Common Anomalies
Isolated = Isolated anomalies only;
Mult Inc = Isolated and non-isolated anomalies and genetic syndromes.
con
Reference children
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
66
Club foot – talipes equinovarus
32
Coarctation of aorta
13
Congenital cataract
55
Congenital hydronephrosis
75
Craniosynostosis
48
Diaphragmatic hernia
89
Down syndrome
891
Down syndrome with CHD
892
Down syndrome without CHD
42
Duodenal atresia or stenosis
50
Gastroschisis
67
Hip dislocation and/or dyspasia
7
Hydrocephalus
30
Hypoplastic left heart
59
Hypospadias
93
Klinefelter syndrome
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)
68
Polydactyly
27
Pulmonary valve stenosis
97
Severe CHD
8
Severe microcephaly
6
Spina Bifida
69
Syndactyly
24
Tetralogy of Fallot
19
Transposition of great vessels
92
Turner syndrome
21
VSD
Rare Anomalies and Genetic Syndromes
Selections are for Isolated and non-isolated anomalies and genetic syndromes.
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
al5
Encephalocele
aud7
Epispadia
aud15
Goldenhar syndrome
al45
Hirschsprung’s disease
al31
Hypoplastic right heart
al60
Indeterminate sex
aud25
Karyotype XXX
aud17
Noonan syndrome
aud27
Pierre-Robin sequence
aud8
Posterior urethral valves
aud18
Prader-Willi
al28
Pulmonary valve atresia
al20
Single ventricle
al79
Situs inversus
al33
Total anom pulm venous return
al25
Triscuspid atresia and stenosis
aud4
Unilateral renal agenesis
al112
VATER/VACTERL
aud21
Williams syndrome
aud23
Wolff-Hirschorn syndrome
Custom Selection
Isolated = Isolated anomalies only;
Mult Inc = Isolated and non-isolated anomalies and genetic syndromes.
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
Club foot – talipes equinovarus
Coarctation of aorta
Common arterial truncus
Congenital cataract
Congenital glaucoma
Congenital hydronephrosis
Cornelia de Lange syndrome
Craniosynostosis
Cri-du chat syndrome
Di George syndrome
Diaphragmatic hernia
Double outlet right ventricle
Down syndrome
Down syndrome with CHD
Down syndrome without CHD
Duodenal atresia or stenosis
Ebstein’s anomaly
Encephalocele
Epispadia
Gastroschisis
Goldenhar syndrome
Hip dislocation and/or dyspasia
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
PDA as only CHD in term infants (>=37 weeks)
Pierre-Robin sequence
Polydactyly
Posterior urethral valves
Prader-Willi
Pulmonary valve atresia
Pulmonary valve stenosis
Reference children
Severe CHD
Severe microcephaly
Single ventricle
Situs inversus
Spina Bifida
Syndactyly
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
All selections are for the 1995-2014 birth cohort and include both singleton and multiple pregnancies.
Include 95% CI
Degree of heterogeneity (I²) :
●
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
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