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draft Waardelijst KraamKindProbleemNaamCodelijst 2019‑03‑12 14:52:13

Id 2.16.840.1.113883.2.4.11.257 Ingangsdatum 2019‑03‑12 14:52:13
Status draft Ontwerp Versielabel
Naam KraamKindProbleemNaamCodelijst Weergavenaam KraamKindProbleemNaamCodelijst
Copyright en-US 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.
3 bron codesystemen
2.16.840.1.113883.6.96 - SNOMED CT - http://snomed.info/sct
2.16.840.1.113883.2.4.4.13.8 - CongenitaleAfwijkingen - urn:oid:2.16.840.1.113883.2.4.4.13.8
2.16.840.1.113883.2.4.3.22.1.2.64 - KADiagnose - urn:oid:2.16.840.1.113883.2.4.3.22.1.2.64
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
0‑L
276519002
Neonatal hypotension (disorder)
SNOMED CT
0‑L
83330001
Patent ductus arteriosus (disorder)
SNOMED CT
0‑L
698247007
Cardiac arrhythmia (disorder)
SNOMED CT
0‑L
9904008
Congenital anomaly of cardiovascular system (disorder)
SNOMED CT
0‑L
195506001
Idiopathic hypotension (disorder)
SNOMED CT
0‑L
234171009
Drug-induced hypotension (disorder)
SNOMED CT
0‑L
45007003
Low blood pressure (disorder)
SNOMED CT
0‑L
72654001
Supraventricular arrhythmia (disorder)
SNOMED CT
0‑L
56110009
Birth trauma of fetus (disorder)
SNOMED CT
1‑L
126941005
Subdural intracranial hemorrhage due to birth trauma (disorder)
SNOMED CT
1‑L
206399009
Intracranial subarachnoid hemorrhage due to birth injury (disorder)
SNOMED CT
1‑L
206192007
Tentorial tear due to birth trauma (disorder)
SNOMED CT
1‑L
219
Overige bloedingen (geboortetrauma)
KADiagnose
1‑L
371129000
Paralysis from birth trauma (disorder)
SNOMED CT
1‑L
290
Overige geboortetraumata
KADiagnose
0‑L
82353009
Congenital infectious disease (disorder)
SNOMED CT
1‑L
35742006
Congenital syphilis (disorder)
SNOMED CT
1‑L
73893000
Congenital toxoplasmosis (disorder)
SNOMED CT
1‑L
59527008
Congenital cytomegalovirus infection (disorder)
SNOMED CT
1‑L
1857005
Congenital rubella syndrome (disorder)
SNOMED CT
1‑L
206376005
Sepsis of the newborn (disorder)
SNOMED CT
1‑L
39367000
Inflammatory disease of the central nervous system (disorder)
SNOMED CT
1‑L
1450
Overige infecties
KADiagnose
0‑L
406
Immunologische en haematologische stoornissen
KADiagnose
1‑L
414030009
Disorder of immune structure (disorder)
SNOMED CT
1‑L
414028007
Disorder of hematopoietic system in newborn (disorder)
SNOMED CT
2‑L
13404009
Twin-to-twin blood transfer (disorder)
SNOMED CT
2‑L
3580
Overig haematologisch
KADiagnose
0‑L
267574006
Nervous system and sense organ diseases (disorder)
SNOMED CT
1‑L
276647007
Perinatal intracranial hemorrhage (disorder)
SNOMED CT
1‑L
206576006
Neonatal cerebral ischemia (disorder)
SNOMED CT
1‑L
87476004
Convulsions in the newborn (disorder)
SNOMED CT
1‑L
205294008
Neonatal hypotonia (disorder)
SNOMED CT
1‑L
415297005
Retinopathy of prematurity (disorder)
SNOMED CT
1‑L
95827002
Congenital hearing disorder (disorder)
SNOMED CT
0‑L
363696006
Neonatal cardiovascular disorder (disorder)
SNOMED CT
1‑L
206596003
Neonatal hypertension (disorder)
SNOMED CT
1‑L
276519002
Neonatal hypotension (disorder)
SNOMED CT
1‑L
276508000
Hydrops fetalis (disorder)
SNOMED CT
1‑L
5800
Overige circulatoire problemen
KADiagnose
0‑L
363225006
Neonatal respiratory system disorder (disorder)
SNOMED CT
1‑L
46775006
Respiratory distress syndrome in the newborn (disorder)
SNOMED CT
1‑L
276533002
Neonatal aspiration syndromes (disorder)
SNOMED CT
1‑L
67569000
Bronchopulmonary dysplasia of newborn (disorder)
SNOMED CT
1‑L
6990
Overige respiratoire problemen
KADiagnose
0‑L
7100
Stoornissen tractus digestivus en navel
KADiagnose
1‑L
281610001
Neonatal hyperbilirubinemia (disorder)
SNOMED CT
1‑L
7700
Overige stoornissen tractus digestivus en navel
KADiagnose
0‑L
363221002
Neonatal metabolic and endocrinologic disorder (disorder)
SNOMED CT
1‑L
52767006
Neonatal hypoglycemia (disorder)
SNOMED CT
1‑L
276557002
Neonatal hyperglycemia (disorder)
SNOMED CT
1‑L
190268003
Congenital hypothyroidism (disorder)
SNOMED CT
1‑L
8490
Overige endocriene, metabole en milieu interieur stoornissen
KADiagnose
1‑L
363224005
Neonatal renal disorder (disorder)
SNOMED CT

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