Waardelijst CongenitaleAfwijking22

Waardelijst Congenitale afwijking (2.2) 2014‑01‑24 16:38:09

2.16.840.1.113883.2.4.11.196

Geldigheid

geldig vanaf 2014‑01‑24 16:38:09

Andere versies van deze waardelijst

Congenitale afwijking 2.3 - 2016‑11‑10 14:40:18

Status

Definitief

Versielabel

2.2

Naam

CongenitaleAfwijking22

Weergavenaam

Congenitale afwijking (2.2)

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

2.16.840.1.113883.2.4.4.13.8 - CongenitaleAfwijkingen

2.16.840.1.113883.5.1008 - NullFlavor

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

Legenda: Type L=leaf, S=specializable, A=abstract, D=deprecated. NullFlavors komen in het attribuut @nullFlavor in plaats van in @code.

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Waardelijst Congenitale afwijking (2.2) 2014‑01‑24 16:38:09