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final Waardelijst Congenitale afwijking 2019‑10‑10 09:12:29

Id 2.16.840.1.113883.2.4.11.196 Ingangsdatum 2019‑10‑10 09:12:29
Status final Definitief Versielabel 2.3
Naam CongenitaleAfwijking22 Weergavenaam Congenitale afwijking
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
2.16.840.1.113883.5.1008 - NullFlavor - http://terminology.hl7.org/CodeSystem/v3-NullFlavor
Niveau/ Type Code Weergavenaam Codesysteem
0‑L
276508000
Hydrops foetalis
SNOMED CT
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‑D
8380000
Congenital anomaly of ear (disorder)
SNOMED CT
1‑L
275259005
Congenital malformation 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
112
Andere endocrinologische afwijkingen
CongenitaleAfwijkingen
1‑L
86095007
Inborn error of metabolism (disorder)
SNOMED CT
1‑L
363346000:246454002=255399007
Congenital malignant neoplastic disease (disorder)
SNOMED CT

0‑L
OTH
Overig
NullFlavor
0‑L
NI
Geen informatie
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