Eurocat
Eurocat Northern Netherlands...
Description
Eurocat NNL is a population-based congenital anomaly registry covering Groningen, Friesland and Drenthe from 1981 onwards. All pregnancy outcomes are covered and information is collected on genetic testing, prenatal diagnosis and risk factors via par...
General Design
Data is collected since 1981, but since 1992 parental consent is needed for registration. Since 1997 information is also obtained via parental questionnaires and pharmacy data. Since 2010, information on non responders is also registered....
- Cohort type
Population cohort, Case only, Registry
- Design
Cross-sectional
- Design description
Data is collected since 1981, but since 1992 parental consent is needed for registration. Since 1997 information is also obtained via parental questionnaires and pharmacy data. Since 2010, information on non responders is also registered.
- Collection type
Retrospective
- Start/End year
1981 - ongoing
- Population
Netherlands (the)
- Regions
Drenthe, Friesland, Groningen
- Number of participants
19000
- Number of participants with samples
0
- Age group at inclusion
Infant (0-23 months), Child (2-12 years)
- Main medical condition
- XVII Congenital malformations, deformations and chromosomal abnormalities
- Q20-Q28 Congenital malformations of the circulatory system
- Q25.9 Congenital malformation of great arteries, unspecified
- Q24 Other congenital malformations of heart
- Q20 Congenital malformations of cardiac chambers and connections
- Q20.0 Congenital malformations of cardiac chambers and connections - Common arterial trunk
- Q21.8 Other congenital malformations of cardiac septa
- Q23.2 Congenital mitral stenosis
- Q20.1 Congenital malformations of cardiac chambers and connections - Double outlet right ventricle
- Q20.2 Congenital malformations of cardiac chambers and connections - Double outlet left ventricle
- Q20.3 Congenital malformations of cardiac chambers and connections - Discordant ventriculoarterial connection
- Q20.4 Congenital malformations of cardiac chambers and connections - Double inlet ventricle
- Q22.3 Other congenital malformations of pulmonary valve
- Q20.5 Congenital malformations of cardiac chambers and connections - Discordant atrioventricular connection
- Q20.6 Isomerism of atrial appendages
- Q20.8 Other congenital malformations of cardiac chambers and connections
- Q20.9 Congenital malformation of cardiac chambers and connections, unspecified
- Q21 Congenital malformations of cardiac septa
- Q21.0 Ventricular septal defect
- Q21.1 Atrial septal defect
- Q21.2 Atrioventricular septal defect
- Q21.3 Tetralogy of Fallot
- Q21.4 Aortopulmonary septal defect
- Q21.9 Congenital malformation of cardiac septum, unspecified
- Q22 Congenital malformations of pulmonary and tricuspid valves
- Q22.0 Pulmonary valve atresia
- Q22.1 Congenital pulmonary valve stenosis
- Q22.2 Congenital pulmonary valve insufficiency
- Q22.4 Congenital tricuspid stenosis
- Q22.5 Congenital malformations of pulmonary and tricuspid valves - Ebstein anomaly
- Q22.6 Congenital malformations of pulmonary and tricuspid valves - Hypoplastic right heart syndrome
- Q22.8 Other congenital malformations of tricuspid valve
- Q22.9 Congenital malformation of tricuspid valve, unspecified
- Q23 Congenital malformations of aortic and mitral valves
- Q23.0 Congenital stenosis of aortic valve
- Q23.1 Congenital insufficiency of aortic valve
- Q23.3 Congenital mitral insufficiency
- Q23.4 Congenital malformations of aortic and mitral valves - Hypoplastic left heart syndrome
- Q23.8 Other congenital malformations of aortic and mitral valves
- Q23.9 Congenital malformation of aortic and mitral valves, unspecified
- Q24.0 Other congenital malformations of heart - Dextrocardia
- Q24.1 Other congenital malformations of heart - Laevocardia
- Q24.2 Other congenital malformations of heart - Cor triatriatum
- Q24.3 Other congenital malformations of heart - Pulmonary infundibular stenosis
- Q24.4 Congenital subaortic stenosis
- Q24.5 Malformation of coronary vessels
- Q24.6 Congenital heart block
- Q24.8 Other specified congenital malformations of heart
- Q24.9 Congenital malformation of heart, unspecified
- Q25 Congenital malformations of great arteries
- Q25.0 Congenital malformations of great arteries - Patent ductus arteriosus
- Q25.1 Coarctation of aorta
- Q25.2 Atresia of aorta
- Q25.3 Stenosis of aorta
- Q25.4 Other congenital malformations of aorta
- Q25.5 Atresia of pulmonary artery
- Q25.6 Stenosis of pulmonary artery
- Q25.7 Other congenital malformations of pulmonary artery
- Q25.8 Other congenital malformations of great arteries
- Q26 Congenital malformations of great veins
- Q26.0 Congenital stenosis of vena cava
- Q26.1 Congenital malformations of great veins - Persistent left superior vena cava
- Q26.2 Congenital malformations of great veins - Total anomalous pulmonary venous connection
- Q26.3 Congenital malformations of great veins - Partial anomalous pulmonary venous connection
- Q26.4 Congenital malformations of great veins - Anomalous pulmonary venous connection, unspecified
- Q26.5 Congenital malformations of great veins - Anomalous portal venous connection
- Q26.6 Congenital malformations of great veins - Portal vein-hepatic artery fistula
- Q26.8 Other congenital malformations of great veins
- Q26.9 Congenital malformation of great vein, unspecified
- Q27 Other congenital malformations of peripheral vascular system
- Q27.0 Congenital absence and hypoplasia of umbilical artery
- Q27.1 Congenital renal artery stenosis
- Q27.2 Other congenital malformations of renal artery
- Q27.3 Peripheral arteriovenous malformation
- Q27.4 Congenital phlebectasia
- Q27.8 Other specified congenital malformations of peripheral vascular system
- Q27.9 Congenital malformation of peripheral vascular system, unspecified
- Q28 Other congenital malformations of circulatory system
- Q28.0 Arteriovenous malformation of precerebral vessels
- Q28.1 Other malformations of precerebral vessels
- Q28.2 Arteriovenous malformation of cerebral vessels
- Q28.3 Other malformations of cerebral vessels
- Q28.8 Other specified congenital malformations of circulatory system
- Q28.9 Congenital malformation of circulatory system, unspecified
- Q80-Q89 Other congenital malformations
- Q80.0 Ichthyosis vulgaris
- Q89.9 Congenital malformation, unspecified
- Q83.8 Other congenital malformations of breast
- Q84.2 Other congenital malformations of hair
- Q80 Congenital ichthyosis
- Q81.1 Epidermolysis bullosa letalis
- Q83.9 Congenital malformation of breast, unspecified
- Q84 Other congenital malformations of integument
- Q89.8 Other specified congenital malformations
- Q80.1 X-linked ichthyosis
- Q80.2 Lamellar ichthyosis
- Q80.3 Congenital bullous ichthyosiform erythroderma
- Q80.4 Congenital ichthyosis - Harlequin fetus
- Q80.8 Other congenital ichthyosis
- Q80.9 Congenital ichthyosis, unspecified
- Q81 Epidermolysis bullosa
- Q81.0 Epidermolysis bullosa simplex
- Q89.1 Congenital malformations of adrenal gland
- Q81.2 Epidermolysis bullosa dystrophica
- Q81.8 Other epidermolysis bullosa
- Q81.9 Epidermolysis bullosa, unspecified
- Q82 Other congenital malformations of skin
- Q82.0 Other congenital malformations of skin - Hereditary lymphoedema
- Q82.1 Other congenital malformations of skin - Xeroderma pigmentosum
- Q82.2 Other congenital malformations of skin - Mastocytosis
- Q82.3 Other congenital malformations of skin - Incontinentia pigmenti
- Q82.4 Other congenital malformations of skin - Ectodermal dysplasia (anhidrotic)
- Q82.5 Congenital non-neoplastic naevus
- Q82.8 Other specified congenital malformations of skin
- Q82.9 Congenital malformation of skin, unspecified
- Q83 Congenital malformations of breast
- Q83.0 Congenital absence of breast with absent nipple
- Q83.1 Accessory breast
- Q83.2 Congenital malformations of breast - Absent nipple
- Q83.3 Congenital malformations of breast - Accessory nipple
- Q84.0 Congenital alopecia
- Q84.1 Congenital morphological disturbances of hair, not elsewhere classified
- Q84.3 Other congenital malformations of integument - Anonychia
- Q84.4 Congenital leukonychia
- Q84.5 Other congenital malformations of integument - Enlarged and hypertrophic nails
- Q84.6 Other congenital malformations of nails
- Q84.8 Other specified congenital malformations of integument
- Q84.9 Congenital malformation of integument, unspecified
- Q85 Phakomatoses, not elsewhere classified
- Q85.0 Phakomatoses, not elsewhere classified - Neurofibromatosis (nonmalignant)
- Q85.1 Phakomatoses, not elsewhere classified - Tuberous sclerosis
- Q85.8 Other phakomatoses, not elsewhere classified
- Q85.9 Phakomatoses, not elsewhere classified - Phakomatosis, unspecified
- Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified
- Q86.0 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified - Fetal alcohol syndrome (dysmorphic)
- Q86.1 Fetal hydantoin syndrome
- Q86.2 Dysmorphism due to warfarin
- Q86.8 Other congenital malformation syndromes due to known exogenous causes
- Q87 Other specified congenital malformation syndromes affecting multiple systems
- Q87.0 Congenital malformation syndromes predominantly affecting facial appearance
- Q87.1 Congenital malformation syndromes predominantly associated with short stature
- Q87.2 Congenital malformation syndromes predominantly involving limbs
- Q87.3 Congenital malformation syndromes involving early overgrowth
- Q87.4 Other specified congenital malformation syndromes affecting multiple systems - Marfan syndrome
- Q87.5 Other congenital malformation syndromes with other skeletal changes
- Q87.8 Other specified congenital malformation syndromes, not elsewhere classified
- Q89 Other congenital malformations, not elsewhere classified
- Q89.0 Congenital malformations of spleen
- Q89.2 Congenital malformations of other endocrine glands
- Q89.3 Other congenital malformations, not elsewhere classified - Situs inversus
- Q89.4 Other congenital malformations, not elsewhere classified - Conjoined twins
- Q89.7 Multiple congenital malformations, not elsewhere classified
- Q50-Q56 Congenital malformations of genital organs
- Q52.5 Fusion of labia
- Q54.4 Hypospadias - Congenital chordee
- Q54.8 Other hypospadias
- Q55.1 Hypoplasia of testis and scrotum
- Q50.3 Other congenital malformations of ovary
- Q51 Congenital malformations of uterus and cervix
- Q50 Congenital malformations of ovaries, fallopian tubes and broad ligaments
- Q50.0 Congenital absence of ovary
- Q50.1 Congenital malformations of ovaries, fallopian tubes and broad ligaments - Developmental ovarian cyst
- Q50.2 Congenital torsion of ovary
- Q50.4 Embryonic cyst of fallopian tube
- Q50.5 Embryonic cyst of broad ligament
- Q50.6 Other congenital malformations of fallopian tube and broad ligament
- Q51.0 Agenesis and aplasia of uterus
- Q51.1 Doubling of uterus with doubling of cervix and vagina
- Q51.2 Other doubling of uterus
- Q51.3 Bicornate uterus
- Q51.4 Unicornate uterus
- Q51.5 Agenesis and aplasia of cervix
- Q51.6 Embryonic cyst of cervix
- Q51.7 Congenital fistulae between uterus and digestive and urinary tracts
- Q51.8 Other congenital malformations of uterus and cervix
- Q51.9 Congenital malformation of uterus and cervix, unspecified
- Q52 Other congenital malformations of female genitalia
- Q52.0 Congenital absence of vagina
- Q52.1 Doubling of vagina
- Q52.2 Congenital rectovaginal fistula
- Q52.3 Other congenital malformations of female genitalia - Imperforate hymen
- Q52.4 Other congenital malformations of vagina
- Q52.6 Congenital malformation of clitoris
- Q52.7 Other congenital malformations of vulva
- Q52.8 Other specified congenital malformations of female genitalia
- Q52.9 Congenital malformation of female genitalia, unspecified
- Q53 Undescended testicle
- Q53.0 Undescended testicle - Ectopic testis
- Q53.1 Undescended testicle, unilateral
- Q53.2 Undescended testicle, bilateral
- Q53.9 Undescended testicle, unspecified
- Q54 Hypospadias
- Q54.0 Hypospadias, balanic
- Q54.1 Hypospadias, penile
- Q54.2 Hypospadias, penoscrotal
- Q54.3 Hypospadias, perineal
- Q54.9 Hypospadias, unspecified
- Q55 Other congenital malformations of male genital organs
- Q55.0 Absence and aplasia of testis
- Q55.2 Other congenital malformations of testis and scrotum
- Q55.3 Atresia of vas deferens
- Q55.4 Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate
- Q55.5 Congenital absence and aplasia of penis
- Q55.6 Other congenital malformations of penis
- Q55.8 Other specified congenital malformations of male genital organs
- Q55.9 Congenital malformation of male genital organ, unspecified
- Q56 Indeterminate sex and pseudohermaphroditism
- Q56.0 Indeterminate sex and pseudohermaphroditism - Hermaphroditism, not elsewhere classified
- Q56.1 Male pseudohermaphroditism, not elsewhere classified
- Q56.2 Female pseudohermaphroditism, not elsewhere classified
- Q56.3 Pseudohermaphroditism, unspecified
- Q56.4 Indeterminate sex, unspecified
- Q90-Q99 Chromosomal abnormalities, not elsewhere classified
- Q90 Down syndrome
- Q91.7 Patau syndrome, unspecified
- Q90.0 Down syndrome - Trisomy 21, meiotic nondisjunction
- Q90.1 Down syndrome - Trisomy 21, mosaicism (mitotic nondisjunction)
- Q90.2 Down syndrome - Trisomy 21, translocation
- Q90.9 Down syndrome, unspecified
- Q91 Edwards syndrome and Patau syndrome
- Q91.0 Edwards syndrome and Patau syndrome - Trisomy 18, meiotic nondisjunction
- Q91.1 Edwards syndrome and Patau syndrome - Trisomy 18, mosaicism (mitotic nondisjunction)
- Q91.2 Edwards syndrome and Patau syndrome - Trisomy 18, translocation
- Q91.3 Edwards syndrome, unspecified
- Q91.4 Edwards syndrome and Patau syndrome - Trisomy 13, meiotic nondisjunction
- Q91.5 Edwards syndrome and Patau syndrome - Trisomy 13, mosaicism (mitotic nondisjunction)
- Q91.6 Edwards syndrome and Patau syndrome - Trisomy 13, translocation
- Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified
- Q92.0 Other trisomies and partial trisomies of the autosomes, not elsewhere classified - Whole chromosome trisomy, meiotic nondisjunction
- Q95.8 Other balanced rearrangements and structural markers
- Q93.4 Monosomies and deletions from the autosomes, not elsewhere classified - Deletion of short arm of chromosome 5
- Q93.5 Other deletions of part of a chromosome
- Q92.1 Other trisomies and partial trisomies of the autosomes, not elsewhere classified - Whole chromosome trisomy, mosaicism (mitotic nondisjunction)
- Q92.2 Major partial trisomy
- Q92.3 Minor partial trisomy
- Q92.4 Other trisomies and partial trisomies of the autosomes, not elsewhere classified - Duplications seen only at prometaphase
- Q92.5 Duplications with other complex rearrangements
- Q92.6 Other trisomies and partial trisomies of the autosomes, not elsewhere classified - Extra marker chromosomes
- Q92.7 Triploidy and polyploidy
- Q92.8 Other specified trisomies and partial trisomies of autosomes
- Q92.9 Trisomy and partial trisomy of autosomes, unspecified
- Q93 Monosomies and deletions from the autosomes, not elsewhere classified
- Q93.0 Monosomies and deletions from the autosomes, not elsewhere classified - Whole chromosome monosomy, meiotic nondisjunction
- Q93.1 Monosomies and deletions from the autosomes, not elsewhere classified - Whole chromosome monosomy, mosaicism (mitotic nondisjunction)
- Q93.2 Monosomies and deletions from the autosomes, not elsewhere classified - Chromosome replaced with ring or dicentric
- Q93.3 Monosomies and deletions from the autosomes, not elsewhere classified - Deletion of short arm of chromosome 4
- Q93.6 Deletions seen only at prometaphase
- Q93.7 Deletions with other complex rearrangements
- Q93.8 Other deletions from the autosomes
- Q93.9 Deletion from autosomes, unspecified
- Q95 Balanced rearrangements and structural markers, not elsewhere classified
- Q95.0 Balanced translocation and insertion in normal individual
- Q95.1 Balanced rearrangements and structural markers, not elsewhere classified - Chromosome inversion in normal individual
- Q95.2 Balanced autosomal rearrangement in abnormal individual
- Q95.3 Balanced sex/autosomal rearrangement in abnormal individual
- Q95.4 Balanced rearrangements and structural markers, not elsewhere classified - Individuals with marker heterochromatin
- Q95.5 Balanced rearrangements and structural markers, not elsewhere classified - Individuals with autosomal fragile site
- Q95.9 Balanced rearrangement and structural marker, unspecified
- Q96 Turner syndrome
- Q96.0 Turner syndrome - Karyotype 45,X
- Q96.1 Turner syndrome - Karyotype 46,X iso (Xq)
- Q96.2 Turner syndrome - Karyotype 46,X with abnormal sex chromosome, except iso (Xq)
- Q96.3 Turner syndrome - Mosaicism, 45,X/46,XX or XY
- Q96.4 Turner syndrome - Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome
- Q96.8 Other variants of Turner syndrome
- Q96.9 Turner syndrome, unspecified
- Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified
- Q97.0 Other sex chromosome abnormalities, female phenotype, not elsewhere classified - Karyotype 47,XXX
- Q97.1 Female with more than three X chromosomes
- Q97.2 Mosaicism, lines with various numbers of X chromosomes
- Q97.3 Female with 46,XY karyotype
- Q97.8 Other specified sex chromosome abnormalities, female phenotype
- Q97.9 Sex chromosome abnormality, female phenotype, unspecified
- Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified
- Q98.0 Other sex chromosome abnormalities, male phenotype, not elsewhere classified - Klinefelter syndrome karyotype 47,XXY
- Q98.1 Klinefelter syndrome, male with more than two X chromosomes
- Q98.2 Klinefelter syndrome, male with 46,XX karyotype
- Q98.3 Other male with 46,XX karyotype
- Q98.4 Other sex chromosome abnormalities, male phenotype, not elsewhere classified - Klinefelter syndrome, unspecified
- Q98.5 Other sex chromosome abnormalities, male phenotype, not elsewhere classified - Karyotype 47,XYY
- Q98.6 Male with structurally abnormal sex chromosome
- Q98.7 Male with sex chromosome mosaicism
- Q98.8 Other specified sex chromosome abnormalities, male phenotype
- Q98.9 Sex chromosome abnormality, male phenotype, unspecified
- Q99 Other chromosome abnormalities, not elsewhere classified
- Q99.0 Other chromosome abnormalities, not elsewhere classified - Chimera 46,XX/46,XY
- Q99.1 Other chromosome abnormalities, not elsewhere classified - 46,XX true hermaphrodite
- Q99.2 Fragile X chromosome
- Q99.8 Other specified chromosome abnormalities
- Q99.9 Other chromosome abnormalities, not elsewhere classified - Chromosomal abnormality, unspecified
- Q00-Q07 Congenital malformations of the nervous system
- Q00 Anencephaly and similar malformations
- Q06.3 Other congenital cauda equina malformations
- Q00.0 Anencephaly
- Q00.1 Anencephaly and similar malformations - Craniorachischisis
- Q00.2 Anencephaly and similar malformations - Iniencephaly
- Q01 Encephalocele
- Q01.0 Frontal encephalocele
- Q01.1 Nasofrontal encephalocele
- Q01.2 Occipital encephalocele
- Q01.8 Encephalocele of other sites
- Q01.9 Encephalocele, unspecified
- Q02 Microcephaly
- Q03 Congenital hydrocephalus
- Q03.0 Congenital hydrocephalus - Malformations of aqueduct of Sylvius
- Q03.1 Congenital hydrocephalus - Atresia of foramina of Magendie and Luschka
- Q03.8 Other congenital hydrocephalus
- Q03.9 Congenital hydrocephalus, unspecified
- Q04 Other congenital malformations of brain
- Q04.0 Congenital malformations of corpus callosum
- Q04.1 Other congenital malformations of brain - Arhinencephaly
- Q04.2 Other congenital malformations of brain - Holoprosencephaly
- Q04.3 Other reduction deformities of brain
- Q04.4 Other congenital malformations of brain - Septo-optic dysplasia
- Q04.5 Other congenital malformations of brain - Megalencephaly
- Q04.6 Congenital cerebral cysts
- Q04.8 Other specified congenital malformations of brain
- Q04.9 Congenital malformation of brain, unspecified
- Q05 Spina bifida
- Q05.0 Cervical spina bifida with hydrocephalus
- Q05.1 Thoracic spina bifida with hydrocephalus
- Q05.2 Lumbar spina bifida with hydrocephalus
- Q05.3 Sacral spina bifida with hydrocephalus
- Q05.4 Unspecified spina bifida with hydrocephalus
- Q05.5 Cervical spina bifida without hydrocephalus
- Q05.6 Thoracic spina bifida without hydrocephalus
- Q05.7 Lumbar spina bifida without hydrocephalus
- Q05.8 Sacral spina bifida without hydrocephalus
- Q05.9 Spina bifida, unspecified
- Q06 Other congenital malformations of spinal cord
- Q06.0 Other congenital malformations of spinal cord - Amyelia
- Q06.1 Hypoplasia and dysplasia of spinal cord
- Q06.2 Other congenital malformations of spinal cord - Diastematomyelia
- Q06.4 Other congenital malformations of spinal cord - Hydromyelia
- Q06.8 Other specified congenital malformations of spinal cord
- Q06.9 Congenital malformation of spinal cord, unspecified
- Q07 Other congenital malformations of nervous system
- Q07.0 Other congenital malformations of nervous system - Arnold-Chiari syndrome
- Q07.8 Other specified congenital malformations of nervous system
- Q07.9 Congenital malformation of nervous system, unspecified
- Q35-Q37 Cleft lip and cleft palate
- Q37.9 Unspecified cleft palate with unilateral cleft lip
- Q37 Cleft palate with cleft lip
- Q37.8 Unspecified cleft palate with bilateral cleft lip
- Q37.1 Cleft hard palate with unilateral cleft lip
- Q35 Cleft palate
- Q35.1 Cleft hard palate
- Q35.3 Cleft soft palate
- Q35.5 Cleft hard palate with cleft soft palate
- Q35.7 Cleft uvula
- Q35.9 Cleft palate, unspecified
- Q36 Cleft lip
- Q36.0 Cleft lip, bilateral
- Q36.1 Cleft lip, median
- Q36.9 Cleft lip, unilateral
- Q37.0 Cleft hard palate with bilateral cleft lip
- Q37.2 Cleft soft palate with bilateral cleft lip
- Q37.3 Cleft soft palate with unilateral cleft lip
- Q37.4 Cleft hard and soft palate with bilateral cleft lip
- Q37.5 Cleft hard and soft palate with unilateral cleft lip
- Q30-Q34 Congenital malformations of the respiratory system
- Q33.5 Ectopic tissue in lung
- Q30 Congenital malformations of nose
- Q30.0 Congenital malformations of nose - Choanal atresia
- Q30.1 Agenesis and underdevelopment of nose
- Q30.2 Fissured, notched and cleft nose
- Q30.3 Congenital perforated nasal septum
- Q30.8 Other congenital malformations of nose
- Q30.9 Congenital malformation of nose, unspecified
- Q31 Congenital malformations of larynx
- Q31.0 Web of larynx
- Q31.1 Congenital subglottic stenosis
- Q31.2 Congenital malformations of larynx - Laryngeal hypoplasia
- Q31.3 Congenital malformations of larynx - Laryngocele
- Q31.5 Congenital laryngomalacia
- Q31.8 Other congenital malformations of larynx
- Q31.9 Congenital malformation of larynx, unspecified
- Q32 Congenital malformations of trachea and bronchus
- Q32.0 Congenital tracheomalacia
- Q32.1 Other congenital malformations of trachea
- Q32.2 Congenital bronchomalacia
- Q32.3 Congenital stenosis of bronchus
- Q32.4 Other congenital malformations of bronchus
- Q33 Congenital malformations of lung
- Q33.0 Congenital cystic lung
- Q33.1 Accessory lobe of lung
- Q33.2 Sequestration of lung
- Q33.3 Agenesis of lung
- Q33.4 Congenital bronchiectasis
- Q33.6 Hypoplasia and dysplasia of lung
- Q33.8 Other congenital malformations of lung
- Q33.9 Congenital malformation of lung, unspecified
- Q34 Other congenital malformations of respiratory system
- Q34.0 Anomaly of pleura
- Q34.1 Congenital cyst of mediastinum
- Q34.8 Other specified congenital malformations of respiratory system
- Q34.9 Congenital malformation of respiratory system, unspecified
- Q10-Q18 Congenital malformations of eye, ear, face and neck
- Q17.9 Congenital malformation of ear, unspecified
- Q10 Congenital malformations of eyelid, lacrimal apparatus and orbit
- Q10.0 Congenital ptosis
- Q10.1 Congenital ectropion
- Q10.2 Congenital entropion
- Q10.3 Other congenital malformations of eyelid
- Q10.4 Absence and agenesis of lacrimal apparatus
- Q10.5 Congenital stenosis and stricture of lacrimal duct
- Q17.8 Other specified congenital malformations of ear
- Q10.6 Other congenital malformations of lacrimal apparatus
- Q10.7 Congenital malformation of orbit
- Q11 Anophthalmos, microphthalmos and macrophthalmos
- Q11.0 Anophthalmos, microphthalmos and macrophthalmos - Cystic eyeball
- Q11.1 Other anophthalmos
- Q11.2 Microphthalmos
- Q11.3 Macrophthalmos
- Q12 Congenital lens malformations
- Q12.0 Congenital cataract
- Q12.1 Congenital displaced lens
- Q12.2 Coloboma of lens
- Q12.3 Congenital aphakia
- Q12.4 Congenital lens malformations - Spherophakia
- Q12.8 Other congenital lens malformations
- Q12.9 Congenital lens malformation, unspecified
- Q13 Congenital malformations of anterior segment of eye
- Q13.0 Coloboma of iris
- Q13.1 Absence of iris
- Q13.2 Other congenital malformations of iris
- Q13.3 Congenital corneal opacity
- Q13.4 Other congenital corneal malformations
- Q13.5 Congenital malformations of anterior segment of eye - Blue sclera
- Q13.8 Other congenital malformations of anterior segment of eye
- Q13.9 Congenital malformation of anterior segment of eye, unspecified
- Q14 Congenital malformations of posterior segment of eye
- Q14.0 Congenital malformation of vitreous humour
- Q14.1 Congenital malformation of retina
- Q14.2 Congenital malformation of optic disc
- Q14.3 Congenital malformation of choroid
- Q14.8 Other congenital malformations of posterior segment of eye
- Q14.9 Congenital malformation of posterior segment of eye, unspecified
- Q15 Other congenital malformations of eye
- Q15.0 Congenital glaucoma
- Q15.8 Other specified congenital malformations of eye
- Q15.9 Congenital malformation of eye, unspecified
- Q16 Congenital malformations of ear causing impairment of hearing
- Q16.0 Congenital absence of (ear) auricle
- Q16.1 Congenital absence, atresia and stricture of auditory canal (external)
- Q16.2 Absence of eustachian tube
- Q16.3 Congenital malformation of ear ossicles
- Q16.4 Other congenital malformations of middle ear
- Q16.5 Congenital malformation of inner ear
- Q16.9 Congenital malformation of ear causing impairment of hearing, unspecified
- Q17 Other congenital malformations of ear
- Q17.0 Other congenital malformations of ear - Accessory auricle
- Q17.1 Other congenital malformations of ear - Macrotia
- Q17.2 Other congenital malformations of ear - Microtia
- Q17.3 Other misshapen ear
- Q17.4 Misplaced ear
- Q17.5 Prominent ear
- Q18 Other congenital malformations of face and neck
- Q18.0 Sinus, fistula and cyst of branchial cleft
- Q18.1 Preauricular sinus and cyst
- Q18.2 Other branchial cleft malformations
- Q18.3 Webbing of neck
- Q18.4 Other congenital malformations of face and neck - Macrostomia
- Q18.5 Other congenital malformations of face and neck - Microstomia
- Q18.6 Other congenital malformations of face and neck - Macrocheilia
- Q18.7 Other congenital malformations of face and neck - Microcheilia
- Q18.8 Other specified congenital malformations of face and neck
- Q18.9 Congenital malformation of face and neck, unspecified
- Q38-Q45 Other congenital malformations of the digestive system
- Q43 Other congenital malformations of intestine
- Q38 Other congenital malformations of tongue, mouth and pharynx
- Q38.0 Congenital malformations of lips, not elsewhere classified
- Q38.1 Other congenital malformations of tongue, mouth and pharynx - Ankyloglossia
- Q38.2 Other congenital malformations of tongue, mouth and pharynx - Macroglossia
- Q38.3 Other congenital malformations of tongue
- Q38.4 Congenital malformations of salivary glands and ducts
- Q38.5 Congenital malformations of palate, not elsewhere classified
- Q38.6 Other congenital malformations of mouth
- Q38.7 Other congenital malformations of tongue, mouth and pharynx - Pharyngeal pouch
- Q38.8 Other congenital malformations of pharynx
- Q39 Congenital malformations of oesophagus
- Q39.0 Atresia of oesophagus without fistula
- Q39.1 Atresia of oesophagus with tracheo-oesophageal fistula
- Q39.2 Congenital tracheo-oesophageal fistula without atresia
- Q39.3 Congenital stenosis and stricture of oesophagus
- Q39.4 Congenital malformations of oesophagus - Oesophageal web
- Q39.5 Congenital dilatation of oesophagus
- Q39.6 Diverticulum of oesophagus
- Q39.8 Other congenital malformations of oesophagus
- Q39.9 Congenital malformation of oesophagus, unspecified
- Q40 Other congenital malformations of upper alimentary tract
- Q40.0 Congenital hypertrophic pyloric stenosis
- Q40.1 Congenital hiatus hernia
- Q40.2 Other specified congenital malformations of stomach
- Q40.3 Congenital malformation of stomach, unspecified
- Q40.8 Other specified congenital malformations of upper alimentary tract
- Q40.9 Congenital malformation of upper alimentary tract, unspecified
- Q41 Congenital absence, atresia and stenosis of small intestine
- Q41.0 Congenital absence, atresia and stenosis of duodenum
- Q41.1 Congenital absence, atresia and stenosis of jejunum
- Q41.2 Congenital absence, atresia and stenosis of ileum
- Q41.8 Congenital absence, atresia and stenosis of other specified parts of small intestine
- Q41.9 Congenital absence, atresia and stenosis of small intestine, part unspecified
- Q42 Congenital absence, atresia and stenosis of large intestine
- Q42.0 Congenital absence, atresia and stenosis of rectum with fistula
- Q42.1 Congenital absence, atresia and stenosis of rectum without fistula
- Q42.2 Congenital absence, atresia and stenosis of anus with fistula
- Q42.3 Congenital absence, atresia and stenosis of anus without fistula
- Q42.8 Congenital absence, atresia and stenosis of other parts of large intestine
- Q42.9 Congenital absence, atresia and stenosis of large intestine, part unspecified
- Q43.0 Other congenital malformations of intestine - Meckel diverticulum
- Q43.1 Other congenital malformations of intestine - Hirschsprung disease
- Q43.2 Other congenital functional disorders of colon
- Q43.3 Congenital malformations of intestinal fixation
- Q43.4 Duplication of intestine
- Q43.5 Other congenital malformations of intestine - Ectopic anus
- Q43.6 Congenital fistula of rectum and anus
- Q43.7 Other congenital malformations of intestine - Persistent cloaca
- Q43.8 Other specified congenital malformations of intestine
- Q43.9 Congenital malformation of intestine, unspecified
- Q44 Congenital malformations of gallbladder, bile ducts and liver
- Q44.0 Agenesis, aplasia and hypoplasia of gallbladder
- Q44.1 Other congenital malformations of gallbladder
- Q44.2 Atresia of bile ducts
- Q44.3 Congenital stenosis and stricture of bile ducts
- Q44.4 Congenital malformations of gallbladder, bile ducts and liver - Choledochal cyst
- Q44.5 Other congenital malformations of bile ducts
- Q44.6 Cystic disease of liver
- Q44.7 Other congenital malformations of liver
- Q45 Other congenital malformations of digestive system
- Q45.0 Agenesis, aplasia and hypoplasia of pancreas
- Q45.1 Other congenital malformations of digestive system - Annular pancreas
- Q45.2 Congenital pancreatic cyst
- Q45.3 Other congenital malformations of pancreas and pancreatic duct
- Q45.8 Other specified congenital malformations of digestive system
- Q45.9 Congenital malformation of digestive system, unspecified
- Q60-Q64 Congenital malformations of the urinary system
- Q60.3 Renal hypoplasia, unilateral
- Q60 Renal agenesis and other reduction defects of kidney
- Q60.0 Renal agenesis, unilateral
- Q60.1 Renal agenesis, bilateral
- Q60.2 Renal agenesis, unspecified
- Q60.4 Renal hypoplasia, bilateral
- Q60.5 Renal hypoplasia, unspecified
- Q60.6 Renal agenesis and other reduction defects of kidney - Potter syndrome
- Q61 Cystic kidney disease
- Q61.0 Cystic kidney disease - Congenital single renal cyst
- Q61.1 Polycystic kidney, autosomal recessive
- Q61.2 Polycystic kidney, autosomal dominant
- Q61.3 Polycystic kidney, unspecified
- Q61.4 Cystic kidney disease - Renal dysplasia
- Q61.5 Medullary cystic kidney
- Q61.8 Other cystic kidney diseases
- Q61.9 Cystic kidney disease, unspecified
- Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter
- Q62.0 Congenital hydronephrosis
- Q62.1 Atresia and stenosis of ureter
- Q62.2 Congenital megaloureter
- Q62.3 Other obstructive defects of renal pelvis and ureter
- Q62.4 Agenesis of ureter
- Q62.5 Duplication of ureter
- Q62.6 Malposition of ureter
- Q62.7 Congenital vesico-uretero-renal reflux
- Q62.8 Other congenital malformations of ureter
- Q63 Other congenital malformations of kidney
- Q63.0 Accessory kidney
- Q63.1 Lobulated, fused and horseshoe kidney
- Q63.2 Ectopic kidney
- Q63.3 Hyperplastic and giant kidney
- Q63.8 Other specified congenital malformations of kidney
- Q63.9 Congenital malformation of kidney, unspecified
- Q64 Other congenital malformations of urinary system
- Q64.0 Other congenital malformations of urinary system - Epispadias
- Q64.1 Exstrophy of urinary bladder
- Q64.2 Congenital posterior urethral valves
- Q64.3 Other atresia and stenosis of urethra and bladder neck
- Q64.4 Malformation of urachus
- Q64.5 Congenital absence of bladder and urethra
- Q64.6 Congenital diverticulum of bladder
- Q64.7 Other congenital malformations of bladder and urethra
- Q64.8 Other specified congenital malformations of urinary system
- Q64.9 Congenital malformation of urinary system, unspecified
- Q65-Q79 Congenital malformations and deformations of the musculoskeletal system
- Q65 Congenital deformities of hip
- Q65.0 Congenital dislocation of hip, unilateral
- Q65.1 Congenital dislocation of hip, bilateral
- Q65.2 Congenital dislocation of hip, unspecified
- Q65.3 Congenital subluxation of hip, unilateral
- Q65.4 Congenital subluxation of hip, bilateral
- Q65.5 Congenital subluxation of hip, unspecified
- Q65.6 Unstable hip
- Q65.8 Other congenital deformities of hip
- Q65.9 Congenital deformity of hip, unspecified
- Q66 Congenital deformities of feet
- Q66.0 Congenital deformities of feet - Talipes equinovarus
- Q66.1 Congenital deformities of feet - Talipes calcaneovarus
- Q66.2 Congenital deformities of feet - Metatarsus varus
- Q66.3 Other congenital varus deformities of feet
- Q66.4 Congenital deformities of feet - Talipes calcaneovalgus
- Q66.5 Congenital pes planus
- Q66.6 Other congenital valgus deformities of feet
- Q66.7 Congenital deformities of feet - Pes cavus
- Q66.8 Other congenital deformities of feet
- Q66.9 Congenital deformity of feet, unspecified
- Q67 Congenital musculoskeletal deformities of head, face, spine and chest
- Q67.0 Congenital musculoskeletal deformities of head, face, spine and chest - Facial asymmetry
- Q67.1 Congenital musculoskeletal deformities of head, face, spine and chest - Compression facies
- Q67.2 Congenital musculoskeletal deformities of head, face, spine and chest - Dolichocephaly
- Q67.3 Congenital musculoskeletal deformities of head, face, spine and chest - Plagiocephaly
- Q67.4 Other congenital deformities of skull, face and jaw
- Q67.5 Congenital deformity of spine
- Q67.6 Congenital musculoskeletal deformities of head, face, spine and chest - Pectus excavatum
- Q67.7 Congenital musculoskeletal deformities of head, face, spine and chest - Pectus carinatum
- Q67.8 Other congenital deformities of chest
- Q68 Other congenital musculoskeletal deformities
- Q68.0 Congenital deformity of sternocleidomastoid muscle
- Q68.1 Congenital deformity of hand
- Q68.2 Congenital deformity of knee
- Q68.3 Congenital bowing of femur
- Q68.4 Congenital bowing of tibia and fibula
- Q68.5 Congenital bowing of long bones of leg, unspecified
- Q68.8 Other specified congenital musculoskeletal deformities
- Q69 Polydactyly
- Q69.0 Polydactyly - Accessory finger(s)
- Q69.1 Polydactyly - Accessory thumb(s)
- Q69.2 Polydactyly - Accessory toe(s)
- Q69.9 Polydactyly, unspecified
- Q70 Syndactyly
- Q70.0 Syndactyly - Fused fingers
- Q70.1 Syndactyly - Webbed fingers
- Q70.2 Syndactyly - Fused toes
- Q70.3 Syndactyly - Webbed toes
- Q70.4 Polysyndactyly
- Q70.9 Syndactyly, unspecified
- Q71 Reduction defects of upper limb
- Q71.0 Congenital complete absence of upper limb(s)
- Q71.1 Congenital absence of upper arm and forearm with hand present
- Q71.2 Congenital absence of both forearm and hand
- Q71.3 Congenital absence of hand and finger(s)
- Q71.4 Longitudinal reduction defect of radius
- Q71.5 Longitudinal reduction defect of ulna
- Q71.6 Reduction defects of upper limb - Lobster-claw hand
- Q71.8 Other reduction defects of upper limb(s)
- Q71.9 Reduction defect of upper limb, unspecified
- Q72 Reduction defects of lower limb
- Q78 Other osteochondrodysplasias
- Q72.0 Congenital complete absence of lower limb(s)
- Q72.1 Congenital absence of thigh and lower leg with foot present
- Q72.2 Congenital absence of both lower leg and foot
- Q72.3 Congenital absence of foot and toe(s)
- Q72.4 Longitudinal reduction defect of femur
- Q72.5 Longitudinal reduction defect of tibia
- Q72.6 Longitudinal reduction defect of fibula
- Q72.7 Reduction defects of lower limb - Split foot
- Q72.8 Other reduction defects of lower limb(s)
- Q72.9 Reduction defect of lower limb, unspecified
- Q73 Reduction defects of unspecified limb
- Q73.0 Congenital absence of unspecified limb(s)
- Q73.1 Phocomelia, unspecified limb(s)
- Q73.8 Other reduction defects of unspecified limb(s)
- Q74 Other congenital malformations of limb(s)
- Q74.0 Other congenital malformations of upper limb(s), including shoulder girdle
- Q74.1 Congenital malformation of knee
- Q74.2 Other congenital malformations of lower limb(s), including pelvic girdle
- Q74.3 Other congenital malformations of limb(s) - Arthrogryposis multiplex congenita
- Q74.8 Other specified congenital malformations of limb(s)
- Q74.9 Unspecified congenital malformation of limb(s)
- Q75 Other congenital malformations of skull and face bones
- Q75.0 Other congenital malformations of skull and face bones - Craniosynostosis
- Q75.1 Craniofacial dysostosis
- Q75.2 Other congenital malformations of skull and face bones - Hypertelorism
- Q75.3 Other congenital malformations of skull and face bones - Macrocephaly
- Q75.4 Mandibulofacial dysostosis
- Q75.5 Oculomandibular dysostosis
- Q75.8 Other specified congenital malformations of skull and face bones
- Q75.9 Congenital malformation of skull and face bones, unspecified
- Q76 Congenital malformations of spine and bony thorax
- Q76.0 Congenital malformations of spine and bony thorax - Spina bifida occulta
- Q76.1 Congenital malformations of spine and bony thorax - Klippel-Feil syndrome
- Q76.2 Congenital spondylolisthesis
- Q76.3 Congenital scoliosis due to congenital bony malformation
- Q76.4 Other congenital malformations of spine, not associated with scoliosis
- Q76.5 Congenital malformations of spine and bony thorax - Cervical rib
- Q76.6 Other congenital malformations of ribs
- Q76.7 Congenital malformation of sternum
- Q76.8 Other congenital malformations of bony thorax
- Q76.9 Congenital malformation of bony thorax, unspecified
- Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine
- Q77.0 Osteochondrodysplasia with defects of growth of tubular bones and spine - Achondrogenesis
- Q77.1 Osteochondrodysplasia with defects of growth of tubular bones and spine - Thanatophoric short stature
- Q78.4 Other osteochondrodysplasias - Enchondromatosis
- Q77.2 Osteochondrodysplasia with defects of growth of tubular bones and spine - Short rib syndrome
- Q77.3 Osteochondrodysplasia with defects of growth of tubular bones and spine - Chondrodysplasia punctata
- Q77.4 Osteochondrodysplasia with defects of growth of tubular bones and spine - Achondroplasia
- Q77.5 Osteochondrodysplasia with defects of growth of tubular bones and spine - Dystrophic dysplasia
- Q77.6 Osteochondrodysplasia with defects of growth of tubular bones and spine - Chondroectodermal dysplasia
- Q77.7 Osteochondrodysplasia with defects of growth of tubular bones and spine - Spondyloepiphyseal dysplasia
- Q77.8 Other osteochondrodysplasia with defects of growth of tubular bones and spine
- Q77.9 Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified
- Q78.0 Other osteochondrodysplasias - Osteogenesis imperfecta
- Q78.1 Other osteochondrodysplasias - Polyostotic fibrous dysplasia
- Q78.2 Other osteochondrodysplasias - Osteopetrosis
- Q78.3 Other osteochondrodysplasias - Progressive diaphyseal dysplasia
- Q78.5 Other osteochondrodysplasias - Metaphyseal dysplasia
- Q78.6 Other osteochondrodysplasias - Multiple congenital exostoses
- Q78.8 Other specified osteochondrodysplasias
- Q78.9 Other osteochondrodysplasias - Osteochondrodysplasia, unspecified
- Q79 Congenital malformations of the musculoskeletal system, not elsewhere classified
- Q79.0 Congenital diaphragmatic hernia
- Q79.1 Other congenital malformations of diaphragm
- Q79.2 Congenital malformations of the musculoskeletal system, not elsewhere classified - Exomphalos
- Q79.3 Congenital malformations of the musculoskeletal system, not elsewhere classified - Gastroschisis
- Q79.4 Congenital malformations of the musculoskeletal system, not elsewhere classified - Prune belly syndrome
- Q79.5 Other congenital malformations of abdominal wall
- Q79.6 Congenital malformations of the musculoskeletal system, not elsewhere classified - Ehlers-Danlos syndrome
- Q79.8 Other congenital malformations of musculoskeletal system
- Q79.9 Congenital malformation of musculoskeletal system, unspecified
- PID
https://doi.org/10.34760/5f5b80ff2a7a4
Contact and Contributors
- dr. HEK (Hermien) de Walleh.e.k.de.walle@umcg.nl
- dr. MK (Marian) Bakkerm.k.bakker@umcg.nl
- dr. JEH (Jorieke) van Kammen-Bergmanj.e.h.van.kammen@umcg.nl
Available Data & Samples
Data categories
- Survey data
- Medical records
- Other
Areas of information
- Socio-demographic and economic characteristics
- Age/birthdate
- Sex/gender
- Twin
- Residence
- Birthplace
- Education
- Labour force and retirement
- Non-pharmacological interventions
- Surgical interventions
- Radiological interventions
- Radiotherapy interventions
- Death
- Vital status
- Physical measures and assessments
- Physical characteristics
- Anthropometry
- Circulation and respiration
- Muscles, skeleton and mobility
- Sensory and pain
- Brain and nerves
- Skin and subcutaneous tissue
- Other physical measures and assessments
- Cognition, personality and psychological measures and assessments
- Cognitive functioning
- Administrative information
- Identifiers
- Questionnaire and interview-related information
- Date and time-related information
- Other administrative information
- Lifestyle and behaviours
- Tobacco
- Alcohol
- Drugs
- Other and unspecified lifestyle information
- Medication and supplements
- Medication and supplement intake
- Birth, pregnancy and reproductive health history
- Pregnancy, delivery and birth
- Fertility and sexual health
Subpopulations
List of subcohorts or subpopulations for this resource...
| Name | Description | Number of participants |
|---|
Collection events
List of collection events defined for this resource...
| Name | Description | Participants | Start end year |
|---|
Networks
Networks Explanation about networks from this cohort and the functionality seen here....
Access conditions
- Conditions
disease specific research
Funding & Citation requirements
- Funding
Eurocat NNL is funded by the Netherlands Ministry of Public Health, Welfare and Sports (VWS)
- Citation requirements
VWS should be acknowledged, as well as the parents and children who agreed to have their data registered in the EUROCAT NNL database.