Congenital/Perinatal conditions that are Major Pediatric ADGs |
|||
adgtype |
|||
icdtype |
diag |
diagnames |
|
3 = Time Limited: Major |
|||
|
9 |
74441 |
74441 |
|
9 |
747 |
747 OTH CONGENIT ANOMAL CIRCULATRY SYS |
|
9 |
7470 |
7470 PATENT DUCTUS ARTERIOSUS |
|
9 |
74720 |
74720 |
|
9 |
74721 |
74721 |
|
9 |
74722 |
74722 |
|
9 |
74729 |
74729 |
|
9 |
7473 |
7473 ANOMALIES OF PULMONARY ARTERY |
|
9 |
74740 |
74740 |
|
9 |
74741 |
74741 |
|
9 |
74742 |
74742 |
|
9 |
74749 |
74749 |
|
9 |
7480 |
7480 CHOANAL ATRESIA |
|
9 |
7482 |
7482 WEB OF LARYNX |
|
9 |
7483 |
7483 OTH ANOMAL LARYNX,TRACHEA,BRONCHUS |
|
9 |
7488 |
7488 OTH SPEC ANOMAL RESPIRATORY SYSTEM |
|
9 |
749 |
749 CLEFT PALATE AND CLEFT LIP |
|
9 |
74900 |
74900 |
|
9 |
74901 |
74901 |
|
9 |
74902 |
74902 |
|
9 |
74903 |
74903 |
|
9 |
74904 |
74904 |
|
9 |
74910 |
74910 |
|
9 |
74920 |
74920 |
|
9 |
74921 |
74921 |
|
9 |
74922 |
74922 |
|
9 |
74923 |
74923 |
|
9 |
74924 |
74924 |
|
9 |
74925 |
74925 |
|
9 |
75029 |
75029 |
|
9 |
7503 |
7503 TRACHEOESOPHAGEAL FIST,ATRES,STENO |
|
9 |
7505 |
7505 CONGENTL HYPERTRPHC PYLORC STENOS |
|
9 |
7506 |
7506 CONGENITAL HIATUS HERNIA |
|
9 |
751 |
751 OTH CONGENIT ANOMAL DIGESTIVE SYST |
|
9 |
7510 |
7510 MECKEL''S DIVERTICULUM |
|
9 |
7511 |
7511 ATRESIA & STENOSIS SMALL INTESTINE |
|
9 |
7512 |
7512 ATRES,STEN LRG INTEST,RECTM,ANAL C |
|
9 |
7514 |
7514 OTHER ANOMALIES INTESTINE FIXATION |
|
9 |
7518 |
7518 OTH SPEC ANOMALY DIGESTIVE SYSTEM |
|
9 |
7535 |
7535 EXSTROPHY OF URINARY BLADDER |
|
9 |
7536 |
7536 ATRESIA,STEN URETHRA, BLADDER NECK |
|
9 |
7537 |
7537 ANOMALIES OF URACHUS |
|
9 |
75679 |
75679 |
|
9 |
7581 |
7581 PATAU''S SYNDROME |
|
9 |
7582 |
7582 EDWARD''S SYNDROME |
|
9 |
7594 |
7594 CONJOINED TWINS |
|
9 |
7680 |
7680 FETAL DEATH ASPHYX/ANOXIA BEFR LAB |
|
9 |
7681 |
7681 FETAL DEATH ASPHYX/ANOXIA IN LABOR |
|
9 |
7685 |
7685 SEVERE BIRTH ASPHYXIA |
|
9 |
7686 |
7686 MILD/MODERATE BIRTH ASPHYXIA |
|
9 |
769 |
769 RESPIRATORY DISTRESS SYNDROME |
|
9 |
7701 |
770.1 *MECONIUM ASPIRATION SYNDROME |
|
9 |
7702 |
7702 FETUS/NB INTERST EMPHYSEMA,REL CDN |
|
9 |
7703 |
7703 PULMONARY HEMORRHAGE-FETUS/NEWBORN |
|
9 |
7704 |
7704 PRIMARY ATELECTASIS |
|
9 |
7705 |
7705 OTHER UNSPECIFIED ATELECTASIS |
|
9 |
7706 |
770.6 *TRANSITORY TACHYPNEA NEWBN-WET LUNG |
|
9 |
7707 |
7707 CHRONIC RESP DISEASE-PRENATAL PERD |
|
9 |
7721 |
7721 INTRAVENTRICULAR HEMORRHAGE |
|
9 |
7722 |
7722 SUBARACHNOID HEMORRHAGE |
|
9 |
7723 |
7723 UMBILICAL HEMORRHAGE AFTER BIRTH |
|
9 |
7724 |
7724 GASTROINTESTINAL HEMORRHAGE |
|
9 |
7725 |
7725 ADRENAL HEMORRHAGE |
|
9 |
773 |
773 HEMOLYTIC DIS FETUS/NB DUE ISOIMUN |
|
9 |
7730 |
7730 HEMOLYTIC DISEASE-RH ISOIMMUNIZATN |
|
9 |
7731 |
7731 HEMOLYTIC DISEASE-ABO ISOIMMUNIZTN |
|
9 |
7732 |
7732 HEMOLYTIC DISEASE-OTH ISOIMMUNIZTN |
|
9 |
7733 |
7733 HYDROPS FETALIS DUE ISOIMMUNIZATON |
|
9 |
7741 |
7741 PRNTL JAUNDCE-OTH EXCESS HEMOLYSIS |
|
9 |
7742 |
7742 NEONTL JAUNDICE-PRETERM DELIVERY |
|
9 |
77430 |
77430 |
|
9 |
77439 |
77439 |
|
9 |
7744 |
7744 PRENTL JAUNDCE-HEPTOCELLULAER DAMA |
|
9 |
775 |
775 ENDOCRINE/METABOLC DIS-FETUS/NEWBN |
|
9 |
7750 |
7750 "INFANT OF DIABETIC MOTHER" SYNDRM |
|
9 |
7754 |
7754 HYPOCALCEMIA/HYPOMAGNESEMIA-NEWBRN |
|
9 |
7755 |
7755 OTH TRANS NEONTL ELECTROLYT DISTRB |
|
9 |
7756 |
7756 NEONTL HYPOGLYCEMIA |
|
9 |
7758 |
7758 OTH TRANS NEONTL ENDCRN/METABL DIS |
|
9 |
7759 |
7759 UNSP ENDOCRN/METABOL DIS-FET/NEW |
|
9 |
7760 |
7760 HEMORRHAGIC DISEASE OF NEWBORN |
|
9 |
7765 |
7765 CONGENITAL ANEMIA |
|
9 |
7766 |
7766 ANEMIA OF PREMATURITY |
|
9 |
7767 |
7767 TRANSIENT NEONTL NEUTROPENIA |
|
9 |
7768 |
7768 OTH TRANS HEMATOLOGICAL DIS |
|
9 |
777 |
777 PERINATAL DISORDERS DIGESTIVE SYST |
|
9 |
7771 |
777.1 *MECONIUM OBSTRUCT/MECONIUM ILEUS NOS |
|
9 |
7776 |
7776 PERINATAL INTESTINAL PERFORATION |
|
9 |
7781 |
7781 SCLEREMA NEONATORUM |
|
9 |
7795 |
7795 DRUG WITHDRAWL SYNDROMEIN NEWBORN |
|
9 |
7796 |
7796 TERMINATION OF PREGNANCY (FETUS) |
|
10 |
Q256 |
Q25.6 : Stenosis of pulmonary artery |
|
10 |
Q257 |
Q25.7 : Other congenital malformations of pulmonary artery |
|
10 |
Q265 |
Q26.5 : Anomalous portal venous connection |
|
10 |
Q268 |
Q26.8 : Other congenital malformations of great veins |
|
10 |
Q300 |
Q30.0 : Choanal atresia |
|
10 |
Q394 |
Q39.4 : Oesophageal web |
|
10 |
Q423 |
Q42.3 : Congenital absence, atresia
and stenosis of anus without |
|
10 |
Q430 |
'Q43.0 : Meckel's diverticulum' |
|
10 |
Q433 |
Q43.3 : Congenital malformations of intestinal fixation |
|
10 |
Q912 |
Q91.2 : Trisomy 18, translocation |
11 = Chronic Medical: Unstable |
|||
9 |
7402 |
7402 INIENCEPHALY |
|
|
9 |
741 |
741 SPINA BIFIDA |
|
9 |
74100 |
74100 |
|
9 |
74101 |
74101 |
|
9 |
74102 |
74102 |
|
9 |
74103 |
74103 |
|
9 |
74190 |
74190 |
|
9 |
74191 |
74191 |
|
9 |
74192 |
74192 |
|
9 |
74193 |
74193 |
|
9 |
7423 |
7423 CONGENITAL HYDROCEPHALUS |
|
9 |
745 |
745 BULB CORDIS ANON & CARDIAC SEPT CL |
|
9 |
7450 |
7450 COMMON TRUNCUS |
|
9 |
74510 |
74510 |
|
9 |
74511 |
74511 |
|
9 |
74512 |
74512 |
|
9 |
74519 |
74519 |
|
9 |
7452 |
7452 TETRALOGY OF FALLOT |
9 |
7453 |
7453 COMMON VENTRICLE |
|
|
9 |
7455 |
7455 OSTIUM SECUND TYP ATRIL SEP DEFECT |
|
9 |
74560 |
74560 |
|
9 |
74561 |
74561 |
|
9 |
74569 |
74569 |
|
9 |
7458 |
7458 OTHER - SEPTAL CLOSURE |
|
9 |
7459 |
7459 UNSPEC DEFECT OF SEPTAL CLOSURE |
|
9 |
746 |
746 OTH CONGENITAL ANOMALIES OF HEART |
|
9 |
74600 |
74600 |
|
9 |
74601 |
74601 |
|
9 |
74602 |
74602 |
|
9 |
74609 |
74609 |
|
9 |
7461 |
7461 TRICUSPD ATRESIA,STENOSIS-CONGENIT |
|
9 |
7462 |
7462 EBSTEIN''S ANOMALY |
|
9 |
7463 |
7463 CONGENITAL STENOSIS AORTIC VALVE |
|
9 |
7464 |
7464 CONGENITAL INSUFFIC AORTIC VALVE |
|
9 |
7465 |
7465 CONGENITAL MITRAL STENOSIS |
|
9 |
7466 |
7466 CONGENITAL MITRAL INSUFFICIENCY |
|
9 |
7467 |
7467 HYPOPLASTIC LEFT HEART SYNDROME |
|
9 |
74681 |
74681 |
|
9 |
74682 |
74682 |
|
9 |
74683 |
74683 |
|
9 |
74684 |
74684 |
|
9 |
74685 |
74685 |
|
9 |
74686 |
74686 |
|
9 |
74687 |
74687 |
|
9 |
74689 |
74689 |
|
9 |
7469 |
7469 UNSPECIFIED ANOMALY OF HEART |
|
9 |
74710 |
74710 |
|
9 |
74711 |
74711 |
|
9 |
7484 |
7484 CONGENITAL CYSTIC LUNG |
|
9 |
7485 |
7485 AGENESIS,HYPOPLASIA,DYSPLASIA LUNG |
|
9 |
74860 |
74860 |
|
9 |
74861 |
74861 |
|
9 |
75160 |
75160 |
|
9 |
75161 |
75161 |
|
9 |
75162 |
75162 |
|
9 |
7530 |
7530 RENAL AGENESIS AND DYSGENESIS |
|
9 |
7531 |
7531 CYSTIC KIDNEY DISEASE |
|
9 |
75312 |
75312 |
|
9 |
75313 |
75313 |
9 |
75314 |
75314 |
|
|
9 |
75315 |
75315 |
|
9 |
75316 |
75316 |
|
9 |
7532 |
7532 OBSTRUCT DEFECT RENAL PELVS,URETER |
|
9 |
75321 |
75321 |
|
9 |
75329 |
75329 |
|
9 |
75651 |
75651 |
|
9 |
75652 |
75652 |
|
9 |
75656 |
75656 |
|
9 |
75659 |
75659 |
|
9 |
7567 |
7567 ANOMALIES OF ABDOMINAL WALL |
|
9 |
75683 |
75683 |
|
9 |
7583 |
7583 AUTOSOMAL DELETION SYNDROMES |
|
9 |
7595 |
7595 TUBEROUS SCLEROSIS |
|
9 |
7740 |
7740 PRNTL JAUNDICE-HER HEMO ANEMIAS |
|
9 |
7751 |
7751 NEONATAL DIABETES MELLITUS |
|
9 |
7752 |
7752 NEONATAL MYASTHENIA GRAVIS |
|
9 |
7753 |
7753 NEONATAL THYROTOXICOSIS |
|
10 |
Q054 |
Q05.4 : Unspecified spina bifida with
hydrocephalus |
|
10 |
Q057 |
Q05.7 : Lumbar spina bifida without
hydrocephalus |
|
10 |
Q059 |
Q05.9 : Spina bifida, unspecified |
|
10 |
Q070 |
Q07.0 : Arnold-Chiari syndrome |
|
10 |
Q213 |
Q21.3 : Tetralogy of Fallot |
|
10 |
Q222 |
Q22.2 : Congenital pulmonary valve insufficiency |
|
10 |
Q223 |
Q22.3 : Other congenital malformations of pulmonary valve |
|
10 |
Q231 |
Q23.1 : Congenital insufficiency of aortic valve |
|
10 |
Q233 |
Q23.3 : Congenital mitral insufficiency |
|
10 |
Q251 |
Q25.1 : Coarctation of aorta |
|
10 |
Q254 |
Q25.4 : Other congenital malformations of aorta |
|
10 |
Q336 |
Q33.6 : Hypoplasia and dysplasia of
lung |
|
10 |
Q444 |
Q44.4 : Choledochal cyst |
|
10 |
Q600 |
Q60.0 : Renal agenesis, unilateral |
|
10 |
Q605 |
Q60.5 : Renal hypoplasia, unspecified |
|
10 |
Q621 |
Q62.1 : Atresia and stenosis of ureter |
|
10 |
Q623 |
Q62.3 : Other obstructive defects of renal pelvis and ureter |
|
10 |
Q780 |
Q78.0 : Osteogenesis imperfecta |
|
10 |
Q782 |
Q78.2 : Osteopetrosis |
|
10 |
Q793 |
Q79.3 : Gastroschisis |
|
10 |
Q850 |
Q85.0 : Neurofibromatosis (nonmalignant) |
|
10 |
Q874 |
'Q87.4 : Marfan's syndrome' |
12= Chronic Specialty Stable-Ortho |
|||
|
9 |
75430 |
75430 |
9 |
75431 |
75431 |
|
|
9 |
75432 |
75432 |
|
9 |
75433 |
75433 |
|
9 |
75435 |
75435 |
|
9 |
75613 |
75613 |
|
9 |
75614 |
75614 |
|
9 |
75615 |
75615 |
|
9 |
75616 |
75616 |
|
9 |
75617 |
75617 |
|
9 |
7564 |
7564 CHONDRODYSTROPHY |
|
9 |
75689 |
75689 |
|
9 |
7569 |
7569 OTH UNSP ANOM MUSCULOSKELETAL SYST |
|
10 |
Q658 |
Q65.8 : Other congenital deformities of hip |
|
10 |
Q762 |
Q76.2 : Congenital spondylolisthesis |
|
10 |
Q773 |
Q77.3 : Chondrodysplasia punctata |
|
10 |
Q786 |
Q78.6 : Multiple congenital exostoses |
|
10 |
Q788 |
Q78.8 : Other specified osteochondrodysplasias |
|
10 |
Q796 |
Q79.6 : Ehlers-Danlos syndrome |
|
10 |
Q872 |
Q87.2 : Congenital malformation syndromes predominantly
involving |
13 = Chronic Specialty: Stable-ENT |
|||
10 |
Q359 |
Q35.9 : Cleft palate, unspecified |
|
18 = Chronic Specialty: Unstable-Eye |
|||
9 |
74320 |
74320 |
|
|
9 |
74322 |
74322 |
|
10 |
Q150 |
Q15.0 : Congenital glaucoma |
$Id:
/project/child_ses/prog/phongsackm/mb7889_2008/Diags/Unique/ICD_codes2.sas
February 19, 2009 phongsackm $ |