|
PDX Collection 1508 |
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 1509 |
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 1510 |
P830 | Sclerema neonatorum |
P8330 | Unspecified edema specific to newborn |
P8339 | Other edema specific to newborn |
|
PDX Collection 1511 |
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 1512 |
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 1513 |
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 |
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 1514 |
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 |
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 1515 |
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 1516 |
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 |
|
PDX Collection 1517 |
P9201 | Bilious vomiting of newborn |
P9209 | Other vomiting of newborn |
|
PDX Collection 1518 |
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 1519 |
Q000 | Anencephaly |
Q001 | Craniorachischisis |
Q002 | Iniencephaly |
|
PDX Collection 1520 |
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 1521 |
Q044 | Septo-optic dysplasia of brain |
Q045 | Megalencephaly |
Q046 | Congenital cerebral cysts |
Q048 | Other specified congenital malformations of brain |
|
PDX Collection 1522 |
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 |
Q8711 | Prader-Willi syndrome |
Q8719 | Other congenital malformation syndromes predominantly associated with short stature |
Q872 | Congenital malformation syndromes predominantly involving limbs |
Q873 | Congenital malformation syndromes involving early overgrowth |
Q8740 | Marfan syndrome, unspecified |
Q87410 | Marfan syndrome with aortic dilation |
Q87418 | Marfan syndrome with other cardiovascular manifestations |
Q8742 | Marfan syndrome with ocular manifestations |
Q8743 | Marfan syndrome with skeletal manifestation |
Q875 | Other congenital malformation syndromes with other skeletal changes |
Q8781 | Alport syndrome |
Q8782 | Arterial tortuosity syndrome |
Q8783 | Bardet-Biedl syndrome |
Q8784 | Laurence-Moon syndrome |
Q8785 | MED13L 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 1523 |
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 |
Q2110 | Atrial septal defect, unspecified |
Q2111 | Secundum atrial septal defect |
Q2112 | Patent foramen ovale |
Q2113 | Coronary sinus atrial septal defect |
Q2114 | Superior sinus venosus atrial septal defect |
Q2115 | Inferior sinus venosus atrial septal defect |
Q2116 | Sinus venosus atrial septal defect, unspecified |
Q2119 | Other specified atrial septal defect |
Q2120 | Atrioventricular septal defect, unspecified as to partial or complete |
Q2121 | Partial atrioventricular septal defect |
Q2122 | Transitional atrioventricular septal defect |
Q2123 | Complete 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 |
Q8711 | Prader-Willi syndrome |
Q8719 | Other congenital malformation syndromes predominantly associated with short stature |
Q872 | Congenital malformation syndromes predominantly involving limbs |
Q873 | Congenital malformation syndromes involving early overgrowth |
Q8740 | Marfan syndrome, unspecified |
Q87410 | Marfan syndrome with aortic dilation |
Q87418 | Marfan syndrome with other cardiovascular manifestations |
Q8742 | Marfan syndrome with ocular manifestations |
Q8743 | Marfan syndrome with skeletal manifestation |
Q875 | Other congenital malformation syndromes with other skeletal changes |
Q8781 | Alport syndrome |
Q8782 | Arterial tortuosity syndrome |
Q8783 | Bardet-Biedl syndrome |
Q8784 | Laurence-Moon syndrome |
Q8785 | MED13L 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 1524 |
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 |
Q2110 | Atrial septal defect, unspecified |
Q2111 | Secundum atrial septal defect |
Q2112 | Patent foramen ovale |
Q2113 | Coronary sinus atrial septal defect |
Q2114 | Superior sinus venosus atrial septal defect |
Q2115 | Inferior sinus venosus atrial septal defect |
Q2116 | Sinus venosus atrial septal defect, unspecified |
Q2119 | Other specified atrial septal defect |
Q2120 | Atrioventricular septal defect, unspecified as to partial or complete |
Q2121 | Partial atrioventricular septal defect |
Q2122 | Transitional atrioventricular septal defect |
Q2123 | Complete 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 syndrome, unspecified |
Q87410 | Marfan syndrome with aortic dilation |
Q87418 | Marfan syndrome with other cardiovascular manifestations |
Q8742 | Marfan syndrome with ocular manifestations |
Q8743 | Marfan syndrome with skeletal manifestation |
Q875 | Other congenital malformation syndromes with other skeletal changes |
Q8781 | Alport syndrome |
Q8782 | Arterial tortuosity syndrome |
Q8783 | Bardet-Biedl syndrome |
Q8784 | Laurence-Moon syndrome |
Q8785 | MED13L 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 1525 |
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 |
Q2110 | Atrial septal defect, unspecified |
Q2111 | Secundum atrial septal defect |
Q2112 | Patent foramen ovale |
Q2113 | Coronary sinus atrial septal defect |
Q2114 | Superior sinus venosus atrial septal defect |
Q2115 | Inferior sinus venosus atrial septal defect |
Q2116 | Sinus venosus atrial septal defect, unspecified |
Q2119 | Other specified atrial septal defect |
Q2120 | Atrioventricular septal defect, unspecified as to partial or complete |
Q2121 | Partial atrioventricular septal defect |
Q2122 | Transitional atrioventricular septal defect |
Q2123 | Complete 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 |
Q8781 | Alport syndrome |
Q8782 | Arterial tortuosity syndrome |
|
PDX Collection 1526 |
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 |