| PDX Collection 6188 (continued) |
| N1419 | Nephropathy induced by other drugs, medicaments and biological substances |
| N142 | Nephropathy induced by unspecified drug, medicament or biological substance |
| N143 | Nephropathy induced by heavy metals |
| N144 | Toxic nephropathy, not elsewhere classified |
| N150 | Balkan nephropathy |
| N151 | Renal and perinephric abscess |
| N158 | Other specified renal tubulo-interstitial diseases |
| N159 | Renal tubulo-interstitial disease, unspecified |
| N170 | Acute kidney failure with tubular necrosis |
| N171 | Acute kidney failure with acute cortical necrosis |
| N172 | Acute kidney failure with medullary necrosis |
| N178 | Other acute kidney failure |
| N179 | Acute kidney failure, unspecified |
| N19 | Unspecified kidney failure |
| N250 | Renal osteodystrophy |
| N251 | Nephrogenic diabetes insipidus |
| N2581 | Secondary hyperparathyroidism of renal origin |
| N2589 | Other disorders resulting from impaired renal tubular function |
| N259 | Disorder resulting from impaired renal tubular function, unspecified |
| N261 | Atrophy of kidney (terminal) |
| N269 | Renal sclerosis, unspecified |
| N270 | Small kidney, unilateral |
| N271 | Small kidney, bilateral |
| N279 | Small kidney, unspecified |
| N281 | Cyst of kidney, acquired |
| N2881 | Hypertrophy of kidney |
| N2882 | Megaloureter |
| N2883 | Nephroptosis |
| N2884 | Pyelitis cystica |
| N2885 | Pyeloureteritis cystica |
| N2886 | Ureteritis cystica |
| N2889 | Other specified disorders of kidney and ureter |
| N289 | Disorder of kidney and ureter, unspecified |
| N3641 | Hypermobility of urethra |
| N3642 | Intrinsic sphincter deficiency (ISD) |
| N3643 | Combined hypermobility of urethra and intrinsic sphincter deficiency |
| N368 | Other specified disorders of urethra |
| N369 | Urethral disorder, unspecified |
| N398 | Other specified disorders of urinary system |
| N399 | Disorder of urinary system, unspecified |
| N80A0 | Endometriosis of bladder, unspecified depth |
| N80A1 | Superficial endometriosis of bladder |
| N80A2 | Deep endometriosis of bladder |
| N80A41 | Superficial endometriosis of right ureter |
| N80A42 | Superficial endometriosis of left ureter |
| N80A43 | Superficial endometriosis of bilateral ureters |
| N80A49 | Superficial endometriosis of unspecified ureter |
| N80A51 | Deep endometriosis of right ureter |
| N80A52 | Deep endometriosis of left ureter |
| N80A53 | Deep endometriosis of bilateral ureters |
| N80A59 | Deep endometriosis of unspecified ureter |
| N80A61 | Endometriosis of right ureter, unspecified depth |
| N80A62 | Endometriosis of left ureter, unspecified depth |
| N80A63 | Endometriosis of bilateral ureters, unspecified depth |
| N80A69 | Endometriosis of unspecified ureter, unspecified depth |
| R310 | Gross hematuria |
| R311 | Benign essential microscopic hematuria |
| R3121 | Asymptomatic microscopic hematuria |
| R3129 | Other microscopic hematuria |
| R319 | Hematuria, unspecified |
| |
| PDX Collection 6189 |
| K634 | Enteroptosis |
| K638211 | Small intestinal bacterial overgrowth, hydrogen-subtype |
| K638212 | Small intestinal bacterial overgrowth, hydrogen sulfide-subtype |
| K638219 | Small intestinal bacterial overgrowth, unspecified |
| K63822 | Small intestinal fungal overgrowth |
| K63829 | Intestinal methanogen overgrowth, unspecified |
| K6389 | Other specified diseases of intestine |
| K639 | Disease of intestine, unspecified |
| K650 | Generalized (acute) peritonitis |
| K651 | Peritoneal abscess |
| K652 | Spontaneous bacterial peritonitis |
| K653 | Choleperitonitis |
| K654 | Sclerosing mesenteritis |
| K658 | Other peritonitis |
| K659 | Peritonitis, unspecified |
| K6819 | Other retroperitoneal abscess |
| K682 | Retroperitoneal fibrosis |
| K683 | Retroperitoneal hematoma |
| K689 | Other disorders of retroperitoneum |
| K9289 | Other specified diseases of the digestive system |
| K929 | Disease of digestive system, unspecified |
| R1113 | Vomiting of fecal matter |
| |
| PDX Collection 6190 |
| 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 |
| I234 | Rupture of chordae tendineae as current complication following acute myocardial infarction |
| I235 | Rupture of papillary muscle 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 |
| I400 | Infective myocarditis |
| I401 | Isolated myocarditis |
| I408 | Other acute myocarditis |
| I409 | Acute myocarditis, unspecified |
| I510 | Cardiac septal defect, acquired |
| I511 | Rupture of chordae tendineae, not elsewhere classified |
| I512 | Rupture of papillary muscle, not elsewhere classified |
| I514 | Myocarditis, unspecified |
| I878 | Other specified disorders of veins |
| I879 | Disorder of vein, unspecified |
| I970 | Postcardiotomy syndrome |
| I97110 | Postprocedural cardiac insufficiency following cardiac surgery |
| I97111 | Postprocedural cardiac insufficiency following other surgery |
| I97120 | Postprocedural cardiac arrest following cardiac surgery |
| I97121 | Postprocedural cardiac arrest following other surgery |
| I97130 | Postprocedural heart failure following cardiac surgery |
| I97131 | Postprocedural heart failure following other surgery |
| I97190 | Other postprocedural cardiac functional disturbances following cardiac surgery |
| I97191 | Other postprocedural cardiac functional disturbances following other surgery |
| I998 | Other disorder of circulatory system |
| I999 | Unspecified disorder of circulatory system |
| P2930 | Pulmonary hypertension of newborn |
| P2938 | Other persistent fetal circulation |
| Q200 | Common arterial trunk |
| Q201 | Double outlet right ventricle |
| Q202 | Double outlet left ventricle |
| Q203 | Discordant ventriculoarterial connection |
| Q204 | Double inlet ventricle |
| Q205 | Discordant atrioventricular connection |
| Q206 | Isomerism of atrial appendages |
| Q208 | Other congenital malformations of cardiac chambers and connections |
| Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
| Q210 | Ventricular septal defect |
| Q2110 | Atrial septal defect, unspecified |
| Q2111 | Secundum atrial septal defect |
| Q2112 | Patent foramen ovale |
| Q2113 | Coronary sinus atrial septal defect |
| Q2114 | Superior sinus venosus atrial septal defect |
| Q2115 | Inferior sinus venosus atrial septal defect |
| Q2116 | Sinus venosus atrial septal defect, unspecified |
| Q2119 | Other specified atrial septal defect |
| Q2120 | Atrioventricular septal defect, unspecified as to partial or complete |
| Q2121 | Partial atrioventricular septal defect |
| Q2122 | Transitional atrioventricular septal defect |
| Q2123 | Complete atrioventricular septal defect |
| Q213 | Tetralogy of Fallot |
| Q214 | Aortopulmonary septal defect |
| Q218 | Other congenital malformations of cardiac septa |
| Q219 | Congenital malformation of cardiac septum, unspecified |
| Q238 | Other congenital malformations of aortic and mitral valves |
| Q239 | Congenital malformation of aortic and mitral valves, unspecified |
| Q248 | Other specified congenital malformations of heart |
| Q249 | Congenital malformation of heart, unspecified |
| Q2730 | Arteriovenous malformation, site unspecified |
| Q274 | Congenital phlebectasia |
| Q280 | Arteriovenous malformation of precerebral vessels |
| Q281 | Other malformations of precerebral vessels |
| Q288 | Other specified congenital malformations of circulatory system |
| Q289 | Congenital malformation of circulatory system, unspecified |
| Q8711 | Prader-Willi syndrome |
| Q8719 | Other congenital malformation syndromes predominantly associated with short stature |
| Q872 | Congenital malformation syndromes predominantly involving limbs |
| Q873 | Congenital malformation syndromes involving early overgrowth |
| Q8740 | Marfan syndrome, unspecified |
| Q87410 | Marfan syndrome with aortic dilation |
| Q87418 | Marfan syndrome with other cardiovascular manifestations |
| Q8742 | Marfan syndrome with ocular manifestations |
| Q8743 | Marfan syndrome with skeletal manifestation |
| Q875 | Other congenital malformation syndromes with other skeletal changes |
| Q8781 | Alport syndrome |
| Q8782 | Arterial tortuosity syndrome |
| Q8783 | Bardet-Biedl syndrome |
| Q8784 | Laurence-Moon syndrome |
| Q8785 | MED13L syndrome |
| Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
| Q897 | Multiple congenital malformations, not elsewhere classified |
| Q898 | Other specified congenital malformations |
| Q992 | Fragile X chromosome |
| |
| PDX Collection 6191 |
| K634 | Enteroptosis |
| K638211 | Small intestinal bacterial overgrowth, hydrogen-subtype |
| K638212 | Small intestinal bacterial overgrowth, hydrogen sulfide-subtype |
| K638219 | Small intestinal bacterial overgrowth, unspecified |
| K63822 | Small intestinal fungal overgrowth |
| K63829 | Intestinal methanogen overgrowth, unspecified |
| K6389 | Other specified diseases of intestine |
| K639 | Disease of intestine, unspecified |
| K650 | Generalized (acute) peritonitis |
| K651 | Peritoneal abscess |
| K652 | Spontaneous bacterial peritonitis |
| K653 | Choleperitonitis |
| K654 | Sclerosing mesenteritis |
| K658 | Other peritonitis |
| K659 | Peritonitis, unspecified |
| K6819 | Other retroperitoneal abscess |
| K682 | Retroperitoneal fibrosis |
| K683 | Retroperitoneal hematoma |
| K689 | Other disorders of retroperitoneum |
| K9289 | Other specified diseases of the digestive system |
| K929 | Disease of digestive system, unspecified |
| R1113 | Vomiting of fecal matter |
| |
| PDX Collection 6192 |
| 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 |
| I234 | Rupture of chordae tendineae as current complication following acute myocardial infarction |
| I235 | Rupture of papillary muscle 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 |
| I400 | Infective myocarditis |
| I401 | Isolated myocarditis |
| I408 | Other acute myocarditis |
| I409 | Acute myocarditis, unspecified |
| I510 | Cardiac septal defect, acquired |
| I511 | Rupture of chordae tendineae, not elsewhere classified |
| I512 | Rupture of papillary muscle, not elsewhere classified |
| I514 | Myocarditis, unspecified |
| I878 | Other specified disorders of veins |
| I879 | Disorder of vein, unspecified |
| I970 | Postcardiotomy syndrome |
| I97110 | Postprocedural cardiac insufficiency following cardiac surgery |
| I97111 | Postprocedural cardiac insufficiency following other surgery |
| I97120 | Postprocedural cardiac arrest following cardiac surgery |
| I97121 | Postprocedural cardiac arrest following other surgery |
| I97130 | Postprocedural heart failure following cardiac surgery |
| I97131 | Postprocedural heart failure following other surgery |
| I97190 | Other postprocedural cardiac functional disturbances following cardiac surgery |
| I97191 | Other postprocedural cardiac functional disturbances following other surgery |
| I998 | Other disorder of circulatory system |
| I999 | Unspecified disorder of circulatory system |
| P2930 | Pulmonary hypertension of newborn |
| P2938 | Other persistent fetal circulation |
| Q200 | Common arterial trunk |
| Q201 | Double outlet right ventricle |
| Q202 | Double outlet left ventricle |
| Q203 | Discordant ventriculoarterial connection |
| Q204 | Double inlet ventricle |
| Q205 | Discordant atrioventricular connection |
| Q206 | Isomerism of atrial appendages |
| Q208 | Other congenital malformations of cardiac chambers and connections |
| Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
| Q210 | Ventricular septal defect |
| Q2110 | Atrial septal defect, unspecified |
| Q2111 | Secundum atrial septal defect |
| Q2112 | Patent foramen ovale |
| Q2113 | Coronary sinus atrial septal defect |
| Q2114 | Superior sinus venosus atrial septal defect |
| Q2115 | Inferior sinus venosus atrial septal defect |
| Q2116 | Sinus venosus atrial septal defect, unspecified |
| Q2119 | Other specified atrial septal defect |
| Q2120 | Atrioventricular septal defect, unspecified as to partial or complete |
| Q2121 | Partial atrioventricular septal defect |
| Q2122 | Transitional atrioventricular septal defect |
| Q2123 | Complete atrioventricular septal defect |
| Q213 | Tetralogy of Fallot |
| Q214 | Aortopulmonary septal defect |
| Q218 | Other congenital malformations of cardiac septa |
| Q219 | Congenital malformation of cardiac septum, unspecified |
| Q238 | Other congenital malformations of aortic and mitral valves |
| Q239 | Congenital malformation of aortic and mitral valves, unspecified |
| Q248 | Other specified congenital malformations of heart |
| Q249 | Congenital malformation of heart, unspecified |
| Q2730 | Arteriovenous malformation, site unspecified |
| Q274 | Congenital phlebectasia |
| Q280 | Arteriovenous malformation of precerebral vessels |
| Q281 | Other malformations of precerebral vessels |
| Q288 | Other specified congenital malformations of circulatory system |
| Q289 | Congenital malformation of circulatory system, unspecified |
| Q8711 | Prader-Willi syndrome |
| Q8719 | Other congenital malformation syndromes predominantly associated with short stature |
| Q872 | Congenital malformation syndromes predominantly involving limbs |
| Q873 | Congenital malformation syndromes involving early overgrowth |
| Q8740 | Marfan syndrome, unspecified |
| Q87410 | Marfan syndrome with aortic dilation |
| Q87418 | Marfan syndrome with other cardiovascular manifestations |
| Q8742 | Marfan syndrome with ocular manifestations |
| Q8743 | Marfan syndrome with skeletal manifestation |
| Q875 | Other congenital malformation syndromes with other skeletal changes |
| Q8781 | Alport syndrome |
| Q8782 | Arterial tortuosity syndrome |
| Q8783 | Bardet-Biedl syndrome |
| Q8784 | Laurence-Moon syndrome |
| Q8785 | MED13L syndrome |
| Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
| Q897 | Multiple congenital malformations, not elsewhere classified |
| Q898 | Other specified congenital malformations |
| Q992 | Fragile X chromosome |
| |
| PDX Collection 6193 |
| 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 |
| I234 | Rupture of chordae tendineae as current complication following acute myocardial infarction |
| I235 | Rupture of papillary muscle 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 |
| I400 | Infective myocarditis |
| I401 | Isolated myocarditis |
| I408 | Other acute myocarditis |
| I409 | Acute myocarditis, unspecified |
| I510 | Cardiac septal defect, acquired |
| I511 | Rupture of chordae tendineae, not elsewhere classified |
| I512 | Rupture of papillary muscle, not elsewhere classified |
| I514 | Myocarditis, unspecified |
| I878 | Other specified disorders of veins |
| I879 | Disorder of vein, unspecified |
| I970 | Postcardiotomy syndrome |
| I97110 | Postprocedural cardiac insufficiency following cardiac surgery |
| I97111 | Postprocedural cardiac insufficiency following other surgery |
| I97120 | Postprocedural cardiac arrest following cardiac surgery |
| I97121 | Postprocedural cardiac arrest following other surgery |
| I97130 | Postprocedural heart failure following cardiac surgery |
| I97131 | Postprocedural heart failure following other surgery |
| I97190 | Other postprocedural cardiac functional disturbances following cardiac surgery |
| I97191 | Other postprocedural cardiac functional disturbances following other surgery |
| I998 | Other disorder of circulatory system |
| I999 | Unspecified disorder of circulatory system |
| P2930 | Pulmonary hypertension of newborn |
| P2938 | Other persistent fetal circulation |
| Q200 | Common arterial trunk |
| Q201 | Double outlet right ventricle |
| Q202 | Double outlet left ventricle |
| Q203 | Discordant ventriculoarterial connection |
| Q204 | Double inlet ventricle |
| Q205 | Discordant atrioventricular connection |
| Q206 | Isomerism of atrial appendages |
| Q208 | Other congenital malformations of cardiac chambers and connections |
| Q209 | Congenital malformation of cardiac chambers and connections, unspecified |
| Q210 | Ventricular septal defect |
| Q2110 | Atrial septal defect, unspecified |
| Q2111 | Secundum atrial septal defect |
| Q2112 | Patent foramen ovale |
| Q2113 | Coronary sinus atrial septal defect |
| Q2114 | Superior sinus venosus atrial septal defect |
| Q2115 | Inferior sinus venosus atrial septal defect |
| Q2116 | Sinus venosus atrial septal defect, unspecified |
| Q2119 | Other specified atrial septal defect |
| Q2120 | Atrioventricular septal defect, unspecified as to partial or complete |
| Q2121 | Partial atrioventricular septal defect |
| Q2122 | Transitional atrioventricular septal defect |
| Q2123 | Complete atrioventricular septal defect |
| Q213 | Tetralogy of Fallot |
| Q214 | Aortopulmonary septal defect |
| Q218 | Other congenital malformations of cardiac septa |
| Q219 | Congenital malformation of cardiac septum, unspecified |
| Q238 | Other congenital malformations of aortic and mitral valves |
| Q239 | Congenital malformation of aortic and mitral valves, unspecified |
| Q248 | Other specified congenital malformations of heart |
| Q249 | Congenital malformation of heart, unspecified |
| Q2730 | Arteriovenous malformation, site unspecified |
| Q274 | Congenital phlebectasia |
| Q280 | Arteriovenous malformation of precerebral vessels |
| Q281 | Other malformations of precerebral vessels |
| Q288 | Other specified congenital malformations of circulatory system |
| Q289 | Congenital malformation of circulatory system, unspecified |
| Q8711 | Prader-Willi syndrome |
| Q8719 | Other congenital malformation syndromes predominantly associated with short stature |
| Q872 | Congenital malformation syndromes predominantly involving limbs |
| Q873 | Congenital malformation syndromes involving early overgrowth |
| Q8740 | Marfan syndrome, unspecified |
| Q87410 | Marfan syndrome with aortic dilation |
| Q87418 | Marfan syndrome with other cardiovascular manifestations |
| Q8742 | Marfan syndrome with ocular manifestations |
| Q8743 | Marfan syndrome with skeletal manifestation |
| Q875 | Other congenital malformation syndromes with other skeletal changes |
| Q8781 | Alport syndrome |
| Q8782 | Arterial tortuosity syndrome |
| Q8783 | Bardet-Biedl syndrome |
| Q8784 | Laurence-Moon syndrome |
| Q8785 | MED13L syndrome |
| Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
| Q897 | Multiple congenital malformations, not elsewhere classified |
| Q898 | Other specified congenital malformations |
| Q992 | Fragile X chromosome |
| |
| PDX Collection 6194 |
| A33 | Tetanus neonatorum |
| A35 | Other tetanus |
| G10 | Huntington's disease |
| G110 | Congenital nonprogressive ataxia |
| G1110 | Early-onset cerebellar ataxia, unspecified |
| G1111 | Friedreich ataxia |
| G1119 | Other early-onset cerebellar ataxia |
| G112 | Late-onset cerebellar ataxia |
| G114 | Hereditary spastic paraplegia |
| G20A1 | Parkinson's disease without dyskinesia, without mention of fluctuations |
| G20A2 | Parkinson's disease without dyskinesia, with fluctuations |
| G20B1 | Parkinson's disease with dyskinesia, without mention of fluctuations |
| G20B2 | Parkinson's disease with dyskinesia, with fluctuations |
| G20C | Parkinsonism, unspecified |
| G210 | Malignant neuroleptic syndrome |
| G2111 | Neuroleptic induced parkinsonism |
| G2119 | Other drug induced secondary parkinsonism |
| G212 | Secondary parkinsonism due to other external agents |
| G213 | Postencephalitic parkinsonism |
| G214 | Vascular parkinsonism |
| G218 | Other secondary parkinsonism |
| G219 | Secondary parkinsonism, unspecified |
| G230 | Hallervorden-Spatz disease |
| G231 | Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski] |
| G232 | Striatonigral degeneration |
| G233 | Hypomyelination with atrophy of the basal ganglia and cerebellum |
| G238 | Other specified degenerative diseases of basal ganglia |
| G239 | Degenerative disease of basal ganglia, unspecified |
| G2401 | Drug induced subacute dyskinesia |
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