, Alagille, Unknown |
902 |
Mixed
Connective Tissue Disorder |
|
L306 |
Biliary
Atresia, Extra and Intrahepatic, Kasai |
540 |
Multiple
Myeloma |
|
L316 |
Biliary
Atresia, Extra and Intrahepatic, No Kasai |
907 |
Myoglobinuria |
|
L308 |
Biliary
Atresia, Extra and Intrahepatic, UKN |
340 |
Nephrolithiasis |
|
L300 |
Biliary
Atresia, Extrahepatic, Kasai |
L915 |
Nodular
Regenerative Hyperplasia (NRH) |
|
L301 |
Biliary
Atresia, Extrahepatic, No Kasai |
100 |
Non-Amyloid
Fibrillary Glomerulopathy |
|
L302 |
Biliary
Atresia, Extrahepatic, Unknown |
330 |
Obstructive
Uropathy |
|
L309 |
Biliary
Atresia, Hypoplasia, Kasai |
901 |
Oxalosis |
|
L310 |
Biliary
Atresia, Hypoplasia, No Kasai |
621
|
Polyarteritis
|
|
L311 |
Biliary
Atresia, Hypoplasia, Unknown |
410 |
Polycystic
Kidney Disease |
|
L303 |
Biliary
Atresia, Intrahepatic, Kasai |
L1001 |
Portal
Vein Thrombosis |
|
L304 |
Biliary
Atresia, Intrahepatic, No Kasai |
150 |
Post-Infectious
GN (Acute Bacterial/Viral GN) |
|
L305 |
Biliary
Atresia, Intrahepatic, Unknown |
152 |
Post-Staphylococcal
GN |
|
L315 |
Biliary
Atresia, Unclassified |
151 |
Post-Streptococcal
GN |
|
L1300 |
Biliary
Complications |
153 |
Post-Viral
GN |
|
L501 |
Budd-
Chiari, Polycythemia Vera |
232 |
Pre-Eclalmpsia |
|
L500 |
Budd-Chiari,
Myeloproliferative Disease |
L350 |
Primary
Biliary Cirrhosis (PBC) |
|
L504 |
Budd-Chiari,
Other, Specify |
L1200 |
Primary
Disease Recurrence |
|
L503 |
Budd-Chiari,
Unknown |
L705 |
Primary
Liver Malignancy, Angiosarcoma |
|
L505 |
Budd-Chiari,
Veno Occlusive Disease |
L721 |
Primary
Liver Malignancy, Cholangiocarcinoma (Klatskin) With Sclerosing Cholangitis |
|
180 |
Chronic
GN` |
L722 |
Primary
Liver Malignancy, Cholangiocarcinoma (Klatskin) Without Sclerosing
Cholangitis |
|
I004 |
Chron's
Disease |
L723 |
Primary
Liver Malignancy, Cholangiocarcinoma (Peripheral) With Sclerosing Cholangitis |
|
L210 |
Cirrhosis, HBsAg+ |
L724 |
Primary
Liver Malignancy, Cholangiocarcinoma (Peripheral) Without Sclerosing
Cholangitis |
|
L223 |
Cirrhosis,
Alcoholic With Alcoholic Hep |
L704 |
Primary
Liver Malignancy, Epitheloid Hemangiendothelioma |
|
L224 |
Cirrhosis,
Alcoholic W/O Alcoholic Hep |
L701 |
Primary
Liver Malignancy, FL-HCC |
|
L212 |
Cirrhosis,
Autoimmune, Specify |
L706 |
Primary
Liver Malignancy, Hepatoblastoma (HBL) |
|
L200 |
Cirrhosis,
Cryptogenic |
L700 |
Primary
Liver Malignancy, Hepatoma (HCC) |
|
L222 |
Cirrhosis,
Delta |
L703 |
Primary
Liver Malignancy, Mixed CH-HCC |
|
L221 |
Cirrhosis,
HCV |
L707 |
Primary
Liver Malignancy, Other, Specify |
|
L225 |
Cirrhosis,
NASH (Non-Alcoholic Steatohepatitis) |
L1100 |
Primary
Non-Function (includes poorly functioning graft) |
|
L213 |
Cirrhosis,
Postnecrotic, Drug, Specify |
L361 |
Primary
Sclerosing Cholangitis, Crohn's Disease |
|
L214 |
Cirrhosis,
Postnecrotic, Other, Specify |
L363 |
Primary
Sclerosing Cholangitis, No Bowel Disease |
|
131 |
Cirrhotic
GN |
L360 |
Primary
Sclerosing Cholangitis, Ulcerative Colitis |
|
520 |
Coagulation
Disorder |
640 |
Progressive
Systemic Sclerosis (Sclerodema) |
|
600 |
Collagen-Vascular
Disease |
613 |
Proliferative
Lupus Nephritis |
|
450 |
Congenital
Absence (Aplasia) |
900 |
Prune-Belly
Syndrome |
|
460 |
Congenital
Dysplasia |
310 |
Pyelonephritis |
|
L320 |
Congenital
Hepatic Fibrosis |
802 |
Rapidly
Progressive GN (RPGN) |
|
430 |
Congenital
Hypoplasia |
L1401 |
Rejection:
Acute |
|
322 |
Congenital
Reflux Hydronephrosis |
L1402 |
Rejection:
Chronic |
|
250 |
Cortical
Necrosis |
L1400 |
Rejection:
Humoral |
|
650 |
Cryoglobulinemia |
221 |
Renal
Artery Stenosis |
|
903 |
Cyclosporine
Nephrotoxicity |
222 |
Renal
Artery Thrombosis |
|
L330 |
Cystic
Fibrosis |
731 |
Renal
Cell Carcinoma |
|
480 |
Cystinosis |
240 |
Renal
Vein Thrombosis |
|
250.0 |
Diabetes
Uncompl Adult |
220 |
Renovascular
Hypertension |
|
510 |
Diabetic
Nephropathy (Intercap Glomscler, Kimmel-Wilson) |
300 |
Sarcoidosis |
|
170 |
Diffuse
Proliferative GN (Rap Progr, Acute, Crescentic) |
908 |
Schistosomiasis |
|
323 |
Drug
Induced Interstitial Nephritis |
904 |
Scleroderma |
|
231 |
Eagel
Barrett Syndrome |
L342 |
Secondary
Biliary Cirrhosis, Caroli |
|
211 |
Essential
Hypertension |
L343 |
Secondary
Biliary Cirrhosis, Choledochal Cyst |
|
470 |
Fabry's
Disease |
L340 |
Secondary
Biliary Cirrhosis, Iatrogenic |
|
L420 |
Familial
Cholestasis, Byler |
L344 |
Secondary
Biliary Cirrhosis, Other, Specify |
|
L422 |
Familial
Cholestasis, Other |
L341 |
Secondary
Biliary Cirrhosis, Trauma |
|
L421 |
Familial
Cholestasis, Summerskil |
L800 |
Secondary
Hepatic Malignancy, Carcinoid |
|
906 |
FK506
Toxicity |
L802 |
Secondary
Hepatic Malignancy, Gastrinoma |
|
140 |
Focal
Glomerular Sclerosis (FGS) |
L801 |
Secondary
Hepatic Malignancy, Glucagonoma |
|
160 |
Focal
Proliferative GN (Focal GN) |
L804 |
Secondary
Hepatic Malignancy, Insulinoma |
|
142 |
Focal-Global
Sclerosis |
L803 |
Secondary
Hepatic Malignancy, Other, Specify |
|
141 |
Focal-Segmental
GS (FSGS) |
230 |
Sickle
Cell Anemia |
|
143 |
Focal-Segmental
GS, Collapsing Variety |
909 |
Sjogren's
Syndrome |
|
631 |
Goodpasture's
Syndrome |
I002 |
SMA
Thrombosis |
|
341 |
Gout
(Urate) Nephropathy |
I001 |
SMV
Thrombosis |
|
L916 |
Graft
Versus Host Disease (GVHD) |
500 |
Systemic
Diseases |
|
313 |
Granulomatous
Pyelonephritis |
522 |
Thrombocytopenic
Purpura |
|
521 |
Hemolytic-Uremic
Syndrome |
720 |
Toxins |
|
622 |
Henoch-Schonlein
Purpura |
L1700 |
TPN
Liver Failure |
|
L1000 |
Hepatic
Artery Thrombosis |
710 |
Trauma |
|
L050 |
Hepatitis,
Neonatal |
121 |
Type
I (Subendothelial Deposits) Membranoprolif GN |
|
803 |
Hepatorenal
Syndrome |
122 |
Type
II (Dense-Deposit Disease) Membranoprolif GN |
|
420 |
Hereditary
Nephritis |
800 |
Undetermined |
|
400 |
Hereditary-Congenital
Disorders |
333 |
Ureteral
Reflux |
|
162 |
Heroin
Induced GN |
200 |
Vascular
Disorders |
|
331 |
Horseshoe
Kidney |
620 |
Vasculitis |
|
I003 |
Hypercoagulable
State |
I005 |
Volvulus |
|
130 |
IgA
Nephropathy (Berger's Disease) |
623 |
Wegener's
Granulomatosis |