Common Anomalies
If any anomaly is selected the default selection will be 1995-2014, Isolated and Singleton
1
All anomalies
17
ALL CHD
44
Ano-rectal atresia and stenosis
29
Aortic valve atresia/stenosis
22
ASD
43
Atresia or stenosis of other parts of small intestine
23
AVSD
102
Cleft lip with or without cleft palate
103
Cleft palate
32
Coarctation of aorta
13
Congenital cataract
55
Congenital hydronephrosis
75
Craniosynostosis
36
Cystic adenomatous malf of lung
48
Diaphragmatic hernia
DS1
Down Syndrome
DS2
Down syndrome with CHD and gastrointestinal anomaly
DS3
Down syndrome with any CHD but not gastrointestinal anomalies
DS4
Down syndrome with any gastrointestinal anomaly but not CHD
DS5
Down syndrome without CHD or gastrointestinal anomaly
42
Duodenal atresia or stenosis
50
Gastroschisis
7
Hydrocephalus
30
Hypoplastic left heart
59
Hypospadias
62
Limb reduction defects�
110
Mitral valve anomalies
54
Multicystic renal dysplasia
41
Oesophageal atresia with or without tracheo-oesophageal fistula
51
Omphalocele
100
PDA as only CHD in term infants (>=37 weeks)
27
Pulmonary valve stenosis
97
Severe CHD
8
Severe microcephaly
6
Spina Bifida
24
Tetralogy of Fallot
19
Transposition of great vessels
21
VSD
Rare Anomalies and Genetic Syndromes
Rare Anomalies and Genetic Syndromes selections are for 1995-2014, singleton and multiple births
aud5
Accessory kidney
aud22
Angelman syndrome
al47
Annular pancreas
aud1
Anomalies of corpus callosum
aud3
Anomalies of intestinal fixation
al12
Anophthalmos
al11
Anophthalmos / microphthalmos
al16
Anotia
al111
Aortic atresia / interrupte aortic arch
al9
Arhinencephaly / holoprosencephaly
aud10
Arthrogryposis multiplex congenita
al46
Atresia of bile ducts
aud20
Beckwith Wiedeman syndrome
aud6
Bladder exstrophy
al35
Choanal atresia
al18
Common arterial truncus
al14
Congenital glaucoma
aud16
Cornelia de Lange syndrome
aud24
Cri-du chat syndrome
aud14
Di George syndrome
al109
Double outlet right ventricle
al26
Ebstein�s anomaly
al91
Edward syndrome/tri 18
al5
Encephalocele
aud7
Epispadia
aud15
Goldenhar syndrome
al45
Hirschsprung�s disease
al31
Hypoplastic right heart
al60
Indeterminate sex
aud25
Karyotype XXX
al93
Klinefelter syndrome
aud17
Noonan syndrome
al90
Patau syndrome/tri 13
aud27
Pierre-Robin sequence
aud8
Posterior urethral valves
aud18
Prader-Willi
aud9
Prune Belly
al28
Pulmonary valve atresia
al20
Single ventricle
al79
Situs inversus
al33
Total anom pulm venous return
al25
Triscuspid atresia and stenosis
al92
Turner syndrome
aud4
Unilateral renal agenesis
al112
VATER/VACTERL
aud21
Williams syndrome
aud23
Wolff-Hirschorn syndrome
Custom Selection
Select anomaly group
Accessory kidney
All anomalies
ALL CHD
Angelman syndrome
Annular pancreas
Anomalies of corpus callosum
Anomalies of intestinal fixation
Anophthalmos
Anophthalmos / microphthalmos
Ano-rectal atresia and stenosis
Anotia
Aortic atresia / interrupte aortic arch
Aortic valve atresia/stenosis
Arhinencephaly / holoprosencephaly
Arthrogryposis multiplex congenita
ASD
Atresia of bile ducts
Atresia or stenosis of other parts of small intestine
AVSD
Beckwith Wiedeman syndrome
Bladder exstrophy
Choanal atresia
Cleft lip with or without cleft palate
Cleft palate
Coarctation of aorta
Common arterial truncus
Congenital cataract
Congenital glaucoma
Congenital hydronephrosis
Cornelia de Lange syndrome
Craniosynostosis
Cri-du chat syndrome
Cystic adenomatous malf of lung
Di George syndrome
Diaphragmatic hernia
Double outlet right ventricle
Down Syndrome
Down syndrome with CHD and gastrointestinal anomaly
Down syndrome with any CHD but not gastrointestinal anomalies
Down syndrome with any gastrointestinal anomaly but not CHD
Down syndrome without CHD or gastrointestinal anomaly
Duodenal atresia or stenosis
Ebstein�s anomaly
Edward syndrome/tri 18
Encephalocele
Epispadia
Gastroschisis
Goldenhar syndrome
Hirschsprung�s disease
Hydrocephalus
Hypoplastic left heart
Hypoplastic right heart
Hypospadias
Indeterminate sex
Karyotype XXX
Klinefelter syndrome
Limb reduction defects�
Mitral valve anomalies
Multicystic renal dysplasia
Noonan syndrome
Oesophageal atresia with or without tracheo-oesophageal fistula
Omphalocele
Patau syndrome/tri 13
PDA as only CHD in term infants (>=37 weeks)
Pierre-Robin sequence
Posterior urethral valves
Prader-Willi
Prune Belly
Pulmonary valve atresia
Pulmonary valve stenosis
Severe CHD
Severe microcephaly
Single ventricle
Situs inversus
Spina Bifida
Tetralogy of Fallot
Total anom pulm venous return
Transposition of great vessels
Triscuspid atresia and stenosis
Turner syndrome
Unilateral renal agenesis
VATER/VACTERL
VSD
Williams syndrome
Wolff-Hirschorn syndrome
Custom Selections - Click on row to remove selection
Include 95% CI
Auto scale Y axis
Smooth line
Enforce same registries in selection (change will clear any selection)
Degree of heterogeneity (I²) medians year 1, years 2-10:
●
moderate (50-75%),
♦
severe (>75%)
i_sq >75 (cross)
i_sq scale marker
i_sq max year 1, max years 2-10
i_sq median and range all years
i_sq 50-75 (spot)
Additional data are available on request
Registry and population details
×