PDX Collection 6835 (continued) |
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 |
D564 | Hereditary persistence of fetal hemoglobin [HPFH] |
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 |
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 |
D759 | Disease of blood and blood-forming organs, unspecified |
P612 | Anemia of prematurity |
P613 | Congenital anemia from fetal blood loss |
P614 | Other congenital anemias, not elsewhere classified |
|
PDX Collection 6836 |
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 |
D553 | Anemia due to disorders of nucleotide metabolism |
D558 | Other anemias due to enzyme disorders |
D559 | Anemia due to enzyme disorder, unspecified |
D564 | Hereditary persistence of fetal hemoglobin [HPFH] |
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 |
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 |
D759 | Disease of blood and blood-forming organs, unspecified |
P612 | Anemia of prematurity |
P613 | Congenital anemia from fetal blood loss |
P614 | Other congenital anemias, not elsewhere classified |
|
PDX Collection 6837 |
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 |
D564 | Hereditary persistence of fetal hemoglobin [HPFH] |
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 |
D573 | Sickle-cell trait |
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 |
D582 | Other hemoglobinopathies |
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 |
D5930 | Hemolytic-uremic syndrome, unspecified |
D5931 | Infection-associated hemolytic-uremic syndrome |
D5932 | Hereditary hemolytic-uremic syndrome |
D5939 | Other hemolytic-uremic syndrome |
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 |
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 |
D759 | Disease of blood and blood-forming organs, unspecified |
P615 | Transient neonatal neutropenia |
P618 | Other specified perinatal hematological disorders |
P619 | Perinatal hematological disorder, unspecified |
|
PDX Collection 6838 |
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 |
I2481 | Acute coronary microvascular dysfunction |
I2489 | Other forms of acute ischemic heart disease |
I249 | Acute ischemic heart disease, unspecified |
I2510 | Atherosclerotic heart disease of native coronary artery without angina pectoris |
I25110 | Atherosclerotic heart disease of native coronary artery with unstable angina pectoris |
I25111 | Atherosclerotic heart disease of native coronary artery with angina pectoris with documented spasm |
I25112 | Atherosclerotic heart disease of native coronary artery with refractory angina pectoris |
I25118 | Atherosclerotic heart disease of native coronary artery with other forms of angina pectoris |
I25119 | Atherosclerotic heart disease of native coronary artery with unspecified angina pectoris |
I255 | Ischemic cardiomyopathy |
I256 | Silent myocardial ischemia |
I25700 | Atherosclerosis of coronary artery bypass graft(s), unspecified, with unstable angina pectoris |
I25701 | Atherosclerosis of coronary artery bypass graft(s), unspecified, with angina pectoris with documented spasm |
I25702 | Atherosclerosis of coronary artery bypass graft(s), unspecified, with refractory angina pectoris |
I25708 | Atherosclerosis of coronary artery bypass graft(s), unspecified, with other forms of angina pectoris |
I25709 | Atherosclerosis of coronary artery bypass graft(s), unspecified, with unspecified angina pectoris |
I25710 | Atherosclerosis of autologous vein coronary artery bypass graft(s) with unstable angina pectoris |
I25711 | Atherosclerosis of autologous vein coronary artery bypass graft(s) with angina pectoris with documented spasm |
I25712 | Atherosclerosis of autologous vein coronary artery bypass graft(s) with refractory angina pectoris |
I25718 | Atherosclerosis of autologous vein coronary artery bypass graft(s) with other forms of angina pectoris |
I25719 | Atherosclerosis of autologous vein coronary artery bypass graft(s) with unspecified angina pectoris |
I25720 | Atherosclerosis of autologous artery coronary artery bypass graft(s) with unstable angina pectoris |
I25721 | Atherosclerosis of autologous artery coronary artery bypass graft(s) with angina pectoris with documented spasm |
I25722 | Atherosclerosis of autologous artery coronary artery bypass graft(s) with refractory angina pectoris |
I25728 | Atherosclerosis of autologous artery coronary artery bypass graft(s) with other forms of angina pectoris |
I25729 | Atherosclerosis of autologous artery coronary artery bypass graft(s) with unspecified angina pectoris |
I25730 | Atherosclerosis of nonautologous biological coronary artery bypass graft(s) with unstable angina pectoris |
I25731 | Atherosclerosis of nonautologous biological coronary artery bypass graft(s) with angina pectoris with documented spasm |
I25732 | Atherosclerosis of nonautologous biological coronary artery bypass graft(s) with refractory angina pectoris |
I25738 | Atherosclerosis of nonautologous biological coronary artery bypass graft(s) with other forms of angina pectoris |
I25739 | Atherosclerosis of nonautologous biological coronary artery bypass graft(s) with unspecified angina pectoris |
I25750 | Atherosclerosis of native coronary artery of transplanted heart with unstable angina |
I25751 | Atherosclerosis of native coronary artery of transplanted heart with angina pectoris with documented spasm |
I25752 | Atherosclerosis of native coronary artery of transplanted heart with refractory angina pectoris |
I25759 | Atherosclerosis of native coronary artery of transplanted heart with unspecified angina pectoris |
I25760 | Atherosclerosis of bypass graft of coronary artery of transplanted heart with unstable angina |
I25761 | Atherosclerosis of bypass graft of coronary artery of transplanted heart with angina pectoris with documented spasm |
I25762 | Atherosclerosis of bypass graft of coronary artery of transplanted heart with refractory angina pectoris |
I25768 | Atherosclerosis of bypass graft of coronary artery of transplanted heart with other forms of angina pectoris |
I25769 | Atherosclerosis of bypass graft of coronary artery of transplanted heart with unspecified angina pectoris |
I25790 | Atherosclerosis of other coronary artery bypass graft(s) with unstable angina pectoris |
I25791 | Atherosclerosis of other coronary artery bypass graft(s) with angina pectoris with documented spasm |
I25792 | Atherosclerosis of other coronary artery bypass graft(s) with refractory angina pectoris |
I25798 | Atherosclerosis of other coronary artery bypass graft(s) with other forms of angina pectoris |
I25799 | Atherosclerosis of other coronary artery bypass graft(s) with unspecified angina pectoris |
I25812 | Atherosclerosis of bypass graft of coronary artery of transplanted heart without 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 |
R570 | Cardiogenic shock |
R579 | Shock, unspecified |
|
PDX Collection 6839 |
G802 | Spastic hemiplegic cerebral palsy |
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 |
I6783 | Posterior reversible encephalopathy syndrome |
|
PDX Collection 6840 |
G801 | Spastic diplegic cerebral palsy |
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 |
I6783 | Posterior reversible encephalopathy syndrome |
|
PDX Collection 6841 |
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 |
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 |
G2570 | Drug induced movement disorder, unspecified |
G2571 | Drug induced akathisia |
G2579 | Other drug induced movement disorders |
G2589 | Other specified extrapyramidal and movement disorders |
G259 | Extrapyramidal and movement disorder, 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 |
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 |
I6783 | Posterior reversible encephalopathy syndrome |
|
PDX Collection 6842 |
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 |
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 |