PDX Collection 1040 (continued) |
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 |
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 |
P91821 | Neonatal cerebral infarction, right side of brain |
P91822 | Neonatal cerebral infarction, left side of brain |
P91823 | Neonatal cerebral infarction, bilateral |
P91829 | Neonatal cerebral infarction, unspecified side |
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 |
P91821 | Neonatal cerebral infarction, right side of brain |
P91822 | Neonatal cerebral infarction, left side of brain |
P91823 | Neonatal cerebral infarction, bilateral |
P91829 | Neonatal cerebral infarction, unspecified side |
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 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 |
Q200 | Common arterial trunk |
Q201 | Double outlet right ventricle |
Q202 | Double outlet left ventricle |
Q203 | Discordant ventriculoarterial connection |
Q204 | Double inlet ventricle |
Q205 | Discordant atrioventricular connection |
Q206 | Isomerism of atrial appendages |
Q208 | Other congenital malformations of cardiac chambers and connections |
Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
Q210 | Ventricular septal defect |
Q211 | Atrial septal defect |
Q212 | Atrioventricular septal defect |
Q213 | Tetralogy of Fallot |
Q214 | Aortopulmonary septal defect |
Q218 | Other congenital malformations of cardiac septa |
Q219 | Congenital malformation of cardiac septum, unspecified |
Q238 | Other congenital malformations of aortic and mitral valves |
Q239 | Congenital malformation of aortic and mitral valves, unspecified |
Q248 | Other specified congenital malformations of heart |
Q249 | Congenital malformation of heart, unspecified |
Q2730 | Arteriovenous malformation, site unspecified |
Q274 | Congenital phlebectasia |
Q280 | Arteriovenous malformation of precerebral vessels |
Q281 | Other malformations of precerebral vessels |
Q288 | Other specified congenital malformations of circulatory system |
Q289 | Congenital malformation of circulatory system, unspecified |
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 1058 |
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 |
Q200 | Common arterial trunk |
Q201 | Double outlet right ventricle |
Q202 | Double outlet left ventricle |
Q203 | Discordant ventriculoarterial connection |
Q204 | Double inlet ventricle |
Q205 | Discordant atrioventricular connection |
Q206 | Isomerism of atrial appendages |
Q208 | Other congenital malformations of cardiac chambers and connections |
Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
Q211 | Atrial septal defect |
Q212 | Atrioventricular septal defect |
Q213 | Tetralogy of Fallot |
Q214 | Aortopulmonary septal defect |
Q218 | Other congenital malformations of cardiac septa |
Q219 | Congenital malformation of cardiac septum, unspecified |
Q238 | Other congenital malformations of aortic and mitral valves |
Q239 | Congenital malformation of aortic and mitral valves, unspecified |
Q248 | Other specified congenital malformations of heart |
Q249 | Congenital malformation of heart, unspecified |
Q2730 | Arteriovenous malformation, site unspecified |
Q274 | Congenital phlebectasia |
Q280 | Arteriovenous malformation of precerebral vessels |
Q281 | Other malformations of precerebral vessels |
Q288 | Other specified congenital malformations of circulatory system |
Q289 | Congenital malformation of circulatory system, unspecified |
Q872 | Congenital malformation syndromes predominantly involving limbs |
Q873 | Congenital malformation syndromes involving early overgrowth |
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 |
|
PDX Collection 1060 |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
Q220 | Pulmonary valve atresia |
Q221 | Congenital pulmonary valve stenosis |
Q222 | Congenital pulmonary valve insufficiency |
Q223 | Other congenital malformations of pulmonary valve |
Q238 | Other congenital malformations of aortic and mitral valves |
Q239 | Congenital malformation of aortic and mitral valves, unspecified |
Q248 | Other specified congenital malformations of heart |
Q249 | Congenital malformation of heart, unspecified |
Q2730 | Arteriovenous malformation, site unspecified |
Q274 | Congenital phlebectasia |
Q280 | Arteriovenous malformation of precerebral vessels |
Q281 | Other malformations of precerebral vessels |
Q288 | Other specified congenital malformations of circulatory system |
Q289 | Congenital malformation of circulatory system, unspecified |
Q872 | Congenital malformation syndromes predominantly involving limbs |
Q873 | Congenital malformation syndromes involving early overgrowth |