PDX Collection 6917 (continued) |
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 |
N04A | Nephrotic syndrome with C3 glomerulonephritis |
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 |
N05A | Unspecified nephritic syndrome with C3 glomerulonephritis |
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 | Secondary 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 |
N06A | Isolated proteinuria with C3 glomerulonephritis |
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 |
N07A | Hereditary nephropathy, not elsewhere classified with C3 glomerulonephritis |
N118 | Other chronic tubulo-interstitial nephritis |
N119 | Chronic tubulo-interstitial nephritis, unspecified |
N12 | Tubulo-interstitial nephritis, not specified as acute or chronic |
N1411 | Contrast-induced nephropathy |
N1419 | Nephropathy induced by other drugs, medicaments and biological substances |
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 |
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 |
|
PDX Collection 6918 |
D474 | Osteomyelofibrosis |
D500 | Iron deficiency anemia secondary to blood loss (chronic) |
D501 | Sideropenic dysphagia |
D508 | Other iron deficiency anemias |
D509 | Iron deficiency anemia, unspecified |
D510 | Vitamin B12 deficiency anemia due to intrinsic factor deficiency |
D511 | Vitamin B12 deficiency anemia due to selective vitamin B12 malabsorption with proteinuria |
D512 | Transcobalamin II deficiency |
D513 | Other dietary vitamin B12 deficiency anemia |
D518 | Other vitamin B12 deficiency anemias |
D519 | Vitamin B12 deficiency anemia, unspecified |
D520 | Dietary folate deficiency anemia |
D521 | Drug-induced folate deficiency anemia |
D528 | Other folate deficiency anemias |
D529 | Folate deficiency anemia, unspecified |
D530 | Protein deficiency anemia |
D531 | Other megaloblastic anemias, not elsewhere classified |
D532 | Scorbutic anemia |
D538 | Other specified nutritional anemias |
D539 | Nutritional anemia, unspecified |
D550 | Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency |
D551 | Anemia due to other disorders of glutathione metabolism |
D5521 | Anemia due to pyruvate kinase deficiency |
D5529 | Anemia due to other disorders of glycolytic enzymes |
D553 | Anemia due to disorders of nucleotide metabolism |
D558 | Other anemias due to enzyme disorders |
D559 | Anemia due to enzyme disorder, unspecified |
D560 | Alpha thalassemia |
D561 | Beta thalassemia |
D562 | Delta-beta thalassemia |
D563 | Thalassemia minor |
D564 | Hereditary persistence of fetal hemoglobin [HPFH] |
D565 | Hemoglobin E-beta thalassemia |
D568 | Other thalassemias |
D569 | Thalassemia, unspecified |
D5700 | Hb-SS disease with crisis, unspecified |
D5701 | Hb-SS disease with acute chest syndrome |
D5702 | Hb-SS disease with splenic sequestration |
D571 | Sickle-cell disease without crisis |
D5720 | Sickle-cell/Hb-C disease without crisis |
D57211 | Sickle-cell/Hb-C disease with acute chest syndrome |
D57212 | Sickle-cell/Hb-C disease with splenic sequestration |
D57213 | Sickle-cell/Hb-C disease with cerebral vascular involvement |
D57214 | Sickle-cell/Hb-C disease with dactylitis |
D57218 | Sickle-cell/Hb-C disease with crisis with other specified complication |
D57219 | Sickle-cell/Hb-C disease with crisis, unspecified |
D573 | Sickle-cell trait |
D5740 | Sickle-cell thalassemia without crisis |
D57411 | Sickle-cell thalassemia, unspecified, with acute chest syndrome |
D57412 | Sickle-cell thalassemia, unspecified, with splenic sequestration |
D57419 | Sickle-cell thalassemia, unspecified, with crisis |
D5780 | Other sickle-cell disorders without crisis |
D57811 | Other sickle-cell disorders with acute chest syndrome |
D57812 | Other sickle-cell disorders with splenic sequestration |
D57819 | Other sickle-cell disorders with crisis, unspecified |
D580 | Hereditary spherocytosis |
D581 | Hereditary elliptocytosis |
D582 | Other hemoglobinopathies |
D588 | Other specified hereditary hemolytic anemias |
D589 | Hereditary hemolytic anemia, unspecified |
D590 | Drug-induced autoimmune hemolytic anemia |
D5910 | Autoimmune hemolytic anemia, unspecified |
D5911 | Warm autoimmune hemolytic anemia |
D5912 | Cold autoimmune hemolytic anemia |
D5913 | Mixed type autoimmune hemolytic anemia |
D5919 | Other autoimmune hemolytic anemia |
D592 | Drug-induced nonautoimmune hemolytic anemia |
D5930 | Hemolytic-uremic syndrome, unspecified |
D5931 | Infection-associated hemolytic-uremic syndrome |
D5932 | Hereditary hemolytic-uremic syndrome |
D5939 | Other hemolytic-uremic syndrome |
D594 | Other nonautoimmune hemolytic anemias |
D595 | Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli] |
D596 | Hemoglobinuria due to hemolysis from other external causes |
D598 | Other acquired hemolytic anemias |
D599 | Acquired hemolytic anemia, unspecified |
D600 | Chronic acquired pure red cell aplasia |
D601 | Transient acquired pure red cell aplasia |
D608 | Other acquired pure red cell aplasias |
D609 | Acquired pure red cell aplasia, unspecified |
D6101 | Constitutional (pure) red blood cell aplasia |
D6102 | Shwachman-Diamond syndrome |
D6109 | Other constitutional aplastic anemia |
D611 | Drug-induced aplastic anemia |
D612 | Aplastic anemia due to other external agents |
D613 | Idiopathic aplastic anemia |
D61810 | Antineoplastic chemotherapy induced pancytopenia |
D61811 | Other drug-induced pancytopenia |
D61818 | Other pancytopenia |
D6182 | Myelophthisis |
D6189 | Other specified aplastic anemias and other bone marrow failure syndromes |
D619 | Aplastic anemia, unspecified |
D62 | Acute posthemorrhagic anemia |
D640 | Hereditary sideroblastic anemia |
D642 | Secondary sideroblastic anemia due to drugs and toxins |
D643 | Other sideroblastic anemias |
D644 | Congenital dyserythropoietic anemia |
D6481 | Anemia due to antineoplastic chemotherapy |
D6489 | Other specified anemias |
D649 | Anemia, unspecified |
D68312 | Antiphospholipid antibody with hemorrhagic disorder |
D6851 | Activated protein C resistance |
D6852 | Prothrombin gene mutation |
D6859 | Other primary thrombophilia |
D6861 | Antiphospholipid syndrome |
D6862 | Lupus anticoagulant syndrome |
D6869 | Other thrombophilia |
D7589 | Other specified diseases of blood and blood-forming organs |
D759 | Disease of blood and blood-forming organs, unspecified |
D75A | Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia |
D892 | Hypergammaglobulinemia, unspecified |
|
PDX Collection 6919 |
A020 | Salmonella enteritis |
A039 | Shigellosis, unspecified |
A040 | Enteropathogenic Escherichia coli infection |
A041 | Enterotoxigenic Escherichia coli infection |
A042 | Enteroinvasive Escherichia coli infection |
A043 | Enterohemorrhagic Escherichia coli infection |
A044 | Other intestinal Escherichia coli infections |
A045 | Campylobacter enteritis |
A046 | Enteritis due to Yersinia enterocolitica |
A0471 | Enterocolitis due to Clostridium difficile, recurrent |
A0472 | Enterocolitis due to Clostridium difficile, not specified as recurrent |
A048 | Other specified bacterial intestinal infections |
A049 | Bacterial intestinal infection, unspecified |
A050 | Foodborne staphylococcal intoxication |
A052 | Foodborne Clostridium perfringens [Clostridium welchii] intoxication |
A060 | Acute amebic dysentery |
A061 | Chronic intestinal amebiasis |
A062 | Amebic nondysenteric colitis |
A069 | Amebiasis, unspecified |
A071 | Giardiasis [lambliasis] |
A072 | Cryptosporidiosis |
A073 | Isosporiasis |
A074 | Cyclosporiasis |
A078 | Other specified protozoal intestinal diseases |
A079 | Protozoal intestinal disease, unspecified |
A080 | Rotaviral enteritis |
A0811 | Acute gastroenteropathy due to Norwalk agent |
A0819 | Acute gastroenteropathy due to other small round viruses |
A082 | Adenoviral enteritis |
A0831 | Calicivirus enteritis |
A0832 | Astrovirus enteritis |
A0839 | Other viral enteritis |
A084 | Viral intestinal infection, unspecified |
A088 | Other specified intestinal infections |
A09 | Infectious gastroenteritis and colitis, unspecified |
A1832 | Tuberculous enteritis |
A1839 | Retroperitoneal tuberculosis |
A1883 | Tuberculosis of digestive tract organs, not elsewhere classified |
B3782 | Candidal enteritis |
B829 | Intestinal parasitism, unspecified |
J09X3 | Influenza due to identified novel influenza A virus with gastrointestinal manifestations |
J09X9 | Influenza due to identified novel influenza A virus with other manifestations |
J102 | Influenza due to other identified influenza virus with gastrointestinal manifestations |
J1081 | Influenza due to other identified influenza virus with encephalopathy |
J1082 | Influenza due to other identified influenza virus with myocarditis |
J1083 | Influenza due to other identified influenza virus with otitis media |
J1089 | Influenza due to other identified influenza virus with other manifestations |
J112 | Influenza due to unidentified influenza virus with gastrointestinal manifestations |
J1181 | Influenza due to unidentified influenza virus with encephalopathy |
J1182 | Influenza due to unidentified influenza virus with myocarditis |
J1183 | Influenza due to unidentified influenza virus with otitis media |
J1189 | Influenza due to unidentified influenza virus with other manifestations |
K30 | Functional dyspepsia |
K3184 | Gastroparesis |
K521 | Toxic gastroenteritis and colitis |
K5221 | Food protein-induced enterocolitis syndrome |
K5222 | Food protein-induced enteropathy |
K5229 | Other allergic and dietetic gastroenteritis and colitis |
K523 | Indeterminate colitis |
K5282 | Eosinophilic colitis |
K52831 | Collagenous colitis |
K52832 | Lymphocytic colitis |
K52838 | Other microscopic colitis |
K52839 | Microscopic colitis, unspecified |
K5289 | Other specified noninfective gastroenteritis and colitis |
K529 | Noninfective gastroenteritis and colitis, unspecified |
K580 | Irritable bowel syndrome with diarrhea |
K581 | Irritable bowel syndrome with constipation |
K582 | Mixed irritable bowel syndrome |
K588 | Other irritable bowel syndrome |
K589 | Irritable bowel syndrome without diarrhea |
K650 | Generalized (acute) peritonitis |
K652 | Spontaneous bacterial peritonitis |
K658 | Other peritonitis |
K6812 | Psoas muscle abscess |
K6819 | Other retroperitoneal abscess |
K682 | Retroperitoneal fibrosis |
K683 | Retroperitoneal hematoma |
K689 | Other disorders of retroperitoneum |
P768 | Other specified intestinal obstruction of newborn |
P769 | Intestinal obstruction of newborn, unspecified |
P771 | Stage 1 necrotizing enterocolitis in newborn |
P772 | Stage 2 necrotizing enterocolitis in newborn |
P773 | Stage 3 necrotizing enterocolitis in newborn |
P779 | Necrotizing enterocolitis in newborn, unspecified |
P781 | Other neonatal peritonitis |
P783 | Noninfective neonatal diarrhea |
P7881 | Congenital cirrhosis (of liver) |
P7882 | Peptic ulcer of newborn |
P7883 | Newborn esophageal reflux |
P7884 | Gestational alloimmune liver disease |
P7889 | Other specified perinatal digestive system disorders |
|
PDX Collection 6920 |
A020 | Salmonella enteritis |
A039 | Shigellosis, unspecified |
A040 | Enteropathogenic Escherichia coli infection |
A041 | Enterotoxigenic Escherichia coli infection |
A042 | Enteroinvasive Escherichia coli infection |
A043 | Enterohemorrhagic Escherichia coli infection |
A044 | Other intestinal Escherichia coli infections |
A045 | Campylobacter enteritis |
A046 | Enteritis due to Yersinia enterocolitica |
A0471 | Enterocolitis due to Clostridium difficile, recurrent |
A0472 | Enterocolitis due to Clostridium difficile, not specified as recurrent |
A048 | Other specified bacterial intestinal infections |
A049 | Bacterial intestinal infection, unspecified |
A050 | Foodborne staphylococcal intoxication |
A052 | Foodborne Clostridium perfringens [Clostridium welchii] intoxication |
A060 | Acute amebic dysentery |
A061 | Chronic intestinal amebiasis |
A062 | Amebic nondysenteric colitis |
A069 | Amebiasis, unspecified |
A071 | Giardiasis [lambliasis] |
A072 | Cryptosporidiosis |
A073 | Isosporiasis |
A074 | Cyclosporiasis |
A078 | Other specified protozoal intestinal diseases |
A079 | Protozoal intestinal disease, unspecified |
A080 | Rotaviral enteritis |
A0811 | Acute gastroenteropathy due to Norwalk agent |
A0819 | Acute gastroenteropathy due to other small round viruses |
A082 | Adenoviral enteritis |
A0831 | Calicivirus enteritis |
A0832 | Astrovirus enteritis |
A0839 | Other viral enteritis |
A084 | Viral intestinal infection, unspecified |
A088 | Other specified intestinal infections |
A09 | Infectious gastroenteritis and colitis, unspecified |
A1832 | Tuberculous enteritis |
A1839 | Retroperitoneal tuberculosis |
A1883 | Tuberculosis of digestive tract organs, not elsewhere classified |
B3782 | Candidal enteritis |
B829 | Intestinal parasitism, unspecified |
J09X3 | Influenza due to identified novel influenza A virus with gastrointestinal manifestations |
J09X9 | Influenza due to identified novel influenza A virus with other manifestations |
J102 | Influenza due to other identified influenza virus with gastrointestinal manifestations |
J1081 | Influenza due to other identified influenza virus with encephalopathy |
J1082 | Influenza due to other identified influenza virus with myocarditis |
J1083 | Influenza due to other identified influenza virus with otitis media |
J1089 | Influenza due to other identified influenza virus with other manifestations |
J112 | Influenza due to unidentified influenza virus with gastrointestinal manifestations |
J1181 | Influenza due to unidentified influenza virus with encephalopathy |
J1182 | Influenza due to unidentified influenza virus with myocarditis |
J1183 | Influenza due to unidentified influenza virus with otitis media |
J1189 | Influenza due to unidentified influenza virus with other manifestations |
K30 | Functional dyspepsia |
K3184 | Gastroparesis |
K521 | Toxic gastroenteritis and colitis |
K5221 | Food protein-induced enterocolitis syndrome |
K5222 | Food protein-induced enteropathy |
K5229 | Other allergic and dietetic gastroenteritis and colitis |
K523 | Indeterminate colitis |
K5282 | Eosinophilic colitis |
K52831 | Collagenous colitis |
K52832 | Lymphocytic colitis |
K52838 | Other microscopic colitis |
K52839 | Microscopic colitis, unspecified |
K5289 | Other specified noninfective gastroenteritis and colitis |
K529 | Noninfective gastroenteritis and colitis, unspecified |
K580 | Irritable bowel syndrome with diarrhea |
K581 | Irritable bowel syndrome with constipation |
K582 | Mixed irritable bowel syndrome |
K588 | Other irritable bowel syndrome |
K589 | Irritable bowel syndrome without diarrhea |
K650 | Generalized (acute) peritonitis |
K652 | Spontaneous bacterial peritonitis |
K658 | Other peritonitis |
K6812 | Psoas muscle abscess |
K6819 | Other retroperitoneal abscess |
K682 | Retroperitoneal fibrosis |
K683 | Retroperitoneal hematoma |
K689 | Other disorders of retroperitoneum |
P768 | Other specified intestinal obstruction of newborn |
P769 | Intestinal obstruction of newborn, unspecified |
P771 | Stage 1 necrotizing enterocolitis in newborn |
P772 | Stage 2 necrotizing enterocolitis in newborn |
P773 | Stage 3 necrotizing enterocolitis in newborn |
P779 | Necrotizing enterocolitis in newborn, unspecified |
P781 | Other neonatal peritonitis |
P783 | Noninfective neonatal diarrhea |
P7881 | Congenital cirrhosis (of liver) |
P7882 | Peptic ulcer of newborn |
P7883 | Newborn esophageal reflux |
P7884 | Gestational alloimmune liver disease |
P7889 | Other specified perinatal digestive system disorders |
|
PDX Collection 6921 |
C965 | Multifocal and unisystemic Langerhans-cell histiocytosis |
C966 | Unifocal Langerhans-cell histiocytosis |
E71310 | Long chain/very long chain acyl CoA dehydrogenase deficiency |
E71311 | Medium chain acyl CoA dehydrogenase deficiency |
E71312 | Short chain acyl CoA dehydrogenase deficiency |
E71313 | Glutaric aciduria type II |
E71314 | Muscle carnitine palmitoyltransferase deficiency |
E71318 | Other disorders of fatty-acid oxidation |
E7132 | Disorders of ketone metabolism |
E7139 | Other disorders of fatty-acid metabolism |
E7140 | Disorder of carnitine metabolism, unspecified |
E7141 | Primary carnitine deficiency |
E7142 | Carnitine deficiency due to inborn errors of metabolism |
E7143 | Iatrogenic carnitine deficiency |
E71440 | Ruvalcaba-Myhre-Smith syndrome |
E71448 | Other secondary carnitine deficiency |
E7153 | Other group 2 peroxisomal disorders |
E803 | Defects of catalase and peroxidase |
E804 | Gilbert syndrome |
E805 | Crigler-Najjar syndrome |
E806 | Other disorders of bilirubin metabolism |
E807 | Disorder of bilirubin metabolism, unspecified |
E8840 | Mitochondrial metabolism disorder, unspecified |
E8841 | MELAS syndrome |
E8842 | MERRF syndrome |
E8843 | Disorders of mitochondrial tRNA synthetases |
E8849 | Other mitochondrial metabolism disorders |
E88811 | Insulin resistance syndrome, Type A |
E88818 | Other insulin resistance |
E88819 | Insulin resistance, unspecified |
E8889 | Other specified metabolic disorders |
H49811 | Kearns-Sayre syndrome, right eye |
H49812 | Kearns-Sayre syndrome, left eye |
H49813 | Kearns-Sayre syndrome, bilateral |
H49819 | Kearns-Sayre syndrome, unspecified eye |