|
PDX Collection 3437 |
S090XXA | Injury of blood vessels of head, not elsewhere classified, initial encounter |
S15101A | Unspecified injury of right vertebral artery, initial encounter |
S15102A | Unspecified injury of left vertebral artery, initial encounter |
S15109A | Unspecified injury of unspecified vertebral artery, initial encounter |
S15111A | Minor laceration of right vertebral artery, initial encounter |
S15112A | Minor laceration of left vertebral artery, initial encounter |
S15119A | Minor laceration of unspecified vertebral artery, initial encounter |
S15121A | Major laceration of right vertebral artery, initial encounter |
S15122A | Major laceration of left vertebral artery, initial encounter |
S15129A | Major laceration of unspecified vertebral artery, initial encounter |
S15191A | Other specified injury of right vertebral artery, initial encounter |
S15192A | Other specified injury of left vertebral artery, initial encounter |
S15199A | Other specified injury of unspecified vertebral artery, initial encounter |
S15399A | Other specified injury of unspecified internal jugular vein, initial encounter |
S158XXA | Injury of other specified blood vessels at neck level, initial encounter |
S159XXA | Injury of unspecified blood vessel at neck level, initial encounter |
T07XXXA | Unspecified multiple injuries, initial encounter |
T148XXA | Other injury of unspecified body region, initial encounter |
T1490XA | Injury, unspecified, initial encounter |
T1491XA | Suicide attempt, initial encounter |
T798XXA | Other early complications of trauma, initial encounter |
T799XXA | Unspecified early complication of trauma, initial encounter |
T79A0XA | Compartment syndrome, unspecified, initial encounter |
T79A11A | Traumatic compartment syndrome of right upper extremity, initial encounter |
T79A12A | Traumatic compartment syndrome of left upper extremity, initial encounter |
T79A19A | Traumatic compartment syndrome of unspecified upper extremity, initial encounter |
T79A21A | Traumatic compartment syndrome of right lower extremity, initial encounter |
T79A22A | Traumatic compartment syndrome of left lower extremity, initial encounter |
T79A29A | Traumatic compartment syndrome of unspecified lower extremity, initial encounter |
T79A3XA | Traumatic compartment syndrome of abdomen, initial encounter |
T79A9XA | Traumatic compartment syndrome of other sites, initial encounter |
|
PDX Collection 3453 |
D62 | Acute posthemorrhagic anemia |
D644 | Congenital dyserythropoietic anemia |
D6481 | Anemia due to antineoplastic chemotherapy |
D6489 | Other specified anemias |
D649 | Anemia, unspecified |
R710 | Precipitous drop in hematocrit |
|
PDX Collection 3454 |
Z1612 | Extended spectrum beta lactamase (ESBL) resistance |
|
PDX Collection 3455 |
Z1621 | Resistance to vancomycin |
|
PDX Collection 3456 |
Z1624 | Resistance to multiple antibiotics |
|
PDX Collection 3457 |
Z1639 | Resistance to other specified antimicrobial drug |
|
PDX Collection 3458 |
P700 | Syndrome of infant of mother with gestational diabetes |
P701 | Syndrome of infant of a diabetic mother |
P702 | Neonatal diabetes mellitus |
P703 | Iatrogenic neonatal hypoglycemia |
P704 | Other neonatal hypoglycemia |
P708 | Other transitory disorders of carbohydrate metabolism of newborn |
P709 | Transitory disorder of carbohydrate metabolism of newborn, unspecified |
P710 | Cow's milk hypocalcemia in newborn |
P711 | Other neonatal hypocalcemia |
P712 | Neonatal hypomagnesemia |
P713 | Neonatal tetany without calcium or magnesium deficiency |
P714 | Transitory neonatal hypoparathyroidism |
P718 | Other transitory neonatal disorders of calcium and magnesium metabolism |
P719 | Transitory neonatal disorder of calcium and magnesium metabolism, unspecified |
P721 | Transitory neonatal hyperthyroidism |
P729 | Transitory neonatal endocrine disorder, unspecified |
P740 | Late metabolic acidosis of newborn |
P741 | Dehydration of newborn |
P7421 | Hypernatremia of newborn |
P7422 | Hyponatremia of newborn |
P7431 | Hyperkalemia of newborn |
P7432 | Hypokalemia of newborn |
P7441 | Alkalosis of newborn |
P74421 | Hyperchloremia of newborn |
P74422 | Hypochloremia of newborn |
P7449 | Other transitory electrolyte disturbance of newborn |
P749 | Transitory metabolic disturbance of newborn, unspecified |
P940 | Transient neonatal myasthenia gravis |
|
PDX Collection 3459 |
P700 | Syndrome of infant of mother with gestational diabetes |
P701 | Syndrome of infant of a diabetic mother |
P702 | Neonatal diabetes mellitus |
P703 | Iatrogenic neonatal hypoglycemia |
P704 | Other neonatal hypoglycemia |
P709 | Transitory disorder of carbohydrate metabolism of newborn, unspecified |
P710 | Cow's milk hypocalcemia in newborn |
P711 | Other neonatal hypocalcemia |
P712 | Neonatal hypomagnesemia |
P713 | Neonatal tetany without calcium or magnesium deficiency |
P714 | Transitory neonatal hypoparathyroidism |
P718 | Other transitory neonatal disorders of calcium and magnesium metabolism |
P719 | Transitory neonatal disorder of calcium and magnesium metabolism, unspecified |
P720 | Neonatal goiter, not elsewhere classified |
P721 | Transitory neonatal hyperthyroidism |
P729 | Transitory neonatal endocrine disorder, unspecified |
P740 | Late metabolic acidosis of newborn |
P741 | Dehydration of newborn |
P7421 | Hypernatremia of newborn |
P7422 | Hyponatremia of newborn |
P7431 | Hyperkalemia of newborn |
P7432 | Hypokalemia of newborn |
P7441 | Alkalosis of newborn |
P74421 | Hyperchloremia of newborn |
P74422 | Hypochloremia of newborn |
P7449 | Other transitory electrolyte disturbance of newborn |
P749 | Transitory metabolic disturbance of newborn, unspecified |
P940 | Transient neonatal myasthenia gravis |
|
PDX Collection 3460 |
P700 | Syndrome of infant of mother with gestational diabetes |
P701 | Syndrome of infant of a diabetic mother |
P702 | Neonatal diabetes mellitus |
P703 | Iatrogenic neonatal hypoglycemia |
P704 | Other neonatal hypoglycemia |
P709 | Transitory disorder of carbohydrate metabolism of newborn, unspecified |
P710 | Cow's milk hypocalcemia in newborn |
P711 | Other neonatal hypocalcemia |
P712 | Neonatal hypomagnesemia |
P713 | Neonatal tetany without calcium or magnesium deficiency |
P714 | Transitory neonatal hypoparathyroidism |
P718 | Other transitory neonatal disorders of calcium and magnesium metabolism |
P719 | Transitory neonatal disorder of calcium and magnesium metabolism, unspecified |
P721 | Transitory neonatal hyperthyroidism |
P722 | Other transitory neonatal disorders of thyroid function, not elsewhere classified |
P729 | Transitory neonatal endocrine disorder, unspecified |
P740 | Late metabolic acidosis of newborn |
P741 | Dehydration of newborn |
P7421 | Hypernatremia of newborn |
P7422 | Hyponatremia of newborn |
P7431 | Hyperkalemia of newborn |
P7432 | Hypokalemia of newborn |
P7441 | Alkalosis of newborn |
P74421 | Hyperchloremia of newborn |
P74422 | Hypochloremia of newborn |
P7449 | Other transitory electrolyte disturbance of newborn |
P749 | Transitory metabolic disturbance of newborn, unspecified |
P940 | Transient neonatal myasthenia gravis |
|
PDX Collection 3461 |
P700 | Syndrome of infant of mother with gestational diabetes |
P701 | Syndrome of infant of a diabetic mother |
P702 | Neonatal diabetes mellitus |
P703 | Iatrogenic neonatal hypoglycemia |
P704 | Other neonatal hypoglycemia |
P709 | Transitory disorder of carbohydrate metabolism of newborn, unspecified |
P710 | Cow's milk hypocalcemia in newborn |
P711 | Other neonatal hypocalcemia |
P712 | Neonatal hypomagnesemia |
P713 | Neonatal tetany without calcium or magnesium deficiency |
P714 | Transitory neonatal hypoparathyroidism |
P718 | Other transitory neonatal disorders of calcium and magnesium metabolism |
P719 | Transitory neonatal disorder of calcium and magnesium metabolism, unspecified |
P721 | Transitory neonatal hyperthyroidism |
P728 | Other specified transitory neonatal endocrine disorders |
P729 | Transitory neonatal endocrine disorder, unspecified |
P740 | Late metabolic acidosis of newborn |
P741 | Dehydration of newborn |
P7421 | Hypernatremia of newborn |
P7422 | Hyponatremia of newborn |
P7431 | Hyperkalemia of newborn |
P7432 | Hypokalemia of newborn |
P7441 | Alkalosis of newborn |
P74421 | Hyperchloremia of newborn |
P74422 | Hypochloremia of newborn |
P7449 | Other transitory electrolyte disturbance of newborn |
P749 | Transitory metabolic disturbance of newborn, unspecified |
P940 | Transient neonatal myasthenia gravis |
|
PDX Collection 3462 |
P700 | Syndrome of infant of mother with gestational diabetes |
P701 | Syndrome of infant of a diabetic mother |
P702 | Neonatal diabetes mellitus |
P703 | Iatrogenic neonatal hypoglycemia |
P704 | Other neonatal hypoglycemia |
P709 | Transitory disorder of carbohydrate metabolism of newborn, unspecified |
P710 | Cow's milk hypocalcemia in newborn |
P711 | Other neonatal hypocalcemia |
P712 | Neonatal hypomagnesemia |
P713 | Neonatal tetany without calcium or magnesium deficiency |
P714 | Transitory neonatal hypoparathyroidism |
P718 | Other transitory neonatal disorders of calcium and magnesium metabolism |
P719 | Transitory neonatal disorder of calcium and magnesium metabolism, unspecified |
P721 | Transitory neonatal hyperthyroidism |
P729 | Transitory neonatal endocrine disorder, unspecified |
P740 | Late metabolic acidosis of newborn |
P741 | Dehydration of newborn |
P7421 | Hypernatremia of newborn |
P7422 | Hyponatremia of newborn |
P7431 | Hyperkalemia of newborn |
P7432 | Hypokalemia of newborn |
P7441 | Alkalosis of newborn |
P74421 | Hyperchloremia of newborn |
P74422 | Hypochloremia of newborn |
P7449 | Other transitory electrolyte disturbance of newborn |
P745 | Transitory tyrosinemia of newborn |
P749 | Transitory metabolic disturbance of newborn, unspecified |
P940 | Transient neonatal myasthenia gravis |
|
PDX Collection 3463 |
P700 | Syndrome of infant of mother with gestational diabetes |
P701 | Syndrome of infant of a diabetic mother |
P702 | Neonatal diabetes mellitus |
P703 | Iatrogenic neonatal hypoglycemia |
P704 | Other neonatal hypoglycemia |
P709 | Transitory disorder of carbohydrate metabolism of newborn, unspecified |
P710 | Cow's milk hypocalcemia in newborn |
P711 | Other neonatal hypocalcemia |
P712 | Neonatal hypomagnesemia |
P713 | Neonatal tetany without calcium or magnesium deficiency |
P714 | Transitory neonatal hypoparathyroidism |
P718 | Other transitory neonatal disorders of calcium and magnesium metabolism |
P719 | Transitory neonatal disorder of calcium and magnesium metabolism, unspecified |
P721 | Transitory neonatal hyperthyroidism |
P729 | Transitory neonatal endocrine disorder, unspecified |
P740 | Late metabolic acidosis of newborn |
P741 | Dehydration of newborn |
P7421 | Hypernatremia of newborn |
P7422 | Hyponatremia of newborn |
P7431 | Hyperkalemia of newborn |
P7432 | Hypokalemia of newborn |
P7441 | Alkalosis of newborn |
P74421 | Hyperchloremia of newborn |
P74422 | Hypochloremia of newborn |
P7449 | Other transitory electrolyte disturbance of newborn |
P746 | Transitory hyperammonemia of newborn |
P749 | Transitory metabolic disturbance of newborn, unspecified |
P940 | Transient neonatal myasthenia gravis |
|
PDX Collection 3464 |
P700 | Syndrome of infant of mother with gestational diabetes |
P701 | Syndrome of infant of a diabetic mother |
P702 | Neonatal diabetes mellitus |
P703 | Iatrogenic neonatal hypoglycemia |
P704 | Other neonatal hypoglycemia |
P709 | Transitory disorder of carbohydrate metabolism of newborn, unspecified |
P710 | Cow's milk hypocalcemia in newborn |
P711 | Other neonatal hypocalcemia |
P712 | Neonatal hypomagnesemia |
P713 | Neonatal tetany without calcium or magnesium deficiency |
P714 | Transitory neonatal hypoparathyroidism |
P718 | Other transitory neonatal disorders of calcium and magnesium metabolism |
P719 | Transitory neonatal disorder of calcium and magnesium metabolism, unspecified |
P721 | Transitory neonatal hyperthyroidism |
P729 | Transitory neonatal endocrine disorder, unspecified |
P740 | Late metabolic acidosis of newborn |
P741 | Dehydration of newborn |
P7421 | Hypernatremia of newborn |
P7422 | Hyponatremia of newborn |
P7431 | Hyperkalemia of newborn |
P7432 | Hypokalemia of newborn |
P7441 | Alkalosis of newborn |
P74421 | Hyperchloremia of newborn |
P74422 | Hypochloremia of newborn |
P7449 | Other transitory electrolyte disturbance of newborn |
P748 | Other transitory metabolic disturbances of newborn |
P749 | Transitory metabolic disturbance of newborn, unspecified |
P940 | Transient neonatal myasthenia gravis |
|
PDX Collection 3467 |
Q7960 | Ehlers-Danlos syndrome, unspecified |
Q7961 | Classical Ehlers-Danlos syndrome |
Q7962 | Hypermobile Ehlers-Danlos syndrome |
Q7963 | Vascular Ehlers-Danlos syndrome |
Q7969 | Other Ehlers-Danlos syndromes |
|
PDX Collection 3485 |
Z1620 | Resistance to unspecified antibiotic |
|
PDX Collection 3486 |
Z1622 | Resistance to vancomycin related antibiotics |
|
PDX Collection 3487 |
Z1623 | Resistance to quinolones and fluoroquinolones |
|
PDX Collection 3488 |
Z1629 | Resistance to other single specified antibiotic |
|
PDX Collection 3489 |
Z1630 | Resistance to unspecified antimicrobial drugs |
|
PDX Collection 3490 |
Z1631 | Resistance to antiparasitic drug(s) |
|
PDX Collection 3491 |
Z1632 | Resistance to antifungal drug(s) |
|
PDX Collection 3492 |
Z1633 | Resistance to antiviral drug(s) |
|
PDX Collection 3493 |
Z16341 | Resistance to single antimycobacterial drug |
|
PDX Collection 3494 |
Z16342 | Resistance to multiple antimycobacterial drugs |
|
PDX Collection 3495 |
Z1635 | Resistance to multiple antimicrobial drugs |
|
PDX Collection 3496 |
Z1610 | Resistance to unspecified beta lactam antibiotics |
|
PDX Collection 3497 |
Z1611 | Resistance to penicillins |
|
PDX Collection 3498 |
Z1619 | Resistance to other specified beta lactam antibiotics |
|
PDX Collection 3499 |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
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 |
Q898 | Other specified congenital malformations |
Q992 | Fragile X chromosome |
|
PDX Collection 3500 |
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 |
I41 | Myocarditis in diseases classified elsewhere |
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 |
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 |
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 |
Q992 | Fragile X chromosome |
|
PDX Collection 3501 |
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 |
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 |
Q992 | Fragile X chromosome |
|
PDX Collection 3502 |
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 |
P2930 | Pulmonary hypertension of newborn |