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 |
|
|
|