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 |