| Niveau/ Type |
Code |
Weergavenaam |
Codesysteem |
| 0‑S |
88425004
|
congenitale misvorming van zenuwstelsel (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
1829003
|
microcefalie (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
76916001
|
spina bifida occulta (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
414667000
|
meningomyelocele (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
171131006
|
meningocele (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
55999004
|
encephalocele (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
30023002
|
hydranencefalie (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
47032000
|
congenitale hydrocefalus (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
30915001
|
holoprosencefalie (aandoening)
|
SNOMED Clinical Terms |
| 0‑S |
9904008
|
congenitale afwijking van tractus circulatorius (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
204470001
|
enkele navelstrengarterie (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
30288003
|
ventrikelseptumdefect (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
204296002
|
discordante ventriculoarteriële verbinding (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
86299006
|
tetralogie van Fallot (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
62067003
|
hypoplastisch-linkerhartsyndroom (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
7305005
|
aortacoarctatie (aandoening)
|
SNOMED Clinical Terms |
| 0‑S |
95470009
|
congenitale afwijking van tractus digestivus (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
449790007
|
cheilognathopalatoschisis (aandoening)
|
SNOMED Clinical Terms |
| 2‑L |
87979003
|
palatoschisis (aandoening)
|
SNOMED Clinical Terms |
| 2‑L |
80281008
|
cheiloschisis (aandoening)
|
SNOMED Clinical Terms |
| 0‑L |
204712000
|
congenitale atresie van anus (aandoening)
|
SNOMED Clinical Terms |
| 0‑L |
18735004
|
omfalocele (aandoening)
|
SNOMED Clinical Terms |
| 0‑L |
72951007
|
gastroschisis (aandoening)
|
SNOMED Clinical Terms |
| 0‑S |
287085006
|
congenitale afwijking van tractus urogenitalis (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
41962002
|
syndroom van Potter (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
82525005
|
congenitale polycysteuze nierziekte (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
7163005
|
obstructie van urinewegen (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
61758007
|
exstrofie van blaas (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
416010008
|
hypospadie (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
406476007
|
epispadie (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
204878001
|
niet-ingedaalde testis (aandoening)
|
SNOMED Clinical Terms |
| 1‑L |
39179006
|
stoornis in geslachtelijke ontwikkeling (aandoening)
|
SNOMED Clinical Terms |
| 0‑S |
74345006
|
congenitale aandoening door chromosoomafwijking (aandoening)
|
SNOMED Clinical Terms |
|
Waardelijst ProbleemNaam_Congenitale Afwijking Obstetrie 2021‑05‑20 16:15:36
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