| 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 |