Waardelijst CongenitaleAfwijking22 Congenitale afwijking (2.2) 2014‑01‑24 16:38:09

Waardelijst-naam Waardelijst-id Versie / ingangsdatum Status CongenitaleAfwijking22 2.16.840.1.113883.2.4.11.196 2014‑01‑24 16:38:09 Ontwerp Bron codesysteem: 2.16.840.1.113883.6.96 Snomed 2.16.840.1.113883.2.4.4.13.8 CongenitaleAfwijkingen 2.16.840.1.113883.5.1008 NullFlavor Niveau/ Type Code Weergavenaam Codesysteem Omschrijving 0-L 88425004 Congenital anomaly of nervous system (disorder) Snomed 1-L  609417004 Fetal anencephaly (disorder) Snomed 1-L  431265009 Fetal microcephaly (disorder) Snomed 1-L  76916001 Spina bifida occulta (disorder) Snomed 1-L  414667000 Meningomyelocele (disorder) Snomed 1-L  171131006 Meningocele (disorder) Snomed 1-L  47032000 Congenital hydrocephalus (disorder) Snomed 1-L  30915001 Holoprosencephaly sequence (disorder) Snomed 1-L  55999004 Encephalocele (disorder) Snomed 1-L  363222009 Neonatal neuromuscular disorder (disorder) Snomed 1-L  09 overige congenitale afwijkingen zenuwstelsel CongenitaleAfwijkingen 0-L B zintuigen CongenitaleAfwijkingen 1-L  19416009 Congenital anomaly of eye (disorder) Snomed 2-L   61142002 Microphthalmos (disorder) Snomed 2-L   11 overige congenitale afwijkingen ogen CongenitaleAfwijkingen 1-L  8380000 Congenital anomaly of ear (disorder) Snomed 1-L  13 overige congenitale afwijkingen zintuigen CongenitaleAfwijkingen 0-L 9904008 Congenital anomaly of cardiovascular system (disorder) Snomed 1-L  204470001 Single umbilical artery (disorder) Snomed 1-L  204296002 Discordant ventriculoarterial connection (disorder) Snomed 1-L  86299006 Tetralogy of Fallot (disorder) Snomed 1-L  30288003 Ventricular septal defect (disorder) Snomed 1-L  62067003 Hypoplastic left heart syndrome (disorder) Snomed 1-L  7305005 Coarctation of aorta (disorder) Snomed 1-L  4374004 Congenital anomaly of tricuspid valve (disorder) Snomed 1-L  94702005 Multiple congenital cardiac defects (disorder) Snomed 1-L  22 overige congenitale afwijking hart en bloedvaten CongenitaleAfwijkingen 0-L 95470009 Congenital anomaly of digestive tract (disorder) Snomed 1-L  80281008 Cleft lip (disorder) Snomed 1-L  87979003 Cleft palate (disorder) Snomed 1-L  69771008 Congenital anomaly of esophagus (disorder) Snomed 1-L  84296002 Congenital atresia of small intestine (disorder) Snomed 1-L  204711007 Atresia of large intestine (disorder) Snomed 1-L  204712000 Anal atresia (disorder) Snomed 1-L  204739008 Hirschsprung's disease (disorder) Snomed 1-L  29980002 Congenital malrotation of intestine (disorder) Snomed 1-L  9707006 Intestinal volvulus (disorder) Snomed 1-L  30 overige congenitale afwijking tractus digestivus CongenitaleAfwijkingen 0-L 77868001 Congenital anomaly of respiratory system (disorder) Snomed 1-L  204508009 Choanal atresia (disorder) Snomed 1-L  14532008 Congenital anomaly of trachea (disorder) Snomed 1-L  80825009 Congenital hypoplasia of lung (disorder) Snomed 1-L  66987001 Congenital lobar emphysema (disorder) Snomed 1-L  111318005 Congenital cystic adenomatoid malformation of lung (disorder) Snomed 1-L  79231000 Hydrothorax (disorder) Snomed 1-L  83035003 Chylothorax (disorder) Snomed 1-L  17190001 Congenital diaphragmatic hernia (disorder) Snomed 1-L  21524000 Relaxation of diaphragm (disorder) Snomed 1-L  38 overige congenitale afwijking tractus respiratorius CongenitaleAfwijkingen 0-L 287085006 Genitourinary congenital anomalies (disorder) Snomed 1-L  416010008 Hypospadias (disorder) Snomed 1-L  406476007 Epispadias (disorder) Snomed 1-L  204878001 Undescended testicle (disorder) Snomed 1-L  61758007 Exstrophy of bladder sequence (disorder) Snomed 1-L  41962002 Oligohydramnios sequence (disorder) Snomed 1-L  82525005 Congenital cystic kidney disease (disorder) Snomed 1-L  7163005 Urinary tract obstruction (disorder) Snomed 1-L  39179006 Disorder of sexual differentiation (disorder) Snomed 1-L  69 overige congenitale afwijking tractus urogenitalis CongenitaleAfwijkingen 0-L 199879009 Congenital anomaly of skin (disorder) Snomed 1-L  93471006 Hemangioma of skin (disorder) Snomed 1-L  398943008 Congenital pigmented melanocytic nevus of skin (disorder) Snomed 1-L  74 overige congenitale huidafwijking CongenitaleAfwijkingen 0-L 81336004 Congenital anomaly of abdominal wall (disorder) Snomed 1-L  72951007 Gastroschisis (disorder) Snomed 1-L  18735004 Congenital omphalocele (disorder) Snomed 1-L  396347007 Umbilical hernia (disorder) Snomed 1-L  429200006 Congenital inguinal hernia (disorder) Snomed 1-L  85 overige congenitale afwijking buikwand CongenitaleAfwijkingen 0-L 73573004 Congenital anomaly of musculoskeletal system (disorder) Snomed 1-L  367506006 Polydactyly (disorder) Snomed 1-L  373413006 Syndactyly (disorder) Snomed 1-L  302297009 Congenital deformity of foot (disorder) Snomed 1-L  45806008 Reduction deformity of upper limb (disorder) Snomed 1-L  77595004 Reduction deformity of lower limb (disorder) Snomed 1-L  96 overige congenitale afwijking extremiteiten CongenitaleAfwijkingen 1-L  36172001 Congenital subluxation of hip (disorder) Snomed 1-L  98 overige congenitale afwijking skelet en spierstelsel CongenitaleAfwijkingen 0-L J multipele/syndromale congenitale afwijkingen (niet chromosomaal) CongenitaleAfwijkingen 1-L  104 overige multipele/syndromale afwijkingen CongenitaleAfwijkingen 0-L K overige congenitale afwijkingen CongenitaleAfwijkingen 1-L  276720006 Dysmorphism (disorder) Snomed 1-L  43876007 Situs inversus viscerum (disorder) Snomed 1-L  444406006 Multiple congenital anomalies (disorder) Snomed 1-L  82354003 Multiple system malformation syndrome (disorder) Snomed 1-L  217710005 Congenital iodine deficiency syndrome (disorder) Snomed 1-L  86095007 Inborn error of metabolism (disorder) Snomed 1-L  112 andere endocrinologische afwijkingen CongenitaleAfwijkingen 1-L  363346000:246454002=255399007 Congenital malignant neoplastic disease (disorder) Snomed   OTH overig NullFlavor   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. CSV XML