PDX Collection 1056:38 codes |
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 |
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 1057:51 codes |
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 |
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 1058:42 codes |
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 |
Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
Q897 | Multiple congenital malformations, not elsewhere classified |
Q898 | Other specified congenital malformations |
|
PDX Collection 1059:32 codes |
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 |
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 1060:24 codes |
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 |
Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
Q897 | Multiple congenital malformations, not elsewhere classified |
Q898 | Other specified congenital malformations |
|
PDX Collection 1061:38 codes |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
P293 | Persistent fetal circulation |
Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
Q224 | Congenital tricuspid stenosis |
Q225 | Ebstein's anomaly |
Q226 | Hypoplastic right heart syndrome |
Q228 | Other congenital malformations of tricuspid valve |
Q229 | Congenital malformation of tricuspid valve, unspecified |
Q230 | Congenital stenosis of aortic valve |
Q231 | Congenital insufficiency of aortic valve |
Q232 | Congenital mitral stenosis |
Q233 | Congenital mitral insufficiency |
Q234 | Hypoplastic left heart syndrome |
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 |
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 1062:25 codes |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
Q238 | Other congenital malformations of aortic and mitral valves |
Q239 | Congenital malformation of aortic and mitral valves, unspecified |
Q240 | Dextrocardia |
Q241 | Levocardia |
Q242 | Cor triatriatum |
Q243 | Pulmonary infundibular stenosis |
Q244 | Congenital subaortic stenosis |
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 |
Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
Q897 | Multiple congenital malformations, not elsewhere classified |
Q898 | Other specified congenital malformations |
|
PDX Collection 1063:31 codes |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
P293 | Persistent fetal circulation |
Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
Q238 | Other congenital malformations of aortic and mitral valves |
Q239 | Congenital malformation of aortic and mitral valves, unspecified |
Q242 | Cor triatriatum |
Q243 | Pulmonary infundibular stenosis |
Q244 | Congenital subaortic stenosis |
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 |
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 1064:6 codes |
Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
Q238 | Other congenital malformations of aortic and mitral valves |
Q239 | Congenital malformation of aortic and mitral valves, unspecified |
Q245 | Malformation of coronary vessels |
Q248 | Other specified congenital malformations of heart |
Q249 | Congenital malformation of heart, unspecified |
|
PDX Collection 1065:29 codes |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
P293 | Persistent fetal circulation |
Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
Q238 | Other congenital malformations of aortic and mitral valves |
Q239 | Congenital malformation of aortic and mitral valves, unspecified |
Q246 | Congenital heart block |
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 |
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 1066:6 codes |
Q250 | Patent ductus arteriosus |
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 |
|
PDX Collection 1067:18 codes |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
Q251 | Coarctation of aorta |
Q252 | Atresia of aorta |
Q253 | Supravalvular aortic stenosis |
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 |
Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
Q897 | Multiple congenital malformations, not elsewhere classified |
Q898 | Other specified congenital malformations |
|
PDX Collection 1068:26 codes |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
P293 | Persistent fetal circulation |
Q251 | Coarctation of aorta |
Q252 | Atresia of aorta |
Q253 | Supravalvular aortic stenosis |
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 |
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 |