| PDX Collection 1039 (continued) |
| 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 |
| P7421 | Hypernatremia of newborn |
| P7422 | Hyponatremia of newborn |
| P7431 | Hyperkalemia of newborn |
| P7432 | Hypokalemia of newborn |
| P7441 | Alkalosis of newborn |
| P74421 | Hyperchloremia of newborn |
| P74422 | Hypochloremia of newborn |
| P7449 | Other transitory electrolyte disturbance 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 |
| P7421 | Hypernatremia of newborn |
| P7422 | Hyponatremia of newborn |
| P7431 | Hyperkalemia of newborn |
| P7432 | Hypokalemia of newborn |
| P7441 | Alkalosis of newborn |
| P74421 | Hyperchloremia of newborn |
| P74422 | Hypochloremia of newborn |
| P7449 | Other transitory electrolyte disturbance 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 |
| |
| PDX Collection 1050 |
| P84 | Other problems with newborn |
| P9160 | Hypoxic ischemic encephalopathy [HIE], unspecified |
| P9161 | Mild hypoxic ischemic encephalopathy [HIE] |
| P9162 | Moderate hypoxic ischemic encephalopathy [HIE] |
| P9163 | Severe hypoxic ischemic encephalopathy [HIE] |
| |
| PDX Collection 1051 |
| P9201 | Bilious vomiting of newborn |
| P9209 | Other vomiting of newborn |
| |
| PDX Collection 1052 |
| P930 | Grey baby syndrome |
| P938 | Other reactions and intoxications due to drugs administered to newborn |
| P961 | Neonatal withdrawal symptoms from maternal use of drugs of addiction |
| P962 | Withdrawal symptoms from therapeutic use of drugs in newborn |
| |
| PDX Collection 1053 |
| Q000 | Anencephaly |
| Q001 | Craniorachischisis |
| Q002 | Iniencephaly |
| |
| PDX Collection 1054 |
| Q010 | Frontal encephalocele |
| Q011 | Nasofrontal encephalocele |
| Q012 | Occipital encephalocele |
| Q018 | Encephalocele of other sites |
| Q019 | Encephalocele, unspecified |
| Q02 | Microcephaly |
| Q040 | Congenital malformations of corpus callosum |
| Q041 | Arhinencephaly |
| Q042 | Holoprosencephaly |
| Q043 | Other reduction deformities of brain |
| Q044 | Septo-optic dysplasia of brain |
| Q045 | Megalencephaly |
| Q046 | Congenital cerebral cysts |
| Q048 | Other specified congenital malformations of brain |
| |
| PDX Collection 1055 |
| Q044 | Septo-optic dysplasia of brain |
| Q045 | Megalencephaly |
| Q046 | Congenital cerebral cysts |
| Q048 | Other specified congenital malformations of brain |
| |
| PDX Collection 1056 |
| E7871 | Barth syndrome |
| E7872 | Smith-Lemli-Opitz syndrome |
| G901 | Familial dysautonomia [Riley-Day] |
| Q050 | Cervical spina bifida with hydrocephalus |
| Q051 | Thoracic spina bifida with hydrocephalus |
| Q052 | Lumbar spina bifida with hydrocephalus |
| Q053 | Sacral spina bifida with hydrocephalus |
| Q054 | Unspecified spina bifida with hydrocephalus |
| Q055 | Cervical spina bifida without hydrocephalus |
| Q056 | Thoracic spina bifida without hydrocephalus |
| Q057 | Lumbar spina bifida without hydrocephalus |
| Q058 | Sacral spina bifida without hydrocephalus |
| Q059 | Spina bifida, unspecified |
| Q060 | Amyelia |
| Q061 | Hypoplasia and dysplasia of spinal cord |
| Q063 | Other congenital cauda equina malformations |
| Q068 | Other specified congenital malformations of spinal cord |
| Q069 | Congenital malformation of spinal cord, unspecified |
| Q0700 | Arnold-Chiari syndrome without spina bifida or hydrocephalus |
| Q0701 | Arnold-Chiari syndrome with spina bifida |
| Q0702 | Arnold-Chiari syndrome with hydrocephalus |
| Q0703 | Arnold-Chiari syndrome with spina bifida and hydrocephalus |
| Q078 | Other specified congenital malformations of nervous system |
| Q079 | Congenital malformation of nervous system, unspecified |
| Q871 | Congenital malformation syndromes predominantly associated with short stature |
| Q872 | Congenital malformation syndromes predominantly involving limbs |
| Q873 | Congenital malformation syndromes involving early overgrowth |
| Q8740 | Marfan's syndrome, unspecified |
| Q87410 | Marfan's syndrome with aortic dilation |
| Q87418 | Marfan's syndrome with other cardiovascular manifestations |
| Q8742 | Marfan's syndrome with ocular manifestations |
| Q8743 | Marfan's syndrome with skeletal manifestation |
| Q875 | Other congenital malformation syndromes with other skeletal changes |
| Q8781 | Alport syndrome |
| Q8782 | Arterial tortuosity syndrome |
| Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
| Q897 | Multiple congenital malformations, not elsewhere classified |
| Q898 | Other specified congenital malformations |
| Q992 | Fragile X chromosome |
| |
| PDX Collection 1057 |
| E7871 | Barth syndrome |
| E7872 | Smith-Lemli-Opitz syndrome |
| I230 | Hemopericardium as current complication following acute myocardial infarction |
| I231 | Atrial septal defect as current complication following acute myocardial infarction |
| I232 | Ventricular septal defect as current complication following acute myocardial infarction |
| I233 | Rupture of cardiac wall without hemopericardium as current complication following acute myocardial infarction |
| I236 | Thrombosis of atrium, auricular appendage, and ventricle as current complications following acute myocardial infarction |
| I237 | Postinfarction angina |
| I238 | Other current complications following acute myocardial infarction |
| I510 | Cardiac septal defect, acquired |
| P2930 | Pulmonary hypertension of newborn |
| P2938 | Other persistent fetal circulation |
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