|
PDX Collection 1487 |
P390 | Neonatal infective mastitis |
P392 | Intra-amniotic infection affecting newborn, not elsewhere classified |
P394 | Neonatal skin infection |
P398 | Other specified infections specific to the perinatal period |
P399 | Infection specific to the perinatal period, unspecified |
|
PDX Collection 1488 |
A021 | Salmonella sepsis |
A207 | Septicemic plague |
A227 | Anthrax sepsis |
A392 | Acute meningococcemia |
A393 | Chronic meningococcemia |
A394 | Meningococcemia, unspecified |
A409 | Streptococcal sepsis, unspecified |
A4101 | Sepsis due to Methicillin susceptible Staphylococcus aureus |
A4102 | Sepsis due to Methicillin resistant Staphylococcus aureus |
A411 | Sepsis due to other specified staphylococcus |
A412 | Sepsis due to unspecified staphylococcus |
A413 | Sepsis due to Hemophilus influenzae |
A414 | Sepsis due to anaerobes |
A4150 | Gram-negative sepsis, unspecified |
A4151 | Sepsis due to Escherichia coli [E. coli] |
A4152 | Sepsis due to Pseudomonas |
A4153 | Sepsis due to Serratia |
A4154 | Sepsis due to Acinetobacter baumannii |
A4159 | Other Gram-negative sepsis |
A4181 | Sepsis due to Enterococcus |
A4189 | Other specified sepsis |
A419 | Sepsis, unspecified organism |
A427 | Actinomycotic sepsis |
A482 | Nonpneumonic Legionnaires' disease [Pontiac fever] |
A484 | Brazilian purpuric fever |
A488 | Other specified bacterial diseases |
A4901 | Methicillin susceptible Staphylococcus aureus infection, unspecified site |
A4902 | Methicillin resistant Staphylococcus aureus infection, unspecified site |
A491 | Streptococcal infection, unspecified site |
A492 | Hemophilus influenzae infection, unspecified site |
A493 | Mycoplasma infection, unspecified site |
A498 | Other bacterial infections of unspecified site |
A499 | Bacterial infection, unspecified |
B007 | Disseminated herpesviral disease |
B92 | Sequelae of leprosy |
B942 | Sequelae of viral hepatitis |
B948 | Sequelae of other specified infectious and parasitic diseases |
B949 | Sequelae of unspecified infectious and parasitic disease |
P392 | Intra-amniotic infection affecting newborn, not elsewhere classified |
P393 | Neonatal urinary tract infection |
P394 | Neonatal skin infection |
P398 | Other specified infections specific to the perinatal period |
P399 | Infection specific to the perinatal period, unspecified |
P95 | Stillbirth |
P969 | Condition originating in the perinatal period, unspecified |
R7881 | Bacteremia |
|
PDX Collection 1489 |
A499 | Bacterial infection, unspecified |
N10 | Acute pyelonephritis |
N110 | Nonobstructive reflux-associated chronic pyelonephritis |
N118 | Other chronic tubulo-interstitial nephritis |
N119 | Chronic tubulo-interstitial nephritis, unspecified |
N12 | Tubulo-interstitial nephritis, not specified as acute or chronic |
N136 | Pyonephrosis |
N151 | Renal and perinephric abscess |
N2882 | Megaloureter |
N2884 | Pyelitis cystica |
N2885 | Pyeloureteritis cystica |
N2886 | Ureteritis cystica |
N2889 | Other specified disorders of kidney and ureter |
N289 | Disorder of kidney and ureter, unspecified |
N3000 | Acute cystitis without hematuria |
N3001 | Acute cystitis with hematuria |
N3010 | Interstitial cystitis (chronic) without hematuria |
N3011 | Interstitial cystitis (chronic) with hematuria |
N3020 | Other chronic cystitis without hematuria |
N3021 | Other chronic cystitis with hematuria |
N3030 | Trigonitis without hematuria |
N3031 | Trigonitis with hematuria |
N3080 | Other cystitis without hematuria |
N3081 | Other cystitis with hematuria |
N3090 | Cystitis, unspecified without hematuria |
N3091 | Cystitis, unspecified with hematuria |
N369 | Urethral disorder, unspecified |
N390 | Urinary tract infection, site not specified |
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 |
N99511 | Cystostomy infection |
P392 | Intra-amniotic infection affecting newborn, not elsewhere classified |
P393 | Neonatal urinary tract infection |
P394 | Neonatal skin infection |
P398 | Other specified infections specific to the perinatal period |
P399 | Infection specific to the perinatal period, unspecified |
R300 | Dysuria |
R309 | Painful micturition, unspecified |
R8271 | Bacteriuria |
T83511A | Infection and inflammatory reaction due to indwelling urethral catheter, initial encounter |
|
PDX Collection 1490 |
P290 | Neonatal cardiac failure |
P2911 | Neonatal tachycardia |
P2912 | Neonatal bradycardia |
P292 | Neonatal hypertension |
P294 | Transient myocardial ischemia in newborn |
P2989 | Other cardiovascular disorders originating in the perinatal period |
P299 | Cardiovascular disorder originating in the perinatal period, unspecified |
P53 | Hemorrhagic disease of newborn |
P60 | Disseminated intravascular coagulation of newborn |
P610 | Transient neonatal thrombocytopenia |
P611 | Polycythemia neonatorum |
P612 | Anemia of prematurity |
P613 | Congenital anemia from fetal blood loss |
P614 | Other congenital anemias, not elsewhere classified |
P615 | Transient neonatal neutropenia |
P616 | Other transient neonatal disorders of coagulation |
P618 | Other specified perinatal hematological disorders |
P619 | Perinatal hematological disorder, unspecified |
P941 | Congenital hypertonia |
P942 | Congenital hypotonia |
P948 | Other disorders of muscle tone of newborn |
P949 | Disorder of muscle tone of newborn, unspecified |
P960 | Congenital renal failure |
P963 | Wide cranial sutures of newborn |
P965 | Complication to newborn due to (fetal) intrauterine procedure |
P9682 | Delayed separation of umbilical cord |
P9683 | Meconium staining |
P9689 | Other specified conditions originating in the perinatal period |
|
PDX Collection 1491 |
P290 | Neonatal cardiac failure |
P2911 | Neonatal tachycardia |
P2912 | Neonatal bradycardia |
P292 | Neonatal hypertension |
P294 | Transient myocardial ischemia in newborn |
P2989 | Other cardiovascular disorders originating in the perinatal period |
P299 | Cardiovascular disorder originating in the perinatal period, unspecified |
P500 | Newborn affected by intrauterine (fetal) blood loss from vasa previa |
P501 | Newborn affected by intrauterine (fetal) blood loss from ruptured cord |
P502 | Newborn affected by intrauterine (fetal) blood loss from placenta |
P503 | Newborn affected by hemorrhage into co-twin |
P504 | Newborn affected by hemorrhage into maternal circulation |
P505 | Newborn affected by intrauterine (fetal) blood loss from cut end of co-twin's cord |
P508 | Newborn affected by other intrauterine (fetal) blood loss |
P509 | Newborn affected by intrauterine (fetal) blood loss, unspecified |
P53 | Hemorrhagic disease of newborn |
P540 | Neonatal hematemesis |
P541 | Neonatal melena |
P542 | Neonatal rectal hemorrhage |
P543 | Other neonatal gastrointestinal hemorrhage |
P544 | Neonatal adrenal hemorrhage |
P546 | Neonatal vaginal hemorrhage |
P548 | Other specified neonatal hemorrhages |
P549 | Neonatal hemorrhage, unspecified |
P60 | Disseminated intravascular coagulation of newborn |
P610 | Transient neonatal thrombocytopenia |
P611 | Polycythemia neonatorum |
P612 | Anemia of prematurity |
P613 | Congenital anemia from fetal blood loss |
P614 | Other congenital anemias, not elsewhere classified |
P615 | Transient neonatal neutropenia |
P616 | Other transient neonatal disorders of coagulation |
P618 | Other specified perinatal hematological disorders |
P619 | Perinatal hematological disorder, unspecified |
P941 | Congenital hypertonia |
P942 | Congenital hypotonia |
P948 | Other disorders of muscle tone of newborn |
P949 | Disorder of muscle tone of newborn, unspecified |
P960 | Congenital renal failure |
P963 | Wide cranial sutures of newborn |
P965 | Complication to newborn due to (fetal) intrauterine procedure |
P9682 | Delayed separation of umbilical cord |
P9683 | Meconium staining |
P9689 | Other specified conditions originating in the perinatal period |
|
PDX Collection 1492 |
P290 | Neonatal cardiac failure |
P2911 | Neonatal tachycardia |
P2912 | Neonatal bradycardia |
P292 | Neonatal hypertension |
P294 | Transient myocardial ischemia in newborn |
P2989 | Other cardiovascular disorders originating in the perinatal period |
P299 | Cardiovascular disorder originating in the perinatal period, unspecified |
P550 | Rh isoimmunization of newborn |
P551 | ABO isoimmunization of newborn |
P558 | Other hemolytic diseases of newborn |
P559 | Hemolytic disease of newborn, unspecified |
P560 | Hydrops fetalis due to isoimmunization |
P5690 | Hydrops fetalis due to unspecified hemolytic disease |
P5699 | Hydrops fetalis due to other hemolytic disease |
P570 | Kernicterus due to isoimmunization |
P941 | Congenital hypertonia |
P942 | Congenital hypotonia |
P948 | Other disorders of muscle tone of newborn |
P949 | Disorder of muscle tone of newborn, unspecified |
P960 | Congenital renal failure |
P963 | Wide cranial sutures of newborn |
P965 | Complication to newborn due to (fetal) intrauterine procedure |
P9682 | Delayed separation of umbilical cord |
P9683 | Meconium staining |
P9689 | Other specified conditions originating in the perinatal period |
|
PDX Collection 1493 |
P290 | Neonatal cardiac failure |
P2911 | Neonatal tachycardia |
P2912 | Neonatal bradycardia |
P292 | Neonatal hypertension |
P294 | Transient myocardial ischemia in newborn |
P2989 | Other cardiovascular disorders originating in the perinatal period |
P299 | Cardiovascular disorder originating in the perinatal period, unspecified |
P578 | Other specified kernicterus |
P579 | Kernicterus, unspecified |
P580 | Neonatal jaundice due to bruising |
P581 | Neonatal jaundice due to bleeding |
P582 | Neonatal jaundice due to infection |
P583 | Neonatal jaundice due to polycythemia |
P5841 | Neonatal jaundice due to drugs or toxins transmitted from mother |
P5842 | Neonatal jaundice due to drugs or toxins given to newborn |
P585 | Neonatal jaundice due to swallowed maternal blood |
P588 | Neonatal jaundice due to other specified excessive hemolysis |
P589 | Neonatal jaundice due to excessive hemolysis, unspecified |
P590 | Neonatal jaundice associated with preterm delivery |
P591 | Inspissated bile syndrome |
P5920 | Neonatal jaundice from unspecified hepatocellular damage |
P5929 | Neonatal jaundice from other hepatocellular damage |
P593 | Neonatal jaundice from breast milk inhibitor |
P598 | Neonatal jaundice from other specified causes |
P599 | Neonatal jaundice, unspecified |
P941 | Congenital hypertonia |
P942 | Congenital hypotonia |
P948 | Other disorders of muscle tone of newborn |
P949 | Disorder of muscle tone of newborn, unspecified |
P960 | Congenital renal failure |
P963 | Wide cranial sutures of newborn |
P965 | Complication to newborn due to (fetal) intrauterine procedure |
P9682 | Delayed separation of umbilical cord |
P9683 | Meconium staining |
P9689 | Other specified conditions originating in the perinatal period |
|
PDX Collection 1494 |
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 |
D6103 | Fanconi anemia |
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 1495 |
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 |
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 |
D6103 | Fanconi anemia |
D6109 | Other constitutional aplastic anemia |