PDX Collection 1040 (continued) |
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 |
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 |
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 |
P918 | 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 |
P918 | 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 |
P293 | 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 |
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 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 1059 |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
P293 | Persistent fetal circulation |
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 |
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 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 |
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 |