| Niveau/ Type |
Code |
Weergavenaam |
Codesysteem |
| 0‑L |
88425004
|
Congenital anomaly of nervous system (disorder)
|
SNOMED CT |
| 1‑L |
609417004
|
Fetal anencephaly (disorder)
|
SNOMED CT |
| 1‑L |
431265009
|
Fetal microcephaly (disorder)
|
SNOMED CT |
| 1‑L |
76916001
|
Spina bifida occulta (disorder)
|
SNOMED CT |
| 1‑L |
414667000
|
Meningomyelocele (disorder)
|
SNOMED CT |
| 1‑L |
171131006
|
Meningocele (disorder)
|
SNOMED CT |
| 1‑L |
47032000
|
Congenital hydrocephalus (disorder)
|
SNOMED CT |
| 1‑L |
30915001
|
Holoprosencephaly sequence (disorder)
|
SNOMED CT |
| 1‑L |
55999004
|
Encephalocele (disorder)
|
SNOMED CT |
| 1‑L |
363222009
|
Neonatal neuromuscular disorder (disorder)
|
SNOMED CT |
| 1‑L |
09
|
overige congenitale afwijkingen zenuwstelsel
|
CongenitaleAfwijkingen |
| 0‑L |
B
|
zintuigen
|
CongenitaleAfwijkingen |
| 1‑L |
19416009
|
Congenital anomaly of eye (disorder)
|
SNOMED CT |
| 2‑L |
61142002
|
Microphthalmos (disorder)
|
SNOMED CT |
| 2‑L |
11
|
overige congenitale afwijkingen ogen
|
CongenitaleAfwijkingen |
| 1‑L |
8380000
|
Congenital anomaly of ear (disorder)
|
SNOMED CT |
| 1‑L |
13
|
overige congenitale afwijkingen zintuigen
|
CongenitaleAfwijkingen |
| 0‑L |
9904008
|
Congenital anomaly of cardiovascular system (disorder)
|
SNOMED CT |
| 1‑L |
204470001
|
Single umbilical artery (disorder)
|
SNOMED CT |
| 1‑L |
204296002
|
Discordant ventriculoarterial connection (disorder)
|
SNOMED CT |
| 1‑L |
86299006
|
Tetralogy of Fallot (disorder)
|
SNOMED CT |
| 1‑L |
30288003
|
Ventricular septal defect (disorder)
|
SNOMED CT |
| 1‑L |
62067003
|
Hypoplastic left heart syndrome (disorder)
|
SNOMED CT |
| 1‑L |
7305005
|
Coarctation of aorta (disorder)
|
SNOMED CT |
| 1‑L |
4374004
|
Congenital anomaly of tricuspid valve (disorder)
|
SNOMED CT |
| 1‑L |
94702005
|
Multiple congenital cardiac defects (disorder)
|
SNOMED CT |
| 1‑L |
22
|
overige congenitale afwijking hart en bloedvaten
|
CongenitaleAfwijkingen |
| 0‑L |
95470009
|
Congenital anomaly of digestive tract (disorder)
|
SNOMED CT |
| 1‑L |
80281008
|
Cleft lip (disorder)
|
SNOMED CT |
| 1‑L |
87979003
|
Cleft palate (disorder)
|
SNOMED CT |
| 1‑L |
69771008
|
Congenital anomaly of esophagus (disorder)
|
SNOMED CT |
| 1‑L |
84296002
|
Congenital atresia of small intestine (disorder)
|
SNOMED CT |
| 1‑L |
204711007
|
Atresia of large intestine (disorder)
|
SNOMED CT |
| 1‑L |
204712000
|
Anal atresia (disorder)
|
SNOMED CT |
| 1‑L |
204739008
|
Hirschsprung's disease (disorder)
|
SNOMED CT |
| 1‑L |
29980002
|
Congenital malrotation of intestine (disorder)
|
SNOMED CT |
| 1‑L |
9707006
|
Intestinal volvulus (disorder)
|
SNOMED CT |
| 1‑L |
30
|
overige congenitale afwijking tractus digestivus
|
CongenitaleAfwijkingen |
| 0‑L |
77868001
|
Congenital anomaly of respiratory system (disorder)
|
SNOMED CT |
| 1‑L |
204508009
|
Choanal atresia (disorder)
|
SNOMED CT |
| 1‑L |
14532008
|
Congenital anomaly of trachea (disorder)
|
SNOMED CT |
| 1‑L |
80825009
|
Congenital hypoplasia of lung (disorder)
|
SNOMED CT |
| 1‑L |
66987001
|
Congenital lobar emphysema (disorder)
|
SNOMED CT |
| 1‑L |
111318005
|
Congenital cystic adenomatoid malformation of lung (disorder)
|
SNOMED CT |
| 1‑L |
79231000
|
Hydrothorax (disorder)
|
SNOMED CT |
| 1‑L |
83035003
|
Chylothorax (disorder)
|
SNOMED CT |
| 1‑L |
17190001
|
Congenital diaphragmatic hernia (disorder)
|
SNOMED CT |
| 1‑L |
21524000
|
Relaxation of diaphragm (disorder)
|
SNOMED CT |
| 1‑L |
38
|
overige congenitale afwijking tractus respiratorius
|
CongenitaleAfwijkingen |
| 0‑L |
287085006
|
Genitourinary congenital anomalies (disorder)
|
SNOMED CT |
| 1‑L |
416010008
|
Hypospadias (disorder)
|
SNOMED CT |
| 1‑L |
406476007
|
Epispadias (disorder)
|
SNOMED CT |
| 1‑L |
204878001
|
Undescended testicle (disorder)
|
SNOMED CT |
| 1‑L |
61758007
|
Exstrophy of bladder sequence (disorder)
|
SNOMED CT |
| 1‑L |
41962002
|
Oligohydramnios sequence (disorder)
|
SNOMED CT |
| 1‑L |
82525005
|
Congenital cystic kidney disease (disorder)
|
SNOMED CT |
| 1‑L |
7163005
|
Urinary tract obstruction (disorder)
|
SNOMED CT |
| 1‑L |
39179006
|
Disorder of sexual differentiation (disorder)
|
SNOMED CT |
| 1‑L |
69
|
overige congenitale afwijking tractus urogenitalis
|
CongenitaleAfwijkingen |
| 0‑L |
199879009
|
Congenital anomaly of skin (disorder)
|
SNOMED CT |
| 1‑L |
93471006
|
Hemangioma of skin (disorder)
|
SNOMED CT |
| 1‑L |
398943008
|
Congenital pigmented melanocytic nevus of skin (disorder)
|
SNOMED CT |
| 1‑L |
74
|
overige congenitale huidafwijking
|
CongenitaleAfwijkingen |
| 0‑L |
81336004
|
Congenital anomaly of abdominal wall (disorder)
|
SNOMED CT |
| 1‑L |
72951007
|
Gastroschisis (disorder)
|
SNOMED CT |
| 1‑L |
18735004
|
Congenital omphalocele (disorder)
|
SNOMED CT |
| 1‑L |
396347007
|
Umbilical hernia (disorder)
|
SNOMED CT |
| 1‑L |
429200006
|
Congenital inguinal hernia (disorder)
|
SNOMED CT |
| 1‑L |
85
|
overige congenitale afwijking buikwand
|
CongenitaleAfwijkingen |
| 0‑L |
73573004
|
Congenital anomaly of musculoskeletal system (disorder)
|
SNOMED CT |
| 1‑L |
367506006
|
Polydactyly (disorder)
|
SNOMED CT |
| 1‑L |
373413006
|
Syndactyly (disorder)
|
SNOMED CT |
| 1‑L |
302297009
|
Congenital deformity of foot (disorder)
|
SNOMED CT |
| 1‑L |
45806008
|
Reduction deformity of upper limb (disorder)
|
SNOMED CT |
| 1‑L |
77595004
|
Reduction deformity of lower limb (disorder)
|
SNOMED CT |
| 1‑L |
96
|
overige congenitale afwijking extremiteiten
|
CongenitaleAfwijkingen |
| 1‑L |
36172001
|
Congenital subluxation of hip (disorder)
|
SNOMED CT |
| 1‑L |
98
|
overige congenitale afwijking skelet en spierstelsel
|
CongenitaleAfwijkingen |
| 0‑L |
J
|
multipele/syndromale congenitale afwijkingen (niet chromosomaal)
|
CongenitaleAfwijkingen |
| 1‑L |
276720006
|
Dysmorphism (disorder)
|
SNOMED CT |
| 1‑L |
43876007
|
Situs inversus viscerum (disorder)
|
SNOMED CT |
| 1‑L |
444406006
|
Multiple congenital anomalies (disorder)
|
SNOMED CT |
| 1‑L |
82354003
|
Multiple system malformation syndrome (disorder)
|
SNOMED CT |
| 1‑L |
104
|
overige multipele/syndromale afwijkingen
|
CongenitaleAfwijkingen |
| 0‑L |
K
|
overige congenitale afwijkingen
|
CongenitaleAfwijkingen |
| 1‑L |
217710005
|
Congenital iodine deficiency syndrome (disorder)
|
SNOMED CT |
| 1‑L |
86095007
|
Inborn error of metabolism (disorder)
|
SNOMED CT |
| 1‑L |
112
|
andere endocrinologische afwijkingen
|
CongenitaleAfwijkingen |
| 1‑L |
363346000:246454002=255399007
|
Congenital malignant neoplastic disease (disorder)
|
SNOMED CT |
|
| 0‑L |
OTH
|
overig
|
NullFlavor |
| 0‑L |
NI
|
geen informatie
|
NullFlavor |
Waardelijst Congenitale afwijking (2.2) 2014‑01‑24 16:38:09
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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.