| PDX Collection 1036 (continued) |
| 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 1037 |
| 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 1038 |
| 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 1039 |
| 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 |
| D552 | Anemia due to 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 |
| 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 |
| D591 | Other autoimmune hemolytic anemias |
| D592 | Drug-induced nonautoimmune hemolytic anemia |
| D593 | 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 |
| 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 |
| D630 | Anemia in neoplastic disease |
| D631 | Anemia in chronic kidney disease |
| D638 | Anemia in other chronic diseases classified elsewhere |
| D640 | Hereditary sideroblastic anemia |
| D641 | Secondary sideroblastic anemia due to disease |
| 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 1040 |
| 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 |
| D591 | Other autoimmune hemolytic anemias |
| D593 | 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 |
| 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 |
| D630 | Anemia in neoplastic disease |
| D631 | Anemia in chronic kidney disease |
| D638 | Anemia in other chronic diseases classified elsewhere |
| D640 | Hereditary sideroblastic anemia |
| D641 | Secondary sideroblastic anemia due to disease |
| 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 1041 |
| 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 |
| P700 | Syndrome of infant of mother with gestational diabetes |
| P701 | Syndrome of infant of a diabetic mother |
| P702 | Neonatal diabetes mellitus |
| P703 | Iatrogenic neonatal hypoglycemia |
| P704 | Other neonatal hypoglycemia |
| P709 | Transitory disorder of carbohydrate metabolism of newborn, unspecified |
| P710 | Cow's milk hypocalcemia in newborn |
| P711 | Other neonatal hypocalcemia |
| P712 | Neonatal hypomagnesemia |
| P713 | Neonatal tetany without calcium or magnesium deficiency |
| P714 | Transitory neonatal hypoparathyroidism |
| P718 | Other transitory neonatal disorders of calcium and magnesium metabolism |
| P719 | Transitory neonatal disorder of calcium and magnesium metabolism, unspecified |
| P721 | Transitory neonatal hyperthyroidism |
| P729 | Transitory neonatal endocrine disorder, unspecified |
| P740 | Late metabolic acidosis of newborn |
| P741 | Dehydration of newborn |
| P742 | Disturbances of sodium balance of newborn |
| P743 | Disturbances of potassium balance of newborn |
| P744 | Other transitory electrolyte disturbances of newborn |
| P749 | Transitory metabolic disturbance of newborn, unspecified |
| P940 | Transient neonatal myasthenia gravis |
| 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 1042 |
| P700 | Syndrome of infant of mother with gestational diabetes |
| P701 | Syndrome of infant of a diabetic mother |
| P702 | Neonatal diabetes mellitus |
| P703 | Iatrogenic neonatal hypoglycemia |
| P704 | Other neonatal hypoglycemia |
| P709 | Transitory disorder of carbohydrate metabolism of newborn, unspecified |
| P710 | Cow's milk hypocalcemia in newborn |
| P711 | Other neonatal hypocalcemia |
| P712 | Neonatal hypomagnesemia |
| P713 | Neonatal tetany without calcium or magnesium deficiency |
| P714 | Transitory neonatal hypoparathyroidism |
| P718 | Other transitory neonatal disorders of calcium and magnesium metabolism |
| P719 | Transitory neonatal disorder of calcium and magnesium metabolism, unspecified |
| P721 | Transitory neonatal hyperthyroidism |
| P729 | Transitory neonatal endocrine disorder, unspecified |
| P740 | Late metabolic acidosis of newborn |
| P741 | Dehydration of newborn |
| P742 | Disturbances of sodium balance of newborn |
| P743 | Disturbances of potassium balance of newborn |
| P744 | Other transitory electrolyte disturbances of newborn |
| P749 | Transitory metabolic disturbance of newborn, unspecified |
| P940 | Transient neonatal myasthenia gravis |
| |
| PDX Collection 1043 |
| P760 | Meconium plug syndrome |
| P761 | Transitory ileus of newborn |
| P762 | Intestinal obstruction due to inspissated milk |
| 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 |
| P780 | Perinatal intestinal perforation |
| P781 | Other neonatal peritonitis |
| P782 | Neonatal hematemesis and melena due to swallowed maternal blood |
| 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 |
| P789 | Perinatal digestive system disorder, unspecified |
| |
| PDX Collection 1044 |
| 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 |
| P760 | Meconium plug syndrome |
| P761 | Transitory ileus of newborn |
| P762 | Intestinal obstruction due to inspissated milk |
| 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 |
| P780 | Perinatal intestinal perforation |
| P781 | Other neonatal peritonitis |
| P782 | Neonatal hematemesis and melena due to swallowed maternal blood |
| 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 |
| P789 | Perinatal digestive system 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 1045 |
| P830 | Sclerema neonatorum |
| P8330 | Unspecified edema specific to newborn |
| P8339 | Other edema specific to newborn |
| |
| PDX Collection 1046 |
| 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 |
| P832 | Hydrops fetalis not due to hemolytic disease |
| 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 1047 |
| P800 | Cold injury syndrome |
| P808 | Other hypothermia of newborn |
| P809 | Hypothermia of newborn, unspecified |
| P810 | Environmental hyperthermia of newborn |
| P818 | Other specified disturbances of temperature regulation of newborn |
| P819 | Disturbance of temperature regulation of newborn, unspecified |
| P830 | Sclerema neonatorum |
| P8330 | Unspecified edema specific to newborn |
| P8339 | Other edema specific to newborn |
| |
| PDX Collection 1048 |
| 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 |
| P90 | Convulsions of newborn |
| P91811 | Neonatal encephalopathy in diseases classified elsewhere |
| P91819 | Neonatal encephalopathy, unspecified |
| P9188 | Other specified disturbances of cerebral status of newborn |
| P919 | Disturbance of cerebral status of newborn, 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 1049 |
| P90 | Convulsions of newborn |
| P910 | Neonatal cerebral ischemia |
| P911 | Acquired periventricular cysts of newborn |
| P913 | Neonatal cerebral irritability |
| P914 | Neonatal cerebral depression |
| P915 | Neonatal coma |
| P91811 | Neonatal encephalopathy in diseases classified elsewhere |
| P91819 | Neonatal encephalopathy, unspecified |
| P9188 | Other specified disturbances of cerebral status of newborn |
| P919 | Disturbance of cerebral status of newborn, unspecified |
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