| PDX Collection 5436 (continued) |
| 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 5437 |
| 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 5438 |
| D7881 | Other intraoperative complications of the spleen |
| D7889 | Other postprocedural complications of the spleen |
| E368 | Other intraoperative complications of endocrine system |
| E89810 | Postprocedural hemorrhage of an endocrine system organ or structure following an endocrine system procedure |
| E89811 | Postprocedural hemorrhage of an endocrine system organ or structure following other procedure |
| E89820 | Postprocedural hematoma of an endocrine system organ or structure following an endocrine system procedure |
| E89821 | Postprocedural hematoma of an endocrine system organ or structure following other procedure |
| E89822 | Postprocedural seroma of an endocrine system organ or structure following an endocrine system procedure |
| E89823 | Postprocedural seroma of an endocrine system organ or structure following other procedure |
| E8989 | Other postprocedural endocrine and metabolic complications and disorders |
| H59011 | Keratopathy (bullous aphakic) following cataract surgery, right eye |
| H59012 | Keratopathy (bullous aphakic) following cataract surgery, left eye |
| H59013 | Keratopathy (bullous aphakic) following cataract surgery, bilateral |
| H59019 | Keratopathy (bullous aphakic) following cataract surgery, unspecified eye |
| H59031 | Cystoid macular edema following cataract surgery, right eye |
| H59032 | Cystoid macular edema following cataract surgery, left eye |
| H59033 | Cystoid macular edema following cataract surgery, bilateral |
| H59039 | Cystoid macular edema following cataract surgery, unspecified eye |
| H59091 | Other disorders of the right eye following cataract surgery |
| H59092 | Other disorders of the left eye following cataract surgery |
| H59093 | Other disorders of the eye following cataract surgery, bilateral |
| H59099 | Other disorders of unspecified eye following cataract surgery |
| H59811 | Chorioretinal scars after surgery for detachment, right eye |
| H59812 | Chorioretinal scars after surgery for detachment, left eye |
| H59813 | Chorioretinal scars after surgery for detachment, bilateral |
| H59819 | Chorioretinal scars after surgery for detachment, unspecified eye |
| H5988 | Other intraoperative complications of eye and adnexa, not elsewhere classified |
| H5989 | Other postprocedural complications and disorders of eye and adnexa, not elsewhere classified |
| H95811 | Postprocedural stenosis of right external ear canal |
| H95812 | Postprocedural stenosis of left external ear canal |
| H95813 | Postprocedural stenosis of external ear canal, bilateral |
| H95819 | Postprocedural stenosis of unspecified external ear canal |
| H9588 | Other intraoperative complications and disorders of the ear and mastoid process, not elsewhere classified |
| H9589 | Other postprocedural complications and disorders of the ear and mastoid process, not elsewhere classified |
| I973 | Postprocedural hypertension |
| J9587 | Transfusion-associated dyspnea (TAD) |
| L7681 | Other intraoperative complications of skin and subcutaneous tissue |
| L7682 | Other postprocedural complications of skin and subcutaneous tissue |
| M9689 | Other intraoperative and postprocedural complications and disorders of the musculoskeletal system |
| N981 | Hyperstimulation of ovaries |
| N982 | Complications of attempted introduction of fertilized ovum following in vitro fertilization |
| N983 | Complications of attempted introduction of embryo in embryo transfer |
| N988 | Other complications associated with artificial fertilization |
| N989 | Complication associated with artificial fertilization, unspecified |
| T81500A | Unspecified complication of foreign body accidentally left in body following surgical operation, initial encounter |
| T81501A | Unspecified complication of foreign body accidentally left in body following infusion or transfusion, initial encounter |
| T81502A | Unspecified complication of foreign body accidentally left in body following kidney dialysis, initial encounter |
| T81503A | Unspecified complication of foreign body accidentally left in body following injection or immunization, initial encounter |
| T81504A | Unspecified complication of foreign body accidentally left in body following endoscopic examination, initial encounter |
| T81505A | Unspecified complication of foreign body accidentally left in body following heart catheterization, initial encounter |
| T81506A | Unspecified complication of foreign body accidentally left in body following aspiration, puncture or other catheterization, initial encounter |
| T81507A | Unspecified complication of foreign body accidentally left in body following removal of catheter or packing, initial encounter |
| T81508A | Unspecified complication of foreign body accidentally left in body following other procedure, initial encounter |
| T81509A | Unspecified complication of foreign body accidentally left in body following unspecified procedure, initial encounter |
| T81510A | Adhesions due to foreign body accidentally left in body following surgical operation, initial encounter |
| T81511A | Adhesions due to foreign body accidentally left in body following infusion or transfusion, initial encounter |
| T81512A | Adhesions due to foreign body accidentally left in body following kidney dialysis, initial encounter |
| T81513A | Adhesions due to foreign body accidentally left in body following injection or immunization, initial encounter |
| T81514A | Adhesions due to foreign body accidentally left in body following endoscopic examination, initial encounter |
| T81515A | Adhesions due to foreign body accidentally left in body following heart catheterization, initial encounter |
| T81516A | Adhesions due to foreign body accidentally left in body following aspiration, puncture or other catheterization, initial encounter |
| T81517A | Adhesions due to foreign body accidentally left in body following removal of catheter or packing, initial encounter |
| T81518A | Adhesions due to foreign body accidentally left in body following other procedure, initial encounter |
| T81519A | Adhesions due to foreign body accidentally left in body following unspecified procedure, initial encounter |
| T81520A | Obstruction due to foreign body accidentally left in body following surgical operation, initial encounter |
| T81521A | Obstruction due to foreign body accidentally left in body following infusion or transfusion, initial encounter |
| T81522A | Obstruction due to foreign body accidentally left in body following kidney dialysis, initial encounter |
| T81523A | Obstruction due to foreign body accidentally left in body following injection or immunization, initial encounter |
| T81524A | Obstruction due to foreign body accidentally left in body following endoscopic examination, initial encounter |
| T81525A | Obstruction due to foreign body accidentally left in body following heart catheterization, initial encounter |
| T81526A | Obstruction due to foreign body accidentally left in body following aspiration, puncture or other catheterization, initial encounter |
| T81527A | Obstruction due to foreign body accidentally left in body following removal of catheter or packing, initial encounter |
| T81528A | Obstruction due to foreign body accidentally left in body following other procedure, initial encounter |
| T81529A | Obstruction due to foreign body accidentally left in body following unspecified procedure, initial encounter |
| T81530A | Perforation due to foreign body accidentally left in body following surgical operation, initial encounter |
| T81531A | Perforation due to foreign body accidentally left in body following infusion or transfusion, initial encounter |
| T81532A | Perforation due to foreign body accidentally left in body following kidney dialysis, initial encounter |
| T81533A | Perforation due to foreign body accidentally left in body following injection or immunization, initial encounter |
| T81534A | Perforation due to foreign body accidentally left in body following endoscopic examination, initial encounter |
| T81535A | Perforation due to foreign body accidentally left in body following heart catheterization, initial encounter |
| T81536A | Perforation due to foreign body accidentally left in body following aspiration, puncture or other catheterization, initial encounter |
| T81537A | Perforation due to foreign body accidentally left in body following removal of catheter or packing, initial encounter |
| T81538A | Perforation due to foreign body accidentally left in body following other procedure, initial encounter |
| T81539A | Perforation due to foreign body accidentally left in body following unspecified procedure, initial encounter |
| T81590A | Other complications of foreign body accidentally left in body following surgical operation, initial encounter |
| T81591A | Other complications of foreign body accidentally left in body following infusion or transfusion, initial encounter |
| T81592A | Other complications of foreign body accidentally left in body following kidney dialysis, initial encounter |
| T81593A | Other complications of foreign body accidentally left in body following injection or immunization, initial encounter |
| T81594A | Other complications of foreign body accidentally left in body following endoscopic examination, initial encounter |
| T81595A | Other complications of foreign body accidentally left in body following heart catheterization, initial encounter |
| T81596A | Other complications of foreign body accidentally left in body following aspiration, puncture or other catheterization, initial encounter |
| T81597A | Other complications of foreign body accidentally left in body following removal of catheter or packing, initial encounter |
| T81598A | Other complications of foreign body accidentally left in body following other procedure, initial encounter |
| T81599A | Other complications of foreign body accidentally left in body following unspecified procedure, initial encounter |
| T8182XA | Emphysema (subcutaneous) resulting from a procedure, initial encounter |
| T8189XA | Other complications of procedures, not elsewhere classified, initial encounter |
| T819XXA | Unspecified complication of procedure, initial encounter |
| |
| PDX Collection 5439 |
| 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 5440 |
| 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 5441 |
| D800 | Hereditary hypogammaglobulinemia |
| D803 | Selective deficiency of immunoglobulin G [IgG] subclasses |
| D804 | Selective deficiency of immunoglobulin M [IgM] |
| D805 | Immunodeficiency with increased immunoglobulin M [IgM] |
| D806 | Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia |
| D807 | Transient hypogammaglobulinemia of infancy |
| D808 | Other immunodeficiencies with predominantly antibody defects |
| D809 | Immunodeficiency with predominantly antibody defects, unspecified |
| D810 | Severe combined immunodeficiency [SCID] with reticular dysgenesis |
| D811 | Severe combined immunodeficiency [SCID] with low T- and B-cell numbers |
| D812 | Severe combined immunodeficiency [SCID] with low or normal B-cell numbers |
| D814 | Nezelof's syndrome |
| D816 | Major histocompatibility complex class I deficiency |
| D817 | Major histocompatibility complex class II deficiency |
| D8182 | Activated Phosphoinositide 3-kinase Delta Syndrome [APDS] |
| D8189 | Other combined immunodeficiencies |
| D819 | Combined immunodeficiency, unspecified |
| D820 | Wiskott-Aldrich syndrome |
| D821 | Di George's syndrome |
| D822 | Immunodeficiency with short-limbed stature |
| D823 | Immunodeficiency following hereditary defective response to Epstein-Barr virus |
| D824 | Hyperimmunoglobulin E [IgE] syndrome |
| D828 | Immunodeficiency associated with other specified major defects |
| D829 | Immunodeficiency associated with major defect, unspecified |
| D830 | Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function |
| D831 | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders |
| D832 | Common variable immunodeficiency with autoantibodies to B- or T-cells |
| D838 | Other common variable immunodeficiencies |
| D839 | Common variable immunodeficiency, unspecified |
| D840 | Lymphocyte function antigen-1 [LFA-1] defect |
| D8481 | Immunodeficiency due to conditions classified elsewhere |
| D84821 | Immunodeficiency due to drugs |
| D84822 | Immunodeficiency due to external causes |
| D8489 | Other immunodeficiencies |
| D849 | Immunodeficiency, unspecified |
| D893 | Immune reconstitution syndrome |
| D8940 | Mast cell activation, unspecified |
| D8941 | Monoclonal mast cell activation syndrome |
| D8942 | Idiopathic mast cell activation syndrome |
| D8943 | Secondary mast cell activation |
| D8949 | Other mast cell activation disorder |
| D8982 | Autoimmune lymphoproliferative syndrome [ALPS] |
| D8989 | Other specified disorders involving the immune mechanism, not elsewhere classified |
| D899 | Disorder involving the immune mechanism, unspecified |
| |
| PDX Collection 5442 |
| E7871 | Barth syndrome |
| E7872 | Smith-Lemli-Opitz syndrome |
| Q8581 | PTEN tumor syndrome |
| Q8582 | Other Cowden syndrome |
| Q8583 | Von Hippel-Lindau syndrome |
| Q8589 | Other phakomatoses, not elsewhere classified |
| Q859 | Phakomatosis, 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'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 |
| Q899 | Congenital malformation, unspecified |
| Q992 | Fragile X chromosome |
| |
| PDX Collection 5443 |
| E7871 | Barth syndrome |
| E7872 | Smith-Lemli-Opitz syndrome |
| Q8581 | PTEN tumor syndrome |
| Q8582 | Other Cowden syndrome |
| Q8583 | Von Hippel-Lindau syndrome |
| Q8589 | Other phakomatoses, not elsewhere classified |
| Q859 | Phakomatosis, 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'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 |
| Q899 | Congenital malformation, unspecified |
| Q992 | Fragile X chromosome |
| |
| PDX Collection 5444 |
| E7871 | Barth syndrome |
| E7872 | Smith-Lemli-Opitz syndrome |
| Q8581 | PTEN tumor syndrome |
| Q8582 | Other Cowden syndrome |
| Q8583 | Von Hippel-Lindau syndrome |
| Q8589 | Other phakomatoses, not elsewhere classified |
| Q859 | Phakomatosis, 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'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 |
| Q899 | Congenital malformation, unspecified |
| Q992 | Fragile X chromosome |
| |
| PDX Collection 5445 |
| S0190XA | Unspecified open wound of unspecified part of head, initial encounter |
| S0191XA | Laceration without foreign body of unspecified part of head, initial encounter |
| S0192XA | Laceration with foreign body of unspecified part of head, initial encounter |
| S0193XA | Puncture wound without foreign body of unspecified part of head, initial encounter |
| S0194XA | Puncture wound with foreign body of unspecified part of head, initial encounter |
| S0195XA | Open bite of unspecified part of head, initial encounter |
| S020XXA | Fracture of vault of skull, initial encounter for closed fracture |
| S020XXB | Fracture of vault of skull, initial encounter for open fracture |
| S020XXS | Fracture of vault of skull, sequela |
| S02101A | Fracture of base of skull, right side, initial encounter for closed fracture |
| S02101B | Fracture of base of skull, right side, initial encounter for open fracture |
| S02101S | Fracture of base of skull, right side, sequela |
| S02102A | Fracture of base of skull, left side, initial encounter for closed fracture |
| S02102B | Fracture of base of skull, left side, initial encounter for open fracture |
| S02102S | Fracture of base of skull, left side, sequela |
| S02109A | Fracture of base of skull, unspecified side, initial encounter for closed fracture |
| S02109B | Fracture of base of skull, unspecified side, initial encounter for open fracture |
| S02109S | Fracture of base of skull, unspecified side, sequela |
| S02110A | Type I occipital condyle fracture, unspecified side, initial encounter for closed fracture |
| S02110B | Type I occipital condyle fracture, unspecified side, initial encounter for open fracture |
![Previous Page [Alt-p]](bakpg.png){kind=small}
![Up a level [Alt-u]](uptop.png){kind=small}
![Next Page [Alt-n]](fwdpg.png){kind=small}