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Birth defect
This is important for 173./183./193./203. Congenital Anomalies in the birth outcome tab.

Options and codes

None	NONE
Abdominal Wall	ABDOM
Abdominal Wall\|Bladder exstrophy	A0015
Abdominal Wall\|Body stalk anomaly (limb body wall complex)	A0020
Abdominal Wall\|Cloacal extrophy	A0030
Abdominal Wall\|Gastroschisis	A0040
Abdominal Wall\|Limb body wall complex (body stalk anomaly)	A0050
Abdominal Wall\|Omphalocele (exomphalos)	A0060
Abdominal Wall\|Other - congenital malformations of abdominal wall	A0090
Abdominal Wall\|Pentalogy of Cantrell	A0070
Abdominal Wall\|Umbilical hernia	A0080
Cardiovascular	CARDIO
Cardiovascular\|Aorta - pulmonary window	A0110
Cardiovascular\|Aortic arch - double	A0120
Cardiovascular\|Aortic arch - interrupted	A0130
Cardiovascular\|Aortic atresia	A0140
Cardiovascular\|Aortic valve insufficiency	A0150
Cardiovascular\|Aortic valve stenosis	A0160
Cardiovascular\|Arrhythmia	A0170
Cardiovascular\|Atrial fibrillation	A0180
Cardiovascular\|Atrial flutter	A0190
Cardiovascular\|Atrial septal defect (ASD)	A0200
Cardiovascular\|Atrioventricular septal defect (AVSD) (endocardial cushion defect)	A0210
Cardiovascular\|Bilateral SVC (superior vena cava)	A0220
Cardiovascular\|Bradycardia (bradyarrhythmia)	A0230
Cardiovascular\|Cardiac dysfunction	A0240
Cardiovascular\|Cardiac tumour / mass	A0250
Cardiovascular\|Cardiomegaly	A0260
Cardiovascular\|Cardiomyopathy - dilated	A0270
Cardiovascular\|Cardiomyopathy - fetus of diabetic mother	A0280
Cardiovascular\|Cardiomyopathy - hypertrophic (HOCM)	A0290
Cardiovascular\|Coarctation of aorta	A0300
Cardiovascular\|Common atrium	A0310
Cardiovascular\|Complete Heart Block	A0320
Cardiovascular\|Congenital heart block (CHB)	A0330
Cardiovascular\|Congenital heart disease	A0340
Cardiovascular\|Coronary artery fistula	A0350
Cardiovascular\|Dextrocardia	A0360
Cardiovascular\|Dilated ascending aorta	A0370
Cardiovascular\|Diverticulum - LV	A0380
Cardiovascular\|Diverticulum - RV	A0390
Cardiovascular\|Double inlet left ventricle (DILV)	A0400
Cardiovascular\|Double inlet right ventricle (DIRV)	A0410
Cardiovascular\|Double outlet left ventricle (DOLV)	A0420
Cardiovascular\|Double outlet right ventricle (DORV)	A0430
Cardiovascular\|Ductus arteriosus - Patent (PDA)	A6001
Cardiovascular\|Ductus arteriosus - premature closure	A0440
Cardiovascular\|Ductus arteriosus aneurysm	A0450
Cardiovascular\|Ductus venosus - agenesis	A0460
Cardiovascular\|Ebstein anomaly	A0470
Cardiovascular\|Ectopia cordis	A0490
Cardiovascular\|EFE (endocardial fibroelastosis)	A0500
Cardiovascular\|Endocardial fibroelastosis (EFE)	A0510
Cardiovascular\|Fibroma - cardiac	A0520
Cardiovascular\|HLHS (hypoplastic left heart syndrome)	A0530
Cardiovascular\|Hypoplastic aortic arch	A0540
Cardiovascular\|Hypoplastic left heart syndrome (HLHS)	A0550
Cardiovascular\|Hypoplastic right heart syndrome (HRHS)	A0560
Cardiovascular\|Interrupted IVC (superior vena cava)	A0570
Cardiovascular\|Left atrial isomerism (heterotaxy)	A0580
Cardiovascular\|Mitral atresia	A6002
Cardiovascular\|Mitral regurGastrointestinalation	A0590
Cardiovascular\|Mitral stenosis	A0600
Cardiovascular\|Mitral valve dysplasia	A0610
Cardiovascular\|Other - cardiac malformations not classified elsewhere	A0990
Cardiovascular\|Other heart abnormalities	A1000
Cardiovascular\|Partial anomalous pulmonary venous drainage (PAPVD)	A0620
Cardiovascular\|Pericardial cyst	A0630
Cardiovascular\|Pericardial effusion	A0640
Cardiovascular\|Persistent left SVC (superior vena cava)	A0650
Cardiovascular\|Premature atrial contractions (PAC's)	A0660
Cardiovascular\|Premature closure of atrial septum (PFO)	A0670
Cardiovascular\|Premature ventricular contractions (PVC's)	A0680
Cardiovascular\|Pulmonary (valve) atresia	A0690
Cardiovascular\|Pulmonary (valve) stenosis (PS)	A0700
Cardiovascular\|Pulmonary insufficiency	A0710
Cardiovascular\|Pulmonary valve dysplasia	A0720
Cardiovascular\|Rhabdomyoma(s) - cardiac	A0730
Cardiovascular\|Right arch	A0740
Cardiovascular\|Right atrial isomerism (heterotaxy)	A0750
Cardiovascular\|Scimitar syndrome	A0760
Cardiovascular\|Shone's syndrome	A0770
Cardiovascular\|Single outlet ventricle	A0780
Cardiovascular\|Single ventricle (univentricular heart)	A0790
Cardiovascular\|Single ventricle / univentricular connection	A0800
Cardiovascular\|Situs inversus - cardiac	A0810
Cardiovascular\|Subaortic stenosis	A0820
Cardiovascular\|Supra ventricular tachycardia (SVT)	A0830
Cardiovascular\|Tachycardia (tachyarrhythmia)	A0840
Cardiovascular\|TAPVD (total anomalous pulmonary venous drainage)	A0850
Cardiovascular\|Tetralogy of Fallot (TOF)	A0860
Cardiovascular\|Total anomalous pulmonary venous drainage (TAPVD)	A0870
Cardiovascular\|Transposition of great arteries - complete (CTGA)	A0880
Cardiovascular\|Transposition of great arteries - congenitally corrected (CCTGA)	A0890
Cardiovascular\|Transposition of great vessels (TGA)	A0900
Cardiovascular\|Tricuspid atresia	A0910
Cardiovascular\|Tricuspid regurGastrointestinalation	A0920
Cardiovascular\|Tricuspid stenosis	A0930
Cardiovascular\|Tricuspid valve dysplasia	A0940
Cardiovascular\|Truncus arteriosis	A0950
Cardiovascular\|Valvular Anomalies	A0961
Cardiovascular\|Vascular ring	A0960
Cardiovascular\|Ventricular disproportion (RV>LV)	A6003
Cardiovascular\|Ventricular septal defect (VSD)	A0970
Cardiovascular\|Ventricular tachycardia	A0980
Chromosomes	CHROM
Chromosomes\|45,X (Turner syndrome)	A1020
Chromosomes\|47,XXX	A1030
Chromosomes\|47,XXY (Klinefelter syndrome)	A1040
Chromosomes\|47,XYY	A1050
Chromosomes\|Array CGH abnormal or other	A1060
Chromosomes\|Balanced translocation	A1070
Chromosomes\|Deletion - other	A1080
Chromosomes\|Di George Syndrome (22 q11 deletion)	A1090
Chromosomes\|Microdeletion syndrome - other	A1100
Chromosomes\|Mosaicism	A1110
Chromosomes\|Normal female; 46,XX	A1120
Chromosomes\|Normal male; 46,XY	A1130
Chromosomes\|Other	A1240
Chromosomes\|Paracentric inversion	A1140
Chromosomes\|Pericentric inversion	A1150
Chromosomes\|Triploidy /polploidy	A1160
Chromosomes\|Trisomy - other	A1170
Chromosomes\|Trisomy 13	A1180
Chromosomes\|Trisomy 18	A1190
Chromosomes\|Trisomy 21 (Down syndrome)	A1200
Chromosomes\|Trisomy 21 (Down syndrome) - mosaic	A1210
Chromosomes\|Trisomy 21 (Down syndrome) - translocation	A1220
Chromosomes\|Unbalanced translocation	A1230
Congenital Infections	CONGINF
Congenital Infections\|CMV (cytomegalovirus) infection - congenital	A1260
Congenital Infections\|Enterovirus infections	A1270
Congenital Infections\|Herpes simplex virus (HSV) infection - congenital	A1280
Congenital Infections\|HIV	A1290
Congenital Infections\|Other - infections	A1340
Congenital Infections\|Rubella syndrome - congenital	A1300
Congenital Infections\|Toxoplasmosis	A1310
Congenital Infections\|Tuberculosis (TB) - congenital	A1320
Congenital Infections\|Varicella-zoster virus	A1330
Extremities-skeletal	EXTSKE
Extremities-skeletal\|Abnormalities	A1351
Extremities-skeletal\|Arms/legs	A1360
Extremities-skeletal\|Arms/legs-Bowed femur	A1370
Extremities-skeletal\|Arms/legs-Bowed humerus	A1380
Extremities-skeletal\|Arms/legs-Bowed radius &/or ulna	A1390
Extremities-skeletal\|Arms/legs-Bowed tibia &/or fibula	A1400
Extremities-skeletal\|Arms/legs-Fracture(s) - long bones	A1410
Extremities-skeletal\|Generalized/other	A1420
Extremities-skeletal\|Generalized/other-Akinesia deformation sequence; fetal (FADS)	A1430
Extremities-skeletal\|Generalized/other-Arthrogryposis multiplex congenita	A1440
Extremities-skeletal\|Generalized/other-Congenital malformations of spine & bony thorax	A1450
Extremities-skeletal\|Generalized/other-Fixed flexion deformity	A1460
Extremities-skeletal\|Generalized/other-Fracture(s) - ribs	A1470
Extremities-skeletal\|Generalized/other-Hip Dislocation; congenital	A1480
Extremities-skeletal\|Generalized/other-Hypomineralization	A1490
Extremities-skeletal\|Generalized/other-Limb reduction defect(s) (LRD) - lower limb	A1500
Extremities-skeletal\|Generalized/other-Limb reduction defect(s) (LRD) - upper limb	A1510
Extremities-skeletal\|Generalized/other-Malformation of sternum	A1520
Extremities-skeletal\|Generalized/other-Phocomelia	A1530
Extremities-skeletal\|Generalized/other-Sirenomelia	A1540
Extremities-skeletal\|Generalized/other-Skeletal dysplasia -other	A1550
Extremities-skeletal\|Hands/feet	A1560
Extremities-skeletal\|Hands/feet-Adactyly (absent fingers/ toes)	A1570
Extremities-skeletal\|Hands/feet-Brachydactyly (short fingers/toes)	A1580
Extremities-skeletal\|Hands/feet-Clenched hands (persistently)	A1590
Extremities-skeletal\|Hands/feet-Clinodactyly (fifth finger)	A1600
Extremities-skeletal\|Hands/feet-Club foot	A1610
Extremities-skeletal\|Hands/feet-Ectrodactyly (lobster-claw / cleft hand)	A1620
Extremities-skeletal\|Hands/feet-Fused toes	A1630
Extremities-skeletal\|Hands/feet-Overlapping fingers	A1640
Extremities-skeletal\|Hands/feet-Polydactyly (feet)	A1650
Extremities-skeletal\|Hands/feet-Polydactyly (hands)	A1660
Extremities-skeletal\|Hands/feet-Radial ray anomaly (absent thumb)	A1670
Extremities-skeletal\|Hands/feet-Rocker-bottom feet	A1680
Extremities-skeletal\|Hands/feet-Sandal gap toes	A1690
Extremities-skeletal\|Hands/feet-Syndactyly (feet)	A1700
Extremities-skeletal\|Hands/feet-Syndactyly (hands)	A1710
Extremities-skeletal\|Hands/feet-Webbed fingers	A1720
Extremities-skeletal\|Hands/feet-Webbed toes	A1730
Extremities-skeletal\|Micromelia	A6004
Extremities-skeletal\|Muscle/connective tissue disorders	A1740
Extremities-skeletal\|Muscle/connective tissue disorders-Duchenne muscular dystrophy (DMD)	A1750
Extremities-skeletal\|Muscle/connective tissue disorders-Ehlers-Danlos syndrome	A1760
Extremities-skeletal\|Muscle/connective tissue disorders-Hypotonia	A1770
Extremities-skeletal\|Muscle/connective tissue disorders-Other - malformations of the musculoskeletal system	A1790
Extremities-skeletal\|Muscle/connective tissue disorders-Spinal muscular atrophy (SMA)	A1780
Extremities-skeletal\|Skeletal Dysplasias	A1800
Extremities-skeletal\|Skeletal Dysplasias-Achondrogenesis	A1810
Extremities-skeletal\|Skeletal Dysplasias-Achondroplasia	A1820
Extremities-skeletal\|Skeletal Dysplasias-Campomelic dysplasia	A1830
Extremities-skeletal\|Skeletal Dysplasias-Chondrodysplasia punctata	A1840
Extremities-skeletal\|Skeletal Dysplasias-Diastrophic dysplasia	A1850
Extremities-skeletal\|Skeletal Dysplasias-Ellis-van Creveld syndrome	A1860
Extremities-skeletal\|Skeletal Dysplasias-Osteogenesis imperfecta	A1870
Extremities-skeletal\|Skeletal Dysplasias-Short rib polydactyly syndrome - type VII	A1880
Extremities-skeletal\|Skeletal Dysplasias-Thanatophoric dysplasia	A1890
Extremities-skeletal\|Syndactyly	A6005
Face	FACE
Face\|Abnormalities	A2031
Face\|EARS	A1910
Face\|EARS-Ears - absent (anotia)	A1920
Face\|EARS-Ears - low set	A1930
Face\|EARS-Ears - small (microtia)	A1940
Face\|EYES	A1950
Face\|EYES-Anophthalmia	A1960
Face\|EYES-Congenital cataract	A1970
Face\|EYES-Cyclops	A1980
Face\|EYES-Hypertelorism	A1990
Face\|EYES-Hypotelorism	A2000
Face\|EYES-Macrophthalmia	A2010
Face\|EYES-Microphthalmia	A2020
Face\|EYES-Retinoblastoma	A2030
Face\|MOUTH	A2040
Face\|MOUTH-Cleft lip	A2050
Face\|MOUTH-Cleft lip & palate	A2060
Face\|MOUTH-Cleft palate	A2070
Face\|MOUTH-Flat face	A2080
Face\|MOUTH-Macroglossia	A2090
Face\|MOUTH-Micrognathia	A2100
Face\|MOUTH-Retrognathia	A2110
Face\|NOSE	A2120
Face\|NOSE-Absent nose	A2140
Face\|NOSE-Choanal atresia	A2160
Face\|NOSE-Hypoplastic nose	A2180
Face\|NOSE-Proboscis	A2190
Face\|NOSE-Single nostril	A2200
Face\|Other - malformations of the face	A2230
Face\|Tumour of face	A2210
Face\|Tumour of face Other	A2220
Gastrointestinal	GASTRO
Gastrointestinal\|Bowel obstruction small or large intestine	A2665
Gastrointestinal\|Stenois small or large intestine	A2915
Gastrointestinal\|Abnormal Esophagus	A2591
Gastrointestinal\|Abnormal Gallbladder	A2592
Gastrointestinal\|Abnormal Large Bowel	A2593
Gastrointestinal\|Abnormal Liver	A2594
Gastrointestinal\|Abnormal Small Bowel	A2595
Gastrointestinal\|Abnormal Stomach	A2596
Gastrointestinal\|Absent gallbladder	A2600
Gastrointestinal\|Absent stomach	A2610
Gastrointestinal\|Adrenal cyst(s)	A2620
Gastrointestinal\|Ascites	A2630
Gastrointestinal\|Asplenia	A2640
Gastrointestinal\|Atresia and stenosis intestine	A2650
Gastrointestinal\|Biliary atresia	A2660
Gastrointestinal\|Choledochal cyst(s)	A2670
Gastrointestinal\|Dilated gallbladder	A2680
Gastrointestinal\|Dilated stomach	A2690
Gastrointestinal\|Duodenal atresia	A2700
Gastrointestinal\|Hepatomegaly	A2710
Gastrointestinal\|Hirschsprung's disease	A2720
Gastrointestinal\|Hyperperistalsis	A2730
Gastrointestinal\|Imperforate anus	A2740
Gastrointestinal\|Intra-abdominal cyst(s)	A2750
Gastrointestinal\|Large bowel obstruction	A2760
Gastrointestinal\|Liver cyst(s)	A2770
Gastrointestinal\|Liver nodule	A2780
Gastrointestinal\|Meconium ileus	A2790
Gastrointestinal\|Meconium peritonitis	A2800
Gastrointestinal\|Mesenteric cyst	A2810
Gastrointestinal\|Oesophageal atresia	A2820
Gastrointestinal\|Oesophageal diverticulum	A2830
Gastrointestinal\|Other - malformations of the gastro-intestinal tract	A2930
Gastrointestinal\|Ovarian cyst(s)	A2840
Gastrointestinal\|Pancreatic cyst(s)	A2850
Gastrointestinal\|Perinatal intestinal perforation	A2860
Gastrointestinal\|Polysplenia	A2870
Gastrointestinal\|Pyloric stenosis	A2880
Gastrointestinal\|Situs inversus - abdominal	A2890
Gastrointestinal\|Small bowel obstruction	A2900
Gastrointestinal\|Small stomach	A6009
Gastrointestinal\|Splenomegaly	A2910
Gastrointestinal\|Tracheo-oesophageal fistula (TEF)	A2920
Genitourinary Tract	GENTRCT
Genitourinary Tract\|Absent bladder	A6006
Genitourinary Tract\|Ambiguous genitalia / indeterminate sex	A2250
Genitourinary Tract\|Autosomal dominant polycystic kidney disease (ADPKD)	A2260
Genitourinary Tract\|Autosomal recessive polycystic kidney disease (ARPKD)	A2270
Genitourinary Tract\|Bladder abnormalities	A2271
Genitourinary Tract\|Bladder diverticulum	A2280
Genitourinary Tract\|Bladder extrophy	A2290
Genitourinary Tract\|Cloacal dysgenesis	A2300
Genitourinary Tract\|Cloacal extrophy	A2310
Genitourinary Tract\|Cystic kidney(s) - other	A2320
Genitourinary Tract\|Duplex kidney/collecting system	A2330
Genitourinary Tract\|Echogenic kidney(s)	A2340
Genitourinary Tract\|Ectopic/pelvic kidney	A2350
Genitourinary Tract\|Hydrocoele	A2360
Genitourinary Tract\|Hydronephrosis (>10 mm)	A2370
Genitourinary Tract\|Hyperplastic & giant kidney(s)	A2380
Genitourinary Tract\|Hypoplastic kidney(s)	A2390
Genitourinary Tract\|Hypospadias	A2400
Genitourinary Tract\|Keyhole bladder/urethra	A6007
Genitourinary Tract\|Keyhole sign	A6008
Genitourinary Tract\|Lower urinary tract obstruction (LUTO)	A2410
Genitourinary Tract\|Megacystis	A2420
Genitourinary Tract\|Megaureter	A2430
Genitourinary Tract\|Multicystic kidney disease (MCKD)	A2440
Genitourinary Tract\|Other - malformations of female genitalia	A2560
Genitourinary Tract\|Other - malformations of male genitalia	A2570
Genitourinary Tract\|Other - malformations of urinary system	A2580
Genitourinary Tract\|Posterior urethral valves (PUV)	A2450
Genitourinary Tract\|Prune belly	A2460
Genitourinary Tract\|Pseudohermaphroditism	A2470
Genitourinary Tract\|Renal Abnormalities	A2481
Genitourinary Tract\|Renal agenesis	A2490
Genitourinary Tract\|Renal cyst	A2500
Genitourinary Tract\|Renal dysplasia	A2510
Genitourinary Tract\|Undescended testicle(s)	A2520
Genitourinary Tract\|Ureter Abnormalities	A2521
Genitourinary Tract\|Ureterocoele	A2530
Genitourinary Tract\|Urethral atresia	A2540
Genitourinary Tract\|Urethral obstruction malformation complex	A2550
Head-Cranium & Brain	HEADCB
Head-Cranium & Brain\|Absent cerebellar vermis	A2950
Head-Cranium & Brain\|Absent cerebellum	A2960
Head-Cranium & Brain\|Acrania	A2970
Head-Cranium & Brain\|Agenesis of corpus callosum (ACC)	A2980
Head-Cranium & Brain\|Anencephaly	A2990
Head-Cranium & Brain\|Aqueductal stenosis	A3000
Head-Cranium & Brain\|Arachnoid cyst(s)	A3010
Head-Cranium & Brain\|Arhinencephaly	A3020
Head-Cranium & Brain\|Arnold Chiari malformation	A3030
Head-Cranium & Brain\|Atresia of foramina of Magendie & Luschka	A3040
Head-Cranium & Brain\|Banana cerebellum	A3050
Head-Cranium & Brain\|Brachycephaly	A3060
Head-Cranium & Brain\|Brain tumor	A3070
Head-Cranium & Brain\|Calcification - intracranial	A3080
Head-Cranium & Brain\|Cavum Septi Pellucidum (CSP) absent	A6010
Head-Cranium & Brain\|Cerebellar & posterior fossa haemorrhage	A3090
Head-Cranium & Brain\|Cerebral AVM (arteriovenous malformation)	A3100
Head-Cranium & Brain\|Cloverleaf shaped head	A3120
Head-Cranium & Brain\|Congenital cerebral cysts	A3130
Head-Cranium & Brain\|Craniorachischisis	A3140
Head-Cranium & Brain\|Craniosynostosis	A3150
Head-Cranium & Brain\|Dandy-Walker malformation / variant (DWM)	A3160
Head-Cranium & Brain\|Dolichocephaly	A3170
Head-Cranium & Brain\|Encephalocele	A3180
Head-Cranium & Brain\|Enlarged cisterna magna	A3190
Head-Cranium & Brain\|Excencephaly	A3200
Head-Cranium & Brain\|Exencephaly	A3210
Head-Cranium & Brain\|Holoprosencephaly	A3220
Head-Cranium & Brain\|Hydranencephaly	A3230
Head-Cranium & Brain\|Hydrocephalus	A3240
Head-Cranium & Brain\|Iniencephaly	A3250
Head-Cranium & Brain\|Intracerebral haemorrhage	A3260
Head-Cranium & Brain\|Intraventricular haemorrhage (IVH)	A3270
Head-Cranium & Brain\|Lissenchephaly	A3280
Head-Cranium & Brain\|Macrocephaly	A3290
Head-Cranium & Brain\|Megalencephaly	A3300
Head-Cranium & Brain\|Microcephaly	A3310
Head-Cranium & Brain\|Other - malformations of the head & Brain	A3440
Head-Cranium & Brain\|Plagiocephaly	A3320
Head-Cranium & Brain\|Porencephalic cyst(s)	A3330
Head-Cranium & Brain\|Posterior fossa cyst	A3340
Head-Cranium & Brain\|Prominent forehead	A3350
Head-Cranium & Brain\|Prominent occiput	A3360
Head-Cranium & Brain\|Seizures	A3370
Head-Cranium & Brain\|Septo-optic dysplasia	A3380
Head-Cranium & Brain\|Small cerebellum	A3390
Head-Cranium & Brain\|Subarachnoid haemorrhage	A3400
Head-Cranium & Brain\|Vein of Galen aneurysm	A3410
Head-Cranium & Brain\|Ventriculomegaly - mild (10-15 mm)	A3420
Head-Cranium & Brain\|Ventriculomegaly - severe (>15 mm)	A3430
Neck	NECK
Neck\|Cervical teratoma	A3460
Neck\|Cystic hygroma	A3470
Neck\|Neck tumour - other	A3490
Neck\|Other - malformations of the neck	A3500
Spine - Back	SPINE
Spine - Back\|Ankylosing spondylitis	A3520
Spine - Back\|Caudal regression syndrome	A3530
Spine - Back\|NTD (neural tube defect) with hydrocephalus	A3540
Spine - Back\|NTD (neural tube defect) without hydrocephalus	A3550
Spine - Back\|Other - malformations of the spine	A3580
Spine - Back\|Sacral agenesis	A3560
Spine - Back\|Sacrococcygeal teratoma (SCT)	A3570
Structural-other	STRCTO
Structural-other\|Hydrops Fetalis	A3615
Structural-other\|Amniotic Bands	A3600
Structural-other\|Failure to thrive	A3610
Structural-other\|Normal - no anomaly detected	A3620
Structural-other\|Other - malformations not classified elsewhere	A3630
Syndromes	SYNDR
Syndromes\|Aarskogs Syndrome	A3650
Syndromes\|Achondrogenesis	A3660
Syndromes\|Achondroplasia	A3670
Syndromes\|Acroesomelic Dysplasia	A3680
Syndromes\|Acrofacial Dysostosis	A3690
Syndromes\|Adrenal Hyperplasia	A3700
Syndromes\|Alpha-1-Antitrypsin	A3710
Syndromes\|Alports Syndrome	A3720
Syndromes\|Amyloplasia Congenita	A3730
Syndromes\|Angelmans Syndrome	A3740
Syndromes\|Anophthalmia	A3750
Syndromes\|Aqueductal stenosis - X linked (L1 syndrome)	A3760
Syndromes\|Arthrogryposis Multiplex Congenitia	A3770
Syndromes\|Ataxia-telangiectasis	A3780
Syndromes\|Autosomal dominant polycystic kidney disease	A3790
Syndromes\|Autosomal Recessive Polycystic Kidney Disease	A3800
Syndromes\|Beckwith-Wiedemann	A3810
Syndromes\|Biotinidase deficiency (BIOT)	A3820
Syndromes\|CADASIL	A3830
Syndromes\|CAH (Congenital Adrenal Hyperplasia)	A3840
Syndromes\|Camptomelic dysplaia	A3850
Syndromes\|Carnitine uptake defect (CUD)	A3860
Syndromes\|Caudal regression syndrome	A3870
Syndromes\|Cerebral Palsy	A3880
Syndromes\|Charcot-Marie-Tooth	A3890
Syndromes\|CHARGE association	A3900
Syndromes\|Chronrodysplasia Punctata	A3910
Syndromes\|Cleidocranial Dysplasia	A3920
Syndromes\|Coffin-Lowry syndrome	A3930
Syndromes\|Congenital hypothyroidism (HYPOTH)	A3940
Syndromes\|Congenital Myotonic Dystrophy	A3950
Syndromes\|Congenital Nephrotic Syndrome	A3960
Syndromes\|Cornelia Delange	A3970
Syndromes\|CPS (Carbamyl Phosphate Deficiency)	A3980
Syndromes\|Craniosynotsis Saethre-Crouzon	A3990
Syndromes\|Cri-du-Chat Syndrome	A4000
Syndromes\|Crouzon's syndrome	A4010
Syndromes\|Cryptophthalmus	A4020
Syndromes\|Cystic Fibrosis	A4030
Syndromes\|Dandy-walker syndrome	A4040
Syndromes\|Dextrocardia	A4050
Syndromes\|Diastrophic dysplasia	A4060
Syndromes\|Digeorge Syndrome	A4070
Syndromes\|Dysautonomia - familial	A4080
Syndromes\|Ectodermal Dysplasia	A4090
Syndromes\|Ehlers-Danlos syndrome	A4100
Syndromes\|Ellis Van Creveld Syndrome	A4110
Syndromes\|Epidermolysis Bullosa	A4120
Syndromes\|Fabry's Disease	A4140
Syndromes\|Factor V	A4150
Syndromes\|Fanconi Anemia	A4160
Syndromes\|F-HYPDRR Familial hypophosphatemia	A4130
Syndromes\|Fragile X Syndrome	A4170
Syndromes\|Fraser Syndrome - cryptophthalmos syndrome	A4180
Syndromes\|Freeman-Sheldon Syndrome	A4190
Syndromes\|Friederichs Ataxia	A4200
Syndromes\|Frontonasal dysplasia	A4210
Syndromes\|FSHD (Fascioscapulohumeral Muscular Dystrophy)	A4220
Syndromes\|Galactosemia (GALT)	A4230
Syndromes\|Gaucher	A4240
Syndromes\|Gilbert's disease	A4250
Syndromes\|Glucose-6-phosphate dehydrogenase (G6PD)	A4260
Syndromes\|Glutaric acidemia type I (GA I)	A4270
Syndromes\|Goldenhar Syndrome	A4280
Syndromes\|Gorlin Syndrome	A4290
Syndromes\|GSD (Glycogen Storage Disease)	A4300
Syndromes\|Hard +/- e syndrome	A4310
Syndromes\|Harlequin Icthyosis	A4320
Syndromes\|Hemi-hypertrophy	A4330
Syndromes\|Hemophilia A/ B	A4340
Syndromes\|Hereditary nephritis	A4350
Syndromes\|HHT (Hereditary Hemorrhagic Telangiectasia)	A4360
Syndromes\|HME (Hereditary Multiple Exostoses)	A4370
Syndromes\|Holt-Oram	A4380
Syndromes\|Homocystinosis	A4390
Syndromes\|Homocystinuria (HCY)	A4400
Syndromes\|Hunters Sundrome	A4410
Syndromes\|Hurlers Syndrome	A4420
Syndromes\|Hydrochephalus X-Linked	A4430
Syndromes\|Hydrolethalus	A4440
Syndromes\|Hypochondroplasia	A4450
Syndromes\|Hypoglycemia	A4460
Syndromes\|Hypophosphatasia	A4470
Syndromes\|Ichthyosis (non X-linked)	A4482
Syndromes\|Ichthyosis X-linked (STS deficiency)	A4484
Syndromes\|Idiopathic hypoparathyroidism	A4487
Syndromes\|Incontinentia Pigmenti	A4500
Syndromes\|Isovaleric academia (IVA)	A4510
Syndromes\|Ivemark Syndrome	A4520
Syndromes\|Jourbert Syndrome	A4530
Syndromes\|Klippel-Trenaunay Syndrome	A4540
Syndromes\|Krabbe	A4550
Syndromes\|Larsen Syndrome	A4560
Syndromes\|LCHAD	A4570
Syndromes\|Leigh's Syndrome	A4580
Syndromes\|Lesch Nyhan	A4590
Syndromes\|Limb girdle dystrophy	A4600
Syndromes\|Limb-Girdle Muscular Dystrophy	A4610
Syndromes\|Long Q-T Syndrome	A4620
Syndromes\|Lysosmal Storage Disease (IEM)	A4630
Syndromes\|Machado-Joseph Disease	A4640
Syndromes\|Maple syrup urine disease (MSUD)	A4650
Syndromes\|Marfan syndrome	A4660
Syndromes\|McKusic-Koffman Syndrome	A4670
Syndromes\|Meckel-Gruber syndrome	A4680
Syndromes\|Medium chain acyl-CoA dehydrogenase deficiency (MCAD)	A4690
Syndromes\|MELAS	A4700
Syndromes\|Menkes	A4710
Syndromes\|MERFF	A4720
Syndromes\|Metachromatic Leukodystrophy	A4730
Syndromes\|Methylenetetrahydrofolate Reductase Deficiency	A4740
Syndromes\|Methylmalonic Acidemia	A4750
Syndromes\|Methylmalonic acidemia (Cbl A;B)	A4760
Syndromes\|Methylmalonic acidemia (mutase deficiency) (MUT)	A4770
Syndromes\|Miller-Dieker Syndrome	A4780
Syndromes\|Morquio Syndrome	A4790
Syndromes\|MPS (Mucopolysaccharidosis)	A4800
Syndromes\|Multiple carboxylase deficiency (MCD)	A4810
Syndromes\|Multiple Congenital Anomalies (Unknown Origin)	A4820
Syndromes\|Multiple pterygium syndrome	A4830
Syndromes\|Myotonic Dystrophy	A4840
Syndromes\|Nail-Patella Syndrome	A4850
Syndromes\|Neurofibromatosis 1	A4860
Syndromes\|Neurofibromatosis 2	A4870
Syndromes\|Nieman-Pick	A4880
Syndromes\|Noonan Syndrome	A4890
Syndromes\|OculodentiodiGastrointestinalal Syndrome	A4900
Syndromes\|Opitz Syndrome	A4910
Syndromes\|Oromandibular Limb Hypogenesis	A4920
Syndromes\|Osteogenesis Imperfecta	A4930
Syndromes\|OTC Deficiency	A4940
Syndromes\|Otosclerosis	A4950
Syndromes\|Pallister-Hall Syndrome	A4960
Syndromes\|Pelizaeus-merzbacher-like disease	A4970
Syndromes\|Peters' anomaly (brachymesomelia)	A4980
Syndromes\|Peutz-Jeghers Syndrome	A4990
Syndromes\|Pfeiffer Syndrome	A5000
Syndromes\|Pick's Disease	A5010
Syndromes\|Pierre Robin	A5020
Syndromes\|PKU	A5030
Syndromes\|Poland Sequence Syndrome	A5040
Syndromes\|Pompe's disease	A5050
Syndromes\|Porphyria	A5060
Syndromes\|Potter's Syndrome	A5070
Syndromes\|Prader Willi	A5080
Syndromes\|Progeria	A5090
Syndromes\|Progressive Spinobulbar muscular atrophy	A5100
Syndromes\|Propionic acidemia (PROP)	A5110
Syndromes\|Protein C deficiency	A5120
Syndromes\|Proteus Syndrome	A5130
Syndromes\|Prune belly syndrome	A5140
Syndromes\|Pyruvate Carboxylase Deficiency	A5150
Syndromes\|Pyruvate Dehydrogenase Deficiency	A5160
Syndromes\|Renal Adysplasia	A5170
Syndromes\|Restrictive Dermopathy	A5180
Syndromes\|Retinis Pigmentosa	A5190
Syndromes\|Retinoblastoma	A5200
Syndromes\|Rubenstein-Taybi Syndrome	A5210
Syndromes\|Russell-Silver Syndrome	A5220
Syndromes\|Short rib polydactyly syndrome - type VII	A5230
Syndromes\|Short-rib-Polydactyly Syndrome	A5240
Syndromes\|Sialidosis	A5250
Syndromes\|Sickle Cell Anemia	A5260
Syndromes\|Situs Ambiguous	A5270
Syndromes\|Sjogren syndrome	A5280
Syndromes\|Smith-Lemli-Opitz	A5290
Syndromes\|Smith-Magenis Syndrome	A5300
Syndromes\|Sotos Syndrome	A5310
Syndromes\|Spinal Muscular Atrophy	A5320
Syndromes\|Stickler Syndrome	A5330
Syndromes\|Sturge-Weber Syndrome	A5340
Syndromes\|Syndrome not otherwise specified	A5350
Syndromes\|TAR (thrombocytopenia-absent radius) syndrome	A5360
Syndromes\|Tay-Sachs - gm2-gangliosidosis type 1	A5370
Syndromes\|Thalassaemia-alpha	A5380
Syndromes\|Thalassemia-beta	A5390
Syndromes\|Thanantrophic dysplasis	A5400
Syndromes\|Treacher Collins syndrome	A5410
Syndromes\|Tuberous Sclerosis	A5420
Syndromes\|Tumours (Sacrococcygeal Teratoma; Paragangliomata)	A5430
Syndromes\|Tyrosinemia type I (TYR I)	A5440
Syndromes\|VATER syndrome	A5450
Syndromes\|Very long-chain acyl-CoA dehydrogenase deficiency (VLCAD)	A5460
Syndromes\|Von Willibrand Disease	A5470
Syndromes\|Waardenberg Syndrome	A5480
Syndromes\|Walker-Warburg Syndrome	A5490
Syndromes\|Williams syndrome (idiopathic hypercalcaemia)	A5500
Syndromes\|Wilson Disease	A5510
Syndromes\|Wolf-hirschhorn syndrome	A5520
Syndromes\|Xeroderma Pigmentosum	A5530
Syndromes\|Zellweger (cerebro-hepato-renal) syndrome	A5540
Teratogenic Exposures	TERAEXP
Teratogenic Exposures\|Diabetic Embryopathy	A5560
Teratogenic Exposures\|Etretinate embryopathy	A5570
Teratogenic Exposures\|Fetal alcohol syndrome	A5580
Teratogenic Exposures\|Fetal aminopterin/methotrexate syndrome	A5590
Teratogenic Exposures\|Fetal hydantoin syndrome	A5600
Teratogenic Exposures\|Fetal valproate syndrome	A5610
Teratogenic Exposures\|Isotretinoin teratogen syndrome	A5620
Teratogenic Exposures\|Maternal Phenylketonuria	A5630
Teratogenic Exposures\|Other -teratogenic embryopathy	A5700
Teratogenic Exposures\|Other-antiepileptic embryopathy	A5710
Teratogenic Exposures\|Retinoic acid embryopathy	A5640
Teratogenic Exposures\|Rhesus Disease	A5650
Teratogenic Exposures\|Thalidomide embryopathy	A5660
Teratogenic Exposures\|Toluene embryopathy	A5670
Teratogenic Exposures\|Vitamin A teratogenicity	A5680
Teratogenic Exposures\|Warfarin dysmorphism	A5690
Thorax	THORAX
Thorax\|Agenesis of lung	A5730
Thorax\|Bronchopulmonary sequestration (BPS)	A5740
Thorax\|Chest wall deformity	A5750
Thorax\|Congenital cystic adenomatoid malformation of lung (CCAML)	A5760
Thorax\|Congenital high airway obstruction (CHAOS)	A5770
Thorax\|Diaphragmatic hernia; Congenital (CDH)	A5780
Thorax\|Echogenic lung(s)	A5790
Thorax\|Eventration of diaphragm	A5800
Thorax\|Lung cysts-other	A5810
Thorax\|Other - congenital malformations of lung	A5860
Thorax\|Other congenital malformations of diaphragm	A5870
Thorax\|Pectus carinatum	A5820
Thorax\|Pectus excavatum	A5830
Thorax\|Pleural effusion(s) (hydrothorax)	A5840
Thorax\|Pulmonary hypoplasia	A5850
Twins	TWINS
Twins\|Acardiac twin	A5890
Twins\|Conjoined twins	A5900
Twins\|Dichorionic (DC) twins	A5910
Twins\|Discordant DC twin growth	A5920
Twins\|Discordant MC twin growth	A5930
Twins\|Discordant twin anomaly	A5940
Twins\|Mono-amniotic (MA) twins	A5950
Twins\|Monochorionic diamniotic (MC/DA) twins	A5960
Twins\|Other - malformations of twins	A5980
Twins\|Twin-twin transfusion syndrome (TTTS)	A5970
Unknown	UN

Complications (treatment)
This is important for 145. Complications in the Treatment & pregnancy outcome tab

Options and codes

None	NONE
IVF medication side effect requiring change in intended treatment	ACMP001
Adverse reaction to anaesthetic	ACMP002
Moderate/Severe OHSS requiring paracentesis	ACMP003
Moderate/Severe OHSS requiring culdocentesis	ACMP004
Moderate/Severe OHSS requiring pleural drainage or thoracentesis	ACMP012
OHSS requiring IV hydration	ACMP005
Infection	ACMP006
Hemorrhage requiring blood transfusion	ACMP007
Thromboembolism	ACMP008
Ovarian torsion	ACMP009
Electrolyte disturbance	ACMP013
Kidney problems	ACMP014
Ovarian rupture	ACMP015
Bladder/Bowel injury	ACMP010
Patient death	ACMP011

Country
This is important for 13. Country in the Patient information tab … (Mandatory for Ontario clinics only).

County
This is important for 12. Province in the Patient information tab … (Mandatory for Ontario clinics only).

Options and codes

Alberta	CA-AB
British Columbia	CA-BC
Manitoba	CA-MB
New Brunswick	CA-NB
Newfoundland and Labrador	CA-NL
Northwest Territories	CA-NT
Nova Scotia	CA-NS
Nunavut	CA-NU
Ontario	CA-ON
Prince Edward Island	CA-PE
Quebec	CA-QC
Saskatchewan	CA-SK
Yukon Territory	CA-YT
USA	USA
Out of Province	OUTP
Out of Country	OUTC

Diagnosis codes
The ICD10 code needs to be filled in corresponding with the Record reference code in the CARTR upload specification document provided by BORN.

This is important for

41. Reasons for treatment cycle

Options and codes

Endometriosis	TCR001
Tubal factor	TCR002
Diminished ovarian reserve	TCR003
Male factor	TCR004
No male partner	TCR005
Poly Cystic Ovarian Syndrome (PCOS)	TCR006
Other ovulatory disorders	TCR007
Uterine factor	TCR008
Endocrine disorder	TCR021
Other female factor	TCR009
Gonadotoxic therapy	TCR010
Oocyte banking-for non-cancer/non-medical treatment reasons including donation to commercial egg bank	TCR011
Oocyte banking-cancer and other medical treatment	TCR012
Embryo banking- for non-cancer/non-medical treatment reasons social reasons	TCR013
Embryo banking-cancer and other medical treatment	TCR014
PGT-M/SR for known genetic factor	TCR015
PGT-A	TCR016
Unexplained infertility	TCR017
No female partner	TCR018
Advanced maternal (age 35 or older)	TCR019
Peritoneal factor or severe adhesions	TCR020

42. Reasons for male cycle on the patient information tab.

Options and codes

Aspermia (no semen)	RMF005
Azoospermia	RMF001
Oligozoospermia	RMF002
Oligoasthenoteratozoospermia (OAT)	RMF015
Asthenozoospermia	RMF003
Asthenoteratozoospermia	RMF016
Hypospermia	RMF017
Teratozoospermia	RMF004
Globozoospermia	RMF006
Necrozoospermia	RMF007
High Sperm DNA Fragmentation	RMF008
Retrograde Ejaculation	RMF009
Erectile Dysfunction	RMF010
Sperm Antibodies	RMF011
Klinefelter Syndrome	RMF012
Sperm banking-cancer treatment	RMF014
Known genetic factor	RMF018
Not Specified	RMF013
Other	OTHER

Drugs classification

This is important for:

57. Trigger medication
Option and codes
Other
OTHER
U-hCG
TGM001
Rec-hCG
TGM002
GnRH agonist
TGM003
Rec-hCG + GnRH agonist
TGM004
u-hCG + GnRH agonist
TMG005
None
NONE
Other
OTHER

54. Medication for COS

Option and codes

Clomiphene citrate	COSM001
Aromatase inhibitor	COSM002
OCP	COSM003
Estrogen (e.g., patch, oral)	COSM004
hMG	COSM005
HP-hMG	COSM006
recFSH	COSM007
Ufsh	COSM008
hr-FSH	COSM013
recLH	COSM009
u-hCG	COSM010
rec-hCG	COSM011
Research Study - Information Blinded	COSM012

55. Adjuvant medication

Option and codes

Growth Hormone	ADJ001
DHEA	ADJ002
CoQ10	ADJ003
Steroid (dexamethasone, prednisone, decadron)	ADJ004
Sildenafil	ADJ005
Thyroid medication (topical, patch)	ADJ006
Testosterone patch	ADJ007
Aspirin	ADJ008
Metformin	ADJ009
Dopine Recepter Agonist (cabergoline, dostinex, cabaser)	ADJ010
None	NONE
Other	OTHER

Drug protocol

This is important for 51. Type of stimulation protocol

Option and codes

Natural cycle	SPT001
Modified natural cycle	SPT002
Mild stimulation	SPT003
Antagonist	SPT004
Long agonist	SPT006
Flare agonist	SPT007
Microdose flare agonist	SPT008
IVM protocol	SPT009
Other	OTHER

Freeze method
This is important for 104. Embryo cryo method

There are 3 options:

Slow freezing ECRY001
Vitrification ECRY002
Mixed ECRY003

Slow freezing OOCR001
Vitrification OOCR002
Mixed OOCR003

Gender
This is important to 5. Patient gender

Reason abandoned
This is important for 70. Reason cancelled

Options and codes

Patient illness	CNC001
Patient personal reason	CNC002
Patient error	CNC003
Low ovarian response	CNC004
High ovarian response	CNC005
Premature ovulation	CNC006
Premature luteinization	CNC007
Donor illness	CNC008
Donor personal reason	CNC009
Donor error	CNC010
No access to ovaries	CNC011
Other	OTHER

Reason for no embryo transfer
This is important for 127. Reasons for no ET

Options and codes

No oocytes	NOET001
No utilizable oocytes	NOET002
No normal fertilization	NOET003
No utilizable embryos	NOET004
No sperm	NOET008
Freeze all, OHSS risk	NOET005
Freeze all, PGT-A	NOET009
Freeze all, PGT-M/PGT-SR	NOET010
Freeze all, other reason than OHSS risk or GT	NOET011
Freeze all, other reason than OHSS risk (unknown if PGT)	NOET006
Inadequate uterine lining	NOET007
Patient choice	NOET012

Maternal complications
This is important for 158. Complications of pregnancies and 159. Diabetes and pregnancy

Option and codes

Fetal	FETAL
Fetal \| Anomalies	COP019
Fetal \| Isoimmunization/Alloimmunization	COP001
Fetal \| IUGR	COP002
Fetal \| LGA	COP020
Fetal \| Oligohydramnios	COP003
Fetal \| Polyhydramnios	COP004
Fetal \| Other	COP017
Maternal	MATERNAL
Maternal \| Anemia unresponsive to therapy	COP005
Maternal \| Antepartum Bleeding (Persistent and unexplained)	COP006
Maternal \| Gestational diabetes	COP007
Maternal \| Hyperemesis Gravidarum (Requiring Hospital Admission)	COP008
Maternal \| Hypertensive Disorders in pregnancy	COP009
Placental \| Placenta Abruption	COP010
Placental \| Placenta accreta	COP011
Placental \| Placenta increta	COP012
Placental \| Placenta percreta	COP013
Placental \| Placenta previa	COP014
Maternal \| Preterm labour prior to this admission	COP015
Maternal \| Preterm prelabour premature rupture of membranes (PPROM)	COP016
Placental \| Other	COP018
Maternal \|Prelabour rupture of membranes (PROM)	COP021
Maternal \| Other	COP022
None	NONE
Unknown	UN

Diabetes Complications/Comorbidities	DIAB001
Diabetes Complications/comorbidities \| Nephropathy	DIAB002
Diabetes Complications/comorbidities \| Retinopathy	DIAB003
Gestational	GEST
Gestational \|Insulin	DIAB004
Gestational \|Insulin \| ACE inhibitors	DIAB005
Gestational \|Insulin \| Statins	DIAB006
Gestational \|Insulin \| No Ace Inhibitors or Statins	DIAB019
Gestational \|No Insulin	DIAB007
Gestational \|No Insulin \| No Oral agents	DIAB008
Gestational \|No Insulin \| Oral Antihyperglycemic Agents	DIAB009
Gestational \|Insulin Status Unknown	DIAB020
Type I	DIAB011
Type II	TYPEII
Type II \| Insulin	DIAB012
Type II \| Insulin \| ACE inhibitors	DIAB013
Type II \| Insulin \| Statins	DIAB014
Type II \| Insulin \| No Ace Inhibitors or Statins	DIAB018
Type II \| No Insulin	DIAB015
Type II \| No Insulin \| No Oral Agents	DIAB016
Type II \| No Insulin \| Oral Antihyperglycemic Agents	DIAB017
Type Unknown	DIAB021
Unknown	UN

Drugs, tests and procedures

	Setting the Drugs, test and procedures
1	For all gonadotrophins fill in the associated test “FSH”. To show only the drugs click in the “Type” and click on the icon and then Drug class (gonadotrophin) and the on. Click on to undo the selection.
2	This is important for 125. Preparation of uterine lining
3	This important for 50. level of oocyte provider
4	For every drug the drug classification needs to be filled in. This important for 54. Medication for COS

System options

	Setting the System options
1	The cutoff line needs to be set on 15. This is important for 63/64 # of follicles < or >= 15 mm.

Setting the System options

The cutoff line needs to be set on 15.

This is important for 63/64 # of follicles < or >= 15 mm.

Treatment types

	Setting the treatment types
1	Check if every treatment type is filled in correctly. Note The treatment types are only accessable by Mellowood staff because of security reasons.

Outcome

#	Setting the outcome
1.	Note The Outcome is only accessable by Mellowood staff because of security reasons.

Lists

None

NONE

Abdominal Wall

ABDOM

Abdominal Wall|Bladder exstrophy

A0015

Abdominal Wall|Body stalk anomaly (limb body wall complex)

A0020

Abdominal Wall|Cloacal extrophy

A0030

Abdominal Wall|Gastroschisis

A0040

Abdominal Wall|Limb body wall complex (body stalk anomaly)

A0050

Abdominal Wall|Omphalocele (exomphalos)

A0060

Abdominal Wall|Other - congenital malformations of abdominal wall

A0090

Abdominal Wall|Pentalogy of Cantrell

A0070

Abdominal Wall|Umbilical hernia

A0080

Cardiovascular

CARDIO

Cardiovascular|Aorta - pulmonary window

A0110

Cardiovascular|Aortic arch - double

A0120

Cardiovascular|Aortic arch - interrupted

A0130

Cardiovascular|Aortic atresia

A0140

Cardiovascular|Aortic valve insufficiency

A0150

Cardiovascular|Aortic valve stenosis

A0160

Cardiovascular|Arrhythmia

A0170

Cardiovascular|Atrial fibrillation

A0180

Cardiovascular|Atrial flutter

A0190

Cardiovascular|Atrial septal defect (ASD)

A0200

Cardiovascular|Atrioventricular septal defect (AVSD) (endocardial cushion defect)

A0210

Cardiovascular|Bilateral SVC (superior vena cava)

A0220

Cardiovascular|Bradycardia (bradyarrhythmia)

A0230

Cardiovascular|Cardiac dysfunction

A0240

Cardiovascular|Cardiac tumour / mass

A0250

Cardiovascular|Cardiomegaly

A0260

Cardiovascular|Cardiomyopathy - dilated

A0270

Cardiovascular|Cardiomyopathy - fetus of diabetic mother

A0280

Cardiovascular|Cardiomyopathy - hypertrophic (HOCM)

A0290

Cardiovascular|Coarctation of aorta

A0300

Cardiovascular|Common atrium

A0310

Cardiovascular|Complete Heart Block

A0320

Cardiovascular|Congenital heart block (CHB)

A0330

Cardiovascular|Congenital heart disease

A0340

Cardiovascular|Coronary artery fistula

A0350

Cardiovascular|Dextrocardia

A0360

Cardiovascular|Dilated ascending aorta

A0370

Cardiovascular|Diverticulum - LV

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