| Niveau/ Type |
Code |
Weergavenaam |
Codesysteem |
| 0‑L |
276508000
|
hydrops foetalis (aandoening)
|
SNOMED |
| 0‑L |
88425004
|
congenitale misvorming van zenuwstelsel (aandoening)
|
SNOMED |
| 1‑L |
609417004
|
foetale anencefalie (aandoening)
|
SNOMED |
| 1‑L |
431265009
|
microcefalie bij foetus (aandoening)
|
SNOMED |
| 1‑L |
76916001
|
spina bifida occulta (aandoening)
|
SNOMED |
| 1‑L |
414667000
|
meningomyelocele (aandoening)
|
SNOMED |
| 1‑L |
171131006
|
meningocele (aandoening)
|
SNOMED |
| 1‑L |
47032000
|
congenitale hydrocefalus (aandoening)
|
SNOMED |
| 1‑L |
30915001
|
holoprosencefalie (aandoening)
|
SNOMED |
| 1‑L |
55999004
|
encephalocele (aandoening)
|
SNOMED |
| 1‑L |
363222009
|
neonatale neuromusculaire aandoening (aandoening)
|
SNOMED |
| 1‑L |
09
|
Overige congenitale afwijkingen zenuwstelsel
|
CongenitaleAfwijkingen |
| 0‑L |
B
|
Zintuigen
|
CongenitaleAfwijkingen |
| 1‑L |
19416009
|
congenitale afwijking van oog (aandoening)
|
SNOMED |
| 2‑L |
61142002
|
microftalmie (aandoening)
|
SNOMED |
| 2‑L |
11
|
Overige congenitale afwijkingen ogen
|
CongenitaleAfwijkingen |
| 1‑D |
8380000
|
Congenital anomaly of ear (disorder)
|
SNOMED |
| 1‑L |
275259005
|
congenitale malformatie van oor (aandoening)
|
SNOMED |
| 1‑L |
13
|
Overige congenitale afwijkingen zintuigen
|
CongenitaleAfwijkingen |
| 0‑L |
9904008
|
congenitale afwijking van tractus circulatorius (aandoening)
|
SNOMED |
| 1‑L |
204470001
|
enkele navelstrengarterie (aandoening)
|
SNOMED |
| 1‑L |
204296002
|
discordante ventriculoarteriële verbinding (aandoening)
|
SNOMED |
| 1‑L |
86299006
|
tetralogie van Fallot (aandoening)
|
SNOMED |
| 1‑L |
30288003
|
ventrikelseptumdefect (aandoening)
|
SNOMED |
| 1‑L |
62067003
|
hypoplastisch-linkerhartsyndroom (aandoening)
|
SNOMED |
| 1‑L |
7305005
|
aortacoarctatie (aandoening)
|
SNOMED |
| 1‑L |
4374004
|
congenitale misvorming van tricuspidalisklep (aandoening)
|
SNOMED |
| 1‑L |
94702005
|
multipele congenitale hartdefecten (aandoening)
|
SNOMED |
| 1‑L |
22
|
Overige congenitale afwijking hart en bloedvaten
|
CongenitaleAfwijkingen |
| 0‑L |
95470009
|
congenitale afwijking van tractus digestivus (aandoening)
|
SNOMED |
| 1‑L |
80281008
|
cheiloschisis (aandoening)
|
SNOMED |
| 1‑L |
87979003
|
palatoschisis (aandoening)
|
SNOMED |
| 1‑L |
69771008
|
congenitale misvorming van oesofagus (aandoening)
|
SNOMED |
| 1‑L |
84296002
|
congenitale atresie van dunne darm (aandoening)
|
SNOMED |
| 1‑L |
204711007
|
atresie van dikke darm (aandoening)
|
SNOMED |
| 1‑L |
204712000
|
congenitale atresie van anus (aandoening)
|
SNOMED |
| 1‑L |
204739008
|
ziekte van Hirschsprung (aandoening)
|
SNOMED |
| 1‑L |
29980002
|
congenitale malrotatie van darm (aandoening)
|
SNOMED |
| 1‑L |
9707006
|
intestinale volvulus (aandoening)
|
SNOMED |
| 1‑L |
30
|
Overige congenitale afwijking tractus digestivus
|
CongenitaleAfwijkingen |
| 0‑L |
77868001
|
Congenital anomaly of respiratory system (disorder)
|
SNOMED |
| 1‑L |
204508009
|
choanale atresie (aandoening)
|
SNOMED |
| 1‑L |
14532008
|
congenitale malformatie van trachea (aandoening)
|
SNOMED |
| 1‑L |
80825009
|
congenitale hypoplasie van long (aandoening)
|
SNOMED |
| 1‑L |
66987001
|
congenitaal lobair emfyseem (aandoening)
|
SNOMED |
| 1‑L |
111318005
|
congenitale cysteuze adenomatoïde malformatie van long (aandoening)
|
SNOMED |
| 1‑L |
79231000
|
hydrothorax (aandoening)
|
SNOMED |
| 1‑L |
83035003
|
chylothorax (aandoening)
|
SNOMED |
| 1‑L |
17190001
|
congenitale hernia diaphragmatica (aandoening)
|
SNOMED |
| 1‑L |
21524000
|
relaxatie van diafragma (aandoening)
|
SNOMED |
| 1‑L |
38
|
Overige congenitale afwijking tractus respiratorius
|
CongenitaleAfwijkingen |
| 0‑L |
287085006
|
congenitale afwijking van tractus urogenitalis (aandoening)
|
SNOMED |
| 1‑L |
416010008
|
hypospadie (aandoening)
|
SNOMED |
| 1‑L |
406476007
|
epispadie (aandoening)
|
SNOMED |
| 1‑L |
204878001
|
niet-ingedaalde testis (aandoening)
|
SNOMED |
| 1‑L |
61758007
|
exstrofie van blaas (aandoening)
|
SNOMED |
| 1‑L |
41962002
|
syndroom van Potter (aandoening)
|
SNOMED |
| 1‑L |
82525005
|
congenitale polycysteuze nierziekte (aandoening)
|
SNOMED |
| 1‑L |
7163005
|
obstructie van urinewegen (aandoening)
|
SNOMED |
| 1‑L |
39179006
|
stoornis in geslachtelijke ontwikkeling (aandoening)
|
SNOMED |
| 1‑L |
69
|
Overige congenitale afwijking tractus urogenitalis
|
CongenitaleAfwijkingen |
| 0‑L |
199879009
|
congenitale misvorming van huid (aandoening)
|
SNOMED |
| 1‑L |
93471006
|
hemangioom van huid (aandoening)
|
SNOMED |
| 1‑L |
398943008
|
naevus naevocellularis van huid (aandoening)
|
SNOMED |
| 1‑L |
74
|
Overige congenitale huidafwijking
|
CongenitaleAfwijkingen |
| 0‑L |
81336004
|
congenitale afwijking van buikwand (aandoening)
|
SNOMED |
| 1‑L |
72951007
|
gastroschisis (aandoening)
|
SNOMED |
| 1‑L |
18735004
|
omfalocele (aandoening)
|
SNOMED |
| 1‑L |
396347007
|
hernia umbilicalis (aandoening)
|
SNOMED |
| 1‑L |
429200006
|
congenitale hernia inguinalis (aandoening)
|
SNOMED |
| 1‑L |
85
|
Overige congenitale afwijking buikwand
|
CongenitaleAfwijkingen |
| 0‑L |
73573004
|
congenitale afwijking van bewegingsstelsel (aandoening)
|
SNOMED |
| 1‑L |
367506006
|
polydactylie (aandoening)
|
SNOMED |
| 1‑L |
373413006
|
syndactylie (aandoening)
|
SNOMED |
| 1‑L |
302297009
|
congenitale deformiteit van voet (aandoening)
|
SNOMED |
| 1‑L |
45806008
|
reductiedefect van bovenste extremiteit (aandoening)
|
SNOMED |
| 1‑L |
77595004
|
congenitaal lengtedefect van gehele onderste extremiteit (aandoening)
|
SNOMED |
| 1‑L |
96
|
Overige congenitale afwijking extremiteiten
|
CongenitaleAfwijkingen |
| 1‑L |
36172001
|
congenitale subluxatie van heup (aandoening)
|
SNOMED |
| 1‑L |
98
|
Overige congenitale afwijking skelet en spierstelsel
|
CongenitaleAfwijkingen |
| 0‑L |
J
|
Multipele/syndromale congenitale afwijkingen (niet chromosomaal)
|
CongenitaleAfwijkingen |
| 1‑L |
276720006
|
dysmorfie (aandoening)
|
SNOMED |
| 1‑L |
43876007
|
situs inversus viscerum (aandoening)
|
SNOMED |
| 1‑L |
444406006
|
Multiple congenital anomalies (disorder)
|
SNOMED |
| 1‑L |
82354003
|
malformatiesyndroom met betrokkenheid van meerdere systemen (aandoening)
|
SNOMED |
| 1‑L |
104
|
Overige multipele/syndromale afwijkingen
|
CongenitaleAfwijkingen |
| 0‑L |
K
|
Overige congenitale afwijkingen
|
CongenitaleAfwijkingen |
| 1‑L |
217710005
|
congenitale-jodiumdeficiëntiesyndroom (aandoening)
|
SNOMED |
| 1‑L |
112
|
Andere endocrinologische afwijkingen
|
CongenitaleAfwijkingen |
| 1‑L |
86095007
|
aangeboren defect van stofwisseling (aandoening)
|
SNOMED |
| 1‑L |
363346000:246454002=255399007
|
Congenital malignant neoplastic disease (disorder)
|
SNOMED |
|
| 0‑L |
OTH
|
Overig
|
NullFlavor |
| 0‑L |
NI
|
Geen informatie
|
NullFlavor |
Waardelijst Congenitale afwijking 2021‑03‑23 15:38:25
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of the International Health Terminology Standards Development Organisation (IHTSDO).
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- for more information contact http://www.snomed.org/snomed-ct/getsnomed-ct or info@snomed.org.