| PDX Collection 1460 (continued) |
| P745 | Transitory tyrosinemia of newborn |
| P749 | Transitory metabolic disturbance of newborn, unspecified |
| P940 | Transient neonatal myasthenia gravis |
| |
| PDX Collection 1461 |
| 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 1462 |
| 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 1463 |
| P760 | Meconium plug syndrome |
| P761 | Transitory ileus of newborn |
| P762 | Intestinal obstruction due to inspissated milk |
| P768 | Other specified intestinal obstruction of newborn |
| P769 | Intestinal obstruction of newborn, unspecified |
| P771 | Stage 1 necrotizing enterocolitis in newborn |
| P772 | Stage 2 necrotizing enterocolitis in newborn |
| P773 | Stage 3 necrotizing enterocolitis in newborn |
| P779 | Necrotizing enterocolitis in newborn, unspecified |
| P780 | Perinatal intestinal perforation |
| P781 | Other neonatal peritonitis |
| P782 | Neonatal hematemesis and melena due to swallowed maternal blood |
| P783 | Noninfective neonatal diarrhea |
| P7881 | Congenital cirrhosis (of liver) |
| P7882 | Peptic ulcer of newborn |
| P7883 | Newborn esophageal reflux |
| P7884 | Gestational alloimmune liver disease |
| P7889 | Other specified perinatal digestive system disorders |
| P789 | Perinatal digestive system disorder, unspecified |
| |
| PDX Collection 1464 |
| P290 | Neonatal cardiac failure |
| P2911 | Neonatal tachycardia |
| P2912 | Neonatal bradycardia |
| P292 | Neonatal hypertension |
| P294 | Transient myocardial ischemia in newborn |
| P2989 | Other cardiovascular disorders originating in the perinatal period |
| P299 | Cardiovascular disorder originating in the perinatal period, unspecified |
| P760 | Meconium plug syndrome |
| P761 | Transitory ileus of newborn |
| P762 | Intestinal obstruction due to inspissated milk |
| P768 | Other specified intestinal obstruction of newborn |
| P769 | Intestinal obstruction of newborn, unspecified |
| P771 | Stage 1 necrotizing enterocolitis in newborn |
| P772 | Stage 2 necrotizing enterocolitis in newborn |
| P773 | Stage 3 necrotizing enterocolitis in newborn |
| P779 | Necrotizing enterocolitis in newborn, unspecified |
| P780 | Perinatal intestinal perforation |
| P781 | Other neonatal peritonitis |
| P782 | Neonatal hematemesis and melena due to swallowed maternal blood |
| P783 | Noninfective neonatal diarrhea |
| P7881 | Congenital cirrhosis (of liver) |
| P7882 | Peptic ulcer of newborn |
| P7883 | Newborn esophageal reflux |
| P7884 | Gestational alloimmune liver disease |
| P7889 | Other specified perinatal digestive system disorders |
| P789 | Perinatal digestive system disorder, unspecified |
| P941 | Congenital hypertonia |
| P942 | Congenital hypotonia |
| P948 | Other disorders of muscle tone of newborn |
| P949 | Disorder of muscle tone of newborn, unspecified |
| P960 | Congenital renal failure |
| P963 | Wide cranial sutures of newborn |
| P965 | Complication to newborn due to (fetal) intrauterine procedure |
| P9682 | Delayed separation of umbilical cord |
| P9683 | Meconium staining |
| P9689 | Other specified conditions originating in the perinatal period |
| |
| PDX Collection 1465 |
| P830 | Sclerema neonatorum |
| P8330 | Unspecified edema specific to newborn |
| P8339 | Other edema specific to newborn |
| |
| PDX Collection 1466 |
| P290 | Neonatal cardiac failure |
| P2911 | Neonatal tachycardia |
| P2912 | Neonatal bradycardia |
| P292 | Neonatal hypertension |
| P294 | Transient myocardial ischemia in newborn |
| P2989 | Other cardiovascular disorders originating in the perinatal period |
| P299 | Cardiovascular disorder originating in the perinatal period, unspecified |
| P832 | Hydrops fetalis not due to hemolytic disease |
| P941 | Congenital hypertonia |
| P942 | Congenital hypotonia |
| P948 | Other disorders of muscle tone of newborn |
| P949 | Disorder of muscle tone of newborn, unspecified |
| P960 | Congenital renal failure |
| P963 | Wide cranial sutures of newborn |
| P965 | Complication to newborn due to (fetal) intrauterine procedure |
| P9682 | Delayed separation of umbilical cord |
| P9683 | Meconium staining |
| P9689 | Other specified conditions originating in the perinatal period |
| |
| PDX Collection 1467 |
| P800 | Cold injury syndrome |
| P808 | Other hypothermia of newborn |
| P809 | Hypothermia of newborn, unspecified |
| P810 | Environmental hyperthermia of newborn |
| P818 | Other specified disturbances of temperature regulation of newborn |
| P819 | Disturbance of temperature regulation of newborn, unspecified |
| P830 | Sclerema neonatorum |
| P8330 | Unspecified edema specific to newborn |
| P8339 | Other edema specific to newborn |
| |
| PDX Collection 1468 |
| P290 | Neonatal cardiac failure |
| P2911 | Neonatal tachycardia |
| P2912 | Neonatal bradycardia |
| P292 | Neonatal hypertension |
| P294 | Transient myocardial ischemia in newborn |
| P2989 | Other cardiovascular disorders originating in the perinatal period |
| P299 | Cardiovascular disorder originating in the perinatal period, unspecified |
| P90 | Convulsions of newborn |
| P91819 | Neonatal encephalopathy, unspecified |
| P91821 | Neonatal cerebral infarction, right side of brain |
| P91822 | Neonatal cerebral infarction, left side of brain |
| P91823 | Neonatal cerebral infarction, bilateral |
| P91829 | Neonatal cerebral infarction, unspecified side |
| P9188 | Other specified disturbances of cerebral status of newborn |
| P919 | Disturbance of cerebral status of newborn, unspecified |
| P941 | Congenital hypertonia |
| P942 | Congenital hypotonia |
| P948 | Other disorders of muscle tone of newborn |
| P949 | Disorder of muscle tone of newborn, unspecified |
| P960 | Congenital renal failure |
| P963 | Wide cranial sutures of newborn |
| P965 | Complication to newborn due to (fetal) intrauterine procedure |
| P9682 | Delayed separation of umbilical cord |
| P9683 | Meconium staining |
| P9689 | Other specified conditions originating in the perinatal period |
| |
| PDX Collection 1469 |
| P90 | Convulsions of newborn |
| P910 | Neonatal cerebral ischemia |
| P911 | Acquired periventricular cysts of newborn |
| P913 | Neonatal cerebral irritability |
| P914 | Neonatal cerebral depression |
| P915 | Neonatal coma |
| P91819 | Neonatal encephalopathy, unspecified |
| P91821 | Neonatal cerebral infarction, right side of brain |
| P91822 | Neonatal cerebral infarction, left side of brain |
| P91823 | Neonatal cerebral infarction, bilateral |
| P91829 | Neonatal cerebral infarction, unspecified side |
| P9188 | Other specified disturbances of cerebral status of newborn |
| P919 | Disturbance of cerebral status of newborn, unspecified |
| |
| PDX Collection 1470 |
| P84 | Other problems with newborn |
| P9160 | Hypoxic ischemic encephalopathy [HIE], unspecified |
| P9161 | Mild hypoxic ischemic encephalopathy [HIE] |
| P9162 | Moderate hypoxic ischemic encephalopathy [HIE] |
| P9163 | Severe hypoxic ischemic encephalopathy [HIE] |
| |
| PDX Collection 1471 |
| P91821 | Neonatal cerebral infarction, right side of brain |
| P91822 | Neonatal cerebral infarction, left side of brain |
| P91823 | Neonatal cerebral infarction, bilateral |
| P91829 | Neonatal cerebral infarction, unspecified side |
| |
| PDX Collection 1472 |
| P9201 | Bilious vomiting of newborn |
| P9209 | Other vomiting of newborn |
| |
| PDX Collection 1473 |
| P930 | Grey baby syndrome |
| P938 | Other reactions and intoxications due to drugs administered to newborn |
| P961 | Neonatal withdrawal symptoms from maternal use of drugs of addiction |
| P962 | Withdrawal symptoms from therapeutic use of drugs in newborn |
| |
| PDX Collection 1474 |
| Q000 | Anencephaly |
| Q001 | Craniorachischisis |
| Q002 | Iniencephaly |
| |
| PDX Collection 1475 |
| Q010 | Frontal encephalocele |
| Q011 | Nasofrontal encephalocele |
| Q012 | Occipital encephalocele |
| Q018 | Encephalocele of other sites |
| Q019 | Encephalocele, unspecified |
| Q02 | Microcephaly |
| Q040 | Congenital malformations of corpus callosum |
| Q041 | Arhinencephaly |
| Q042 | Holoprosencephaly |
| Q043 | Other reduction deformities of brain |
| Q044 | Septo-optic dysplasia of brain |
| Q045 | Megalencephaly |
| Q046 | Congenital cerebral cysts |
| Q048 | Other specified congenital malformations of brain |
| |
| PDX Collection 1476 |
| Q044 | Septo-optic dysplasia of brain |
| Q045 | Megalencephaly |
| Q046 | Congenital cerebral cysts |
| Q048 | Other specified congenital malformations of brain |
| |
| PDX Collection 1477 |
| 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 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 |
| Q8786 | Kleefstra syndrome |
| Q8787 | Hao-Fountain Syndrome |
| Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
| Q897 | Multiple congenital malformations, not elsewhere classified |
| Q8981 | Kabuki syndrome |
| Q8989 | Other specified congenital malformations |
| Q992 | Fragile X chromosome |
| Q99811 | Usher syndrome, type 1 |
| Q99812 | Usher syndrome, type 2 |
| Q99813 | Usher syndrome, type 3 |
| Q99818 | Other Usher syndrome |
| Q99819 | Usher syndrome, unspecified |
| QA00101 | SCN2A-related neurodevelopmental disorder |
| QA00102 | CACNA1A-related neurodevelopmental disorder |
| QA00109 | Neurodevelopmental disorder related to pathogenic variant in other ion channel gene |
| QA0011 | Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes |
| QA0012 | Neurodevelopmental disorders, related to pathogenic variants in other receptor genes |
| QA00131 | SLC6A1-related disorder |
| QA00139 | Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene |
| QA00141 | Syntaxin-binding protein 1-related disorder |
| QA00142 | DLG4-related synaptopathy |
| QA00149 | Neurodevelopmental disorder, related to pathogenic variant in other synapse related gene |
| QA00151 | FOXG1 syndrome |
| QA00159 | Neurodevelopmental disorder, related to other genes associated with transcription and gene expression |
| QA08 | Other neurodevelopmental disorders related to pathogenic variants in other specific genes |
| |
| PDX Collection 1478 |
| 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 |
| 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 |
| Q2381 | Bicuspid aortic valve |
| Q2382 | Congenital mitral valve cleft leaflet |
| Q2388 | 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 |
| Q8786 | Kleefstra syndrome |
| Q8787 | Hao-Fountain Syndrome |
| Q8789 | Other specified congenital malformation syndromes, not elsewhere classified |
| Q897 | Multiple congenital malformations, not elsewhere classified |
| Q8981 | Kabuki syndrome |
| Q8989 | Other specified congenital malformations |
| Q992 | Fragile X chromosome |
| Q99811 | Usher syndrome, type 1 |
| Q99812 | Usher syndrome, type 2 |
| Q99813 | Usher syndrome, type 3 |
| Q99818 | Other Usher syndrome |
| Q99819 | Usher syndrome, unspecified |
| QA00101 | SCN2A-related neurodevelopmental disorder |
| QA00102 | CACNA1A-related neurodevelopmental disorder |
| QA00109 | Neurodevelopmental disorder related to pathogenic variant in other ion channel gene |
| QA0011 | Neurodevelopmental disorders, related to pathogenic variants in glutamate receptor genes |
| QA0012 | Neurodevelopmental disorders, related to pathogenic variants in other receptor genes |
| QA00131 | SLC6A1-related disorder |
| QA00139 | Neurodevelopmental disorder, related to pathogenic variant in other transporter or solute carrier gene |
| QA00141 | Syntaxin-binding protein 1-related disorder |
| QA00142 | DLG4-related synaptopathy |
| QA00149 | Neurodevelopmental disorder, related to pathogenic variant in other synapse related gene |
| QA00151 | FOXG1 syndrome |
| QA00159 | Neurodevelopmental disorder, related to other genes associated with transcription and gene expression |
| QA08 | Other neurodevelopmental disorders related to pathogenic variants in other specific genes |
| |
| PDX Collection 1479 |
| 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 |
| 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 |
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