Waardelijst ProbleemNaam_AangeborenAfwijkingenSyndromen 2018‑08‑10 02:17:56

Id 2.16.840.1.113883.2.4.3.11.60.90.77.11.222 Ingangsdatum 2018‑08‑10 02:17:56 Status Definitief Versielabel Naam ProbleemNaam_AangeborenAfwijkingenSyndromen Weergavenaam ProbleemNaam_AangeborenAfwijkingenSyndromen Copyright This artefact includes content from SNOMED Clinical Terms® (SNOMED CT®) which is copyright of the International Health Terminology Standards Development Organisation (IHTSDO). Implementers of these artefacts must have the appropriate SNOMED CT Affiliate license - for more information contact http://www.snomed.org/snomed-ct/getsnomed-ct or info@snomed.org. 2 bron codesystemen 2.16.840.1.113883.6.96 - SNOMED CT - urn:oid:2.16.840.1.113883.6.96 2.16.840.1.113883.2.4.4.13.8 - CongenitaleAfwijkingen - urn:oid:2.16.840.1.113883.2.4.4.13.8 Alles uitklappenAlles inklappen Niveau/ Type Code Weergavenaam Codesysteem Benamingen Omschrijving 0‑A 88425004 Congenital anomaly of nervous system (disorder) SNOMED CT Aangeboren afwijkingen centraal zenuwstelsel 1‑L 89369001 Anencephalus (disorder) SNOMED CT 1‑L 414667000 Meningomyelocele (disorder) SNOMED CT 1‑L 30023002 Hydranencephaly (disorder) SNOMED CT 1‑L 47032000 Congenital hydrocephalus (disorder) SNOMED CT 1‑L 30915001 Holoprosencephaly sequence (disorder) SNOMED CT 1‑L 4945003 Microgyria (disorder) SNOMED CT 1‑L 09 Overige congenitale afwijkingen zenuwstelsel CongenitaleAfwijkingen 0‑A 9904008 Congenital anomaly of cardiovascular system (disorder) SNOMED CT Aangeboren hartafwijkingen 1‑L 61959006 Common truncus arteriosus (disorder) SNOMED CT 1‑L 204296002 Discordant ventriculoarterial connection (disorder) SNOMED CT 1‑L 86299006 Tetralogy of Fallot (disorder) SNOMED CT 1‑L 45503006 Common ventricle (disorder) SNOMED CT 1‑L 7484005 Double outlet right ventricle (disorder) SNOMED CT 1‑L 360481003 Common atrioventricular canal (disorder) SNOMED CT 1‑L 253591008 Pulmonary atresia with ventricular septal defect (disorder) SNOMED CT 1‑L 63042009 Congenital atresia of tricuspid valve (disorder) SNOMED CT 1‑L 62067003 Hypoplastic left heart syndrome (disorder) SNOMED CT 1‑L 218728005 Interrupted aortic arch (disorder) SNOMED CT 1‑L 111323005 Total anomalous pulmonary venous return (disorder) SNOMED CT 1‑L 281587000 Pentalogy of Cantrell (disorder) SNOMED CT 1‑L 7305005 Coarctation of aorta (disorder) SNOMED CT 1‑L 22 Overige congenitale afwijking hart en bloedvaten CongenitaleAfwijkingen 0‑A 95470009 Congenital anomaly of digestive tract (disorder) SNOMED CT Aangeboren afwijkingen tractus digestivus 1‑L 87979003 Cleft palate (disorder) SNOMED CT 1‑L 60983006 Congenital esophagotracheal fistula (disorder) SNOMED CT 1‑L 26179002 Congenital atresia of esophagus (disorder) SNOMED CT 1‑L 204659003 Esophageal atresia with tracheoesophageal fistula (disorder) SNOMED CT 1‑L 51118003 Congenital atresia of duodenum (disorder) SNOMED CT 1‑L 360491009 atresie van jejunum (aandoening) SNOMED CT 1‑L 25896009 atresie van ileum (aandoening) SNOMED CT 1‑L 37054000 Congenital atresia of colon (disorder) SNOMED CT 1‑L 33225004 Anorectal anomaly (disorder) SNOMED CT 1‑L 18735004 omfalocele (aandoening) SNOMED CT 1‑L 72951007 gastroschisis (aandoening) SNOMED CT 1‑L 77480004 Congenital biliary atresia (disorder) SNOMED CT 1‑L 30 Overige congenitale afwijking tractus digestivus CongenitaleAfwijkingen 0‑A 287085006 Genitourinary congenital anomalies (disorder) SNOMED CT Aangeboren afwijkingen tractus urogenitalis 1‑L 41962002 Oligohydramnios sequence (disorder) SNOMED CT 1‑S 204949001 Renal dysplasia (disorder) SNOMED CT 2‑L 28770003 Polycystic kidney disease, infantile type (disorder) SNOMED CT 2‑L 28728008 Polycystic kidney disease, adult type (disorder) SNOMED CT 1‑L 7163005 obstructieve uropathie (aandoening) SNOMED CT 1‑L 61758007 Exstrophy of bladder sequence (disorder) SNOMED CT 1‑L 69 Overige congenitale afwijking tractus urogenitalis CongenitaleAfwijkingen 0‑A 409709004 Chromosomal disorder (disorder) SNOMED CT Chromosomale afwijkingen  1‑L 21111006 Complete trisomy 13 syndrome (disorder) SNOMED CT 1‑L 51500006 syndroom van Edwards (aandoening) SNOMED CT 1‑L 41040004 Complete trisomy 21 syndrome (disorder) SNOMED CT 1‑L 74345006 Congenital disorder due to abnormality of chromosome number OR structure (disorder) SNOMED CT 1‑L 66651005 Triploidy syndrome (disorder) SNOMED CT 1‑L 400038003 Congenital malformation syndrome (disorder) SNOMED CT 0‑A 276654001 Congenital malformation (disorder SNOMED CT Andere aangeboren afwijkingen  1‑L 105986008 Congenital skeletal dysplasia (disorder) SNOMED CT 1‑L 17190001 Congenital diaphragmatic hernia (disorder) SNOMED CT 1‑L 276508000 Hydrops fetalis (disorder) SNOMED CT 1‑L 59566000 Oligohydramnios (disorder) SNOMED CT 1‑L 240104008 Congenital myotonic dystrophy (disorder) SNOMED CT 1‑L 41337007 Conjoined twins (disorder) SNOMED CT 1‑L 53189005 Congenital atresia of trachea (disorder) SNOMED CT 0‑A 275260000 Congenital malformation of the respiratory system (disorder) SNOMED CT Aangeboren afwijkingen luchtwegen 1‑L 111318005 Congenital cystic adenomatoid malformation of lung (disorder) SNOMED CT 1‑L 204508009 Choanal atresia (disorder) SNOMED CT 1‑L 38 Overige congenitale afwijking tractus respiratorius CongenitaleAfwijkingen Legenda: Type L=leaf, S=specializable, A=abstract, D=deprecated. 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