learning_disability
Codelist metadata
-
Coding system
- SNOMED CT
-
Coding system release
- unknown
-
Organisation
- QCovid
-
Codelist ID
- qcovid/learning_disability
-
Version ID
- 538903d3
Versions
About
Description
SNOMED codelist for the learning_disability group in the QCovid® to develop the
COVID-19 Population Risk Assessment.
Codelist also contains the following unrecognised codes:
- 1089731000000100 | Profound intellectual development disorder with impairment of behaviour (disorder) |
- 1089741000000100 | Severe intellectual development disorder without significant impairment of behaviour (disorder) |
- 1089831000000100 | Mild intellectual development disorder without significant impairment of behaviour (disorder) |
- 1093991000000100 | Mild intellectual development disorder with impairment of behaviour (disorder) |
- 1094021000000100 | Intellectual development disorder with minimal impairment of behaviour (disorder) |
References
Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.
We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.
| code | term |
|---|---|
| 1287007 | Congenital absence of bile duct (disorder) |
| 2593002 | Dubowitz's syndrome (disorder) |
| 2829000 | Uhl's disease (disorder) |
| 4223005 | Parkinsonism caused by drug (disorder) |
| 4374004 | Congenital anomaly of tricuspid valve (disorder) |
| 4434006 | Bloom syndrome (disorder) |
| 5230009 | Congenital absence of coronary artery (disorder) |
| 5619004 | Bardet-Biedl syndrome (disorder) |
| 6996004 | Congenital absence of pulmonary valve (disorder) |
| 7305005 | Coarctation of aorta (disorder) |
| 7368005 | Double outlet left ventricle (disorder) |
| 7438000 | Congenital atresia of aorta (disorder) |
| 7484005 | Double outlet right ventricle (disorder) |
| 10007009 | Coffin-Siris syndrome (disorder) |
| 10451007 | Double aortic arch (disorder) |
| 10818008 | Congenital malposition of heart (disorder) |
| 11614003 | Congenital stenosis of pulmonary veins (disorder) |
| 12075007 | Congenital hypoplasia of ascending aorta (disorder) |
| 12770006 | Cyanotic congenital heart disease (disorder) |
| 13213009 | Congenital heart disease (disorder) |
| 13689005 | Congenital anomaly of aortic valve (disorder) |
| 13867009 | Preductal coarctation of aorta (disorder) |
| 14886009 | Abdominal heart (disorder) |
| 15096009 | Congenital insufficiency of pulmonary valve (disorder) |
| 15182000 | Coffin-Lowry syndrome (disorder) |
| 15459006 | Endocardial cushion defect (disorder) |
| 16567006 | Mesocardia (disorder) |
| 16972009 | Congenital aneurysm of aorta (disorder) |
| 17024001 | Aortopulmonary window (disorder) |
| 17122004 | 4p partial monosomy syndrome (disorder) |
| 17718000 | Ostium primum defect (disorder) |
| 19092004 | Holt-Oram syndrome (disorder) |
| 19249002 | Premature closure of foramen ovale (disorder) |
| 19972008 | Postencephalitic parkinsonism (disorder) |
| 21111006 | Complete trisomy 13 syndrome (disorder) |
| 21634003 | Borjeson-Forssman-Lehmann syndrome (disorder) |
| 21981000 | Single coronary artery (disorder) |
| 23063005 | Congenital atresia of mitral valve (disorder) |
| 23560001 | Asperger's disorder (disorder) |
| 26146002 | Complete transposition of great vessels (disorder) |
| 26201005 | Aortic left ventricular tunnel (disorder) |
| 26780008 | Coarctation of pulmonary artery (disorder) |
| 27637000 | Dextrocardia (disorder) |
| 28574005 | Congenital anomaly of coronary artery (disorder) |
| 28656008 | Congenital insufficiency of aortic valve (disorder) |
| 28975000 | Constitutional aplastic anemia (disorder) |
| 29928006 | Congenital insufficiency of mitral valve (disorder) |
| 31216003 | Profound intellectual disability (disorder) |
| 35919005 | Pervasive developmental disorder (disorder) |
| 36110001 | Congenital anomaly of pulmonary artery (disorder) |
| 36233006 | Congenital stenosis of tricuspid valve (disorder) |
| 36422005 | Transposition of pulmonary veins (disorder) |
| 36752001 | Congenital splenomegaly (disorder) |
| 37104009 | Congenital enlargement of coronary sinus (disorder) |
| 37687000 | Congenital absence of cervix (disorder) |
| 38385001 | Persistent left posterior cardinal vein (disorder) |
| 39905002 | Scimitar syndrome (disorder) |
| 40272001 | Congenital absence of coronary sinus (disorder) |
| 40354009 | De Lange syndrome (disorder) |
| 40700009 | Severe intellectual disability (disorder) |
| 41040004 | Complete trisomy 21 syndrome (disorder) |
| 41893002 | Left ventricular-right atrial communication (disorder) |
| 42402006 | Kartagener syndrome (disorder) |
| 43614003 | Autistic disorder of childhood onset (disorder) |
| 45237002 | Congenital dilatation of aorta (disorder) |
| 45259000 | Celiac infantilism (disorder) |
| 45492009 | Congenital stenosis of superior vena cava (disorder) |
| 45503006 | Common ventricle (disorder) |
| 48121000 | Congenital cardiomegaly (disorder) |
| 48520006 | Congenital atresia of cardiac vein (disorder) |
| 48796009 | Congenital nephrotic syndrome (disorder) |
| 49049000 | Parkinson's disease (disorder) |
| 50992006 | 22q partial trisomy syndrome (disorder) |
| 51442005 | Congenital atresia of aortic valve (disorder) |
| 51500006 | Complete trisomy 18 syndrome (disorder) |
| 51789008 | Congenital malposition of cardiac apex (disorder) |
| 54160000 | Congenital aneurysm of sinus of Valsalva (disorder) |
| 54682008 | Congenital hypoplasia of pulmonary artery (disorder) |
| 55510008 | Cor triatriatum (disorder) |
| 56118002 | Congenital syphilitic splenomegaly (disorder) |
| 56604005 | Cohen syndrome (disorder) |
| 58756001 | Huntington's chorea (disorder) |
| 58795000 | Distal muscular dystrophy (disorder) |
| 59631007 | Anomalous pulmonary venous drainage (disorder) |
| 59877000 | Congenital anomaly of aorta (disorder) |
| 60106004 | Common arterial trunk and separate origin of pulmonary arteries (disorder) |
| 60787001 | Congenital hypoplasia of aortic arch (disorder) |
| 61152003 | Moderate intellectual disability (disorder) |
| 61959006 | Common truncus arteriosus (disorder) |
| 62067003 | Hypoplastic left heart syndrome (disorder) |
| 62239001 | Parkinson-dementia complex of Guam (disorder) |
| 63042009 | Congenital atresia of tricuspid valve (disorder) |
| 63934006 | Overriding aorta (disorder) |
| 66403007 | Vascular ring of aorta (disorder) |
| 66758006 | Acrodysostosis (disorder) |
| 67747009 | Ocular muscular dystrophy (disorder) |
| 68092007 | Anomalous origin of pulmonary artery (disorder) |
| 68237008 | Partial anomalous pulmonary venous connection (disorder) |
| 68504005 | Ataxia-telangiectasia syndrome (disorder) |
| 68618008 | Rett's disorder (disorder) |
| 70173007 | 5p partial monosomy syndrome (disorder) |
| 70195006 | Congenital anomaly of superior vena cava (disorder) |
| 70320004 | Congenital anomaly of heart valve (disorder) |
| 70602002 | Pseudocoarctation of aorta (disorder) |
| 71961003 | Childhood disintegrative disorder (disorder) |
| 72242008 | Postductal coarctation of aorta (disorder) |
| 72352009 | Bicuspid aortic valve (disorder) |
| 73297009 | Muscular dystrophy (disorder) |
| 73699003 | Common arterial trunk and common origin of pulmonary arteries (disorder) |
| 74034002 | Isolated dextrocardia (disorder) |
| 74218008 | Coronary artery arising from main pulmonary artery (disorder) |
| 74561007 | Kommerell's diverticulum (disorder) |
| 75065003 | Endemic cretinism (disorder) |
| 75072002 | Nemaline myopathy (disorder) |
| 75270000 | Congenital diverticulum of left ventricle (disorder) |
| 75372006 | Congenital anomaly of mitral valve (disorder) |
| 75398000 | Anomalous origin of coronary artery (disorder) |
| 76670001 | Duchenne muscular dystrophy (disorder) |
| 76880004 | Angelman syndrome (disorder) |
| 77097004 | Oculopharyngeal muscular dystrophy (disorder) |
| 77480004 | Congenital biliary atresia (disorder) |
| 77593006 | Congenital bronchiectasis (disorder) |
| 77956009 | Steinert myotonic dystrophy syndrome (disorder) |
| 77978002 | Persistent left superior vena cava (disorder) |
| 78250005 | Ectopia cordis (disorder) |
| 78468005 | Erb's muscular dystrophy (disorder) |
| 78495000 | Cleft leaflet of mitral valve (disorder) |
| 79439001 | Congenital anomaly of aortic arch (disorder) |
| 80098002 | Diffuse Lewy body disease (disorder) |
| 80387009 | Roger's disease (disorder) |
| 80660001 | Mauriac's syndrome (disorder) |
| 81577001 | Congenital anomaly of inferior vena cava (disorder) |
| 82077006 | Myotubular myopathy (disorder) |
| 82821008 | Congenital atresia of extrahepatic bile duct (disorder) |
| 83119008 | Congenital insufficiency of tricuspid valve (disorder) |
| 83799000 | Corrected transposition of great vessels (disorder) |
| 86252004 | Agenesis of pulmonary artery (disorder) |
| 86299006 | Tetralogy of Fallot (disorder) |
| 86765009 | Mild intellectual disability (disorder) |
| 89392001 | Prader-Willi syndrome (disorder) |
| 89454001 | Shwachman syndrome (disorder) |
| 91634006 | Fused commissures of mitral valve (disorder) |
| 92960007 | Congenital absence of aortic valve (disorder) |
| 92978002 | Congenital absence of thyroid gland (disorder) |
| 93030006 | Congenital absence of spleen (disorder) |
| 93031005 | Congenital atresia of inferior vena cava (disorder) |
| 93059006 | Congenital dilatation of pulmonary artery (disorder) |
| 93153005 | Limb-girdle muscular dystrophy (disorder) |
| 93353003 | Congenital malposition of subclavian artery (disorder) |
| 94706008 | Muscular ventricular septum defect (disorder) |
| 95237001 | Retroesophageal subclavian artery (disorder) |
| 109428005 | Perimembranous ventricular septal defect (disorder) |
| 109432004 | Anomalous cardiac muscle bands (disorder) |
| 109478007 | Kohlschutter's syndrome (disorder) |
| 110359009 | Intellectual disability (disorder) |
| 111307005 | Leprechaunism syndrome (disorder) |
| 111321007 | Right aortic arch (disorder) |
| 111322000 | Congenital anomaly of pulmonary veins (disorder) |
| 111323005 | Total anomalous pulmonary venous return (disorder) |
| 111501005 | Congenital hereditary muscular dystrophy (disorder) |
| 111504002 | Walker-Warburg congenital muscular dystrophy (disorder) |
| 111508004 | Emery-Dreifuss muscular dystrophy (disorder) |
| 123660008 | Dextrorotation of heart (disorder) |
| 191689008 | Active infantile autism (disorder) |
| 191690004 | Residual infantile autism (disorder) |
| 191692007 | Active disintegrative psychoses (disorder) |
| 191693002 | Residual disintegrative psychoses (disorder) |
| 193216006 | Congenital and developmental myasthenia (disorder) |
| 193225000 | Hereditary progressive muscular dystrophy (disorder) |
| 193227008 | Pelvic muscular dystrophy (disorder) |
| 193230001 | Distal muscular dystrophy with juvenile onset (disorder) |
| 197478000 | Congenital celiac disease (disorder) |
| 197601003 | Finnish congenital nephrotic syndrome (disorder) |
| 204296002 | Discordant ventriculoarterial connection (disorder) |
| 204297006 | Total great vessel transposition (disorder) |
| 204299009 | Dextrotransposition of aorta (disorder) |
| 204300001 | Incomplete great vessel transposition (disorder) |
| 204306007 | Pentalogy of Fallot (disorder) |
| 204311009 | Eisenmenger's complex (disorder) |
| 204312002 | Ventricular septal defect between left ventricle and right atrium (disorder) |
| 204318003 | Persistent ostium secundum (disorder) |
| 204319006 | Lutembacher's syndrome (disorder) |
| 204330009 | Common atrioventricular-type ventricular septal defect (disorder) |
| 204339005 | Congenital pulmonary valve abnormality (disorder) |
| 204342004 | Congenital atresia of the pulmonary valve (disorder) |
| 204345002 | Congenital fusion of pulmonic cusps (disorder) |
| 204346001 | Congenital fusion of pulmonary valve segment (disorder) |
| 204351007 | Fallot's trilogy (disorder) |
| 204354004 | Congenital tricuspid atresia and stenosis (disorder) |
| 204357006 | Ebstein's anomaly of tricuspid valve (disorder) |
| 204362007 | Parachute malformation of mitral valve (disorder) |
| 204363002 | Supernumerary cusps of the mitral valve (disorder) |
| 204370002 | Stenosis of infundibulum of right ventricle (disorder) |
| 204378009 | Congenital coronary aneurysm (disorder) |
| 204379001 | Congenital stricture of coronary artery (disorder) |
| 204394002 | Congenital anomaly of myocardium (disorder) |
| 204395001 | Congenital aneurysm of heart (disorder) |
| 204397009 | Cor triloculare (disorder) |
| 204398004 | Congenital epicardial cyst (disorder) |
| 204399007 | Hemicardia (disorder) |
| 204423002 | Anomalous origin of the aortic arch (disorder) |
| 204427001 | Persistent aortic arch convolutions (disorder) |
| 204431007 | Atresia and stenosis of aorta (disorder) |
| 204433005 | Aplasia of aorta (disorder) |
| 204443008 | Pulmonary artery atresia (disorder) |
| 204448004 | Atresia of pulmonary artery with septal defect (disorder) |
| 204451006 | Anomalies of great veins (disorder) |
| 204456001 | Subdiaphragmatic total anomalous pulmonary venous return (disorder) |
| 204457005 | Supradiaphragmatic total anomalous pulmonary venous return (disorder) |
| 204467000 | Pulmonary vein atresia (disorder) |
| 204781002 | Congenital absence of hepatic ducts (disorder) |
| 204782009 | Atresia of hepatic ducts (disorder) |
| 205615000 | Trisomy 21- meiotic nondisjunction (disorder) |
| 205616004 | Trisomy 21- mitotic nondisjunction mosaicism (disorder) |
| 205655003 | Trisomy 22 (disorder) |
| 205769006 | Situs inversus with levocardia (disorder) |
| 205824006 | Noonan's syndrome (disorder) |
| 205834002 | Acardia (disorder) |
| 215677009 | Congenital hypothyroidism with ectopic thyroid (disorder) |
| 217710005 | Congenital iodine deficiency syndrome (disorder) |
| 218728005 | Interrupted aortic arch (disorder) |
| 230291001 | Juvenile Parkinson's disease (disorder) |
| 230292008 | Secondary parkinsonism (disorder) |
| 230296006 | Vascular parkinsonism (disorder) |
| 231536004 | Atypical autism (disorder) |
| 232059000 | Laurence-Moon syndrome (disorder) |
| 233627004 | Congenital cystic bronchiectasis (disorder) |
| 233666007 | Young's syndrome (disorder) |
| 234132006 | Congenital abnormality of great veins and coronary sinus (disorder) |
| 235916001 | Ichthyosis congenita with biliary atresia (disorder) |
| 236383002 | Familial mesangial sclerosis (disorder) |
| 236385009 | Drash syndrome (disorder) |
| 236529001 | Prune belly syndrome with pulmonic stenosis |
| 237227006 | Congenital heart disease in pregnancy (disorder) |
| 237515009 | Congenital hypothyroidism without goiter (disorder) |
| 237516005 | Congenital thyroid hypoplasia (disorder) |
| 237565000 | Congenital iodine deficiency syndrome - mixed type (disorder) |
| 237566004 | Congenital iodine deficiency syndrome - neurological type (disorder) |
| 237616002 | Hypogonadism, diabetes mellitus, alopecia, mental retardation and electrocardiographic abnormalities (disorder) |
| 237617006 | Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness (disorder) |
| 240046001 | Muscular dystrophy with predominantly proximal limb girdle distribution (disorder) |
| 240047005 | X-linked muscular dystrophy with limb girdle distribution (disorder) |
| 240050008 | Manifesting female carrier of X-linked muscular dystrophy (disorder) |
| 240051007 | X-linked limb girdle muscular dystrophy with normal dystrophin (disorder) |
| 240052000 | Ji muscular dystrophy (disorder) |
| 240054004 | Autosomal recessive muscular dystrophy with limb girdle distribution (disorder) |
| 240055003 | Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein (disorder) |
| 240061000 | Congenital muscular dystrophy with arthrogryposis multiplex congenita (disorder) |
| 240062007 | Ullrich congenital muscular dystrophy (disorder) |
| 240067001 | Autosomal dominant muscular dystrophy with limb girdle distribution (disorder) |
| 240069003 | Late onset proximal muscular dystrophy with dysarthria (disorder) |
| 240070002 | Muscular dystrophy not predominantly limb girdle in distribution (disorder) |
| 240071003 | X-linked muscular dystrophy not predominantly limb girdle (disorder) |
| 240072005 | Benign scapuloperoneal muscular dystrophy with cardiomyopathy (disorder) |
| 240073000 | Autosomal recessive muscular dystrophy not predominantly limb girdle (disorder) |
| 240074006 | Scapulohumeral muscular dystrophy (disorder) |
| 240075007 | Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) |
| 240076008 | Benign scapuloperoneal muscular dystrophy (disorder) |
| 240078009 | Benign congenital muscular dystrophy with finger flexion contractures (disorder) |
| 250941001 | Right ventricular fibromuscular infundibular stenosis (disorder) |
| 250942008 | Right ventricular muscular infundibular stenosis (disorder) |
| 250983006 | Bicuspid doming of aortic cusp (disorder) |
| 251038002 | Aortic root congenital abnormality (disorder) |
| 253264007 | Congenital heart disease, septal and bulbar anomalies (disorder) |
| 253267000 | Congenital abnormality of relationship of cardiac component (disorder) |
| 253269002 | Criss-cross heart (disorder) |
| 253271002 | Mirror-imaged heart (disorder) |
| 253272009 | Congenital abnormality of cardiac connection (disorder) |
| 253274005 | Abnormal atrioventricular connection (disorder) |
| 253275006 | Abnormal atrioventricular connection - biventricular (disorder) |
| 253276007 | Cor triloculare biventriculare (disorder) |
| 253277003 | Discordant atrioventricular connection (disorder) |
| 253280002 | Abnormal atrioventricular connection - univentricular (disorder) |
| 253281003 | Double inlet ventricle (disorder) |
| 253282005 | Double inlet right ventricle (disorder) |
| 253283000 | Double inlet left ventricle (disorder) |
| 253286008 | Left sided atrium connecting to left ventricle (disorder) |
| 253289001 | Left sided atrium connecting to ventricle of indeterminate morphology (disorder) |
| 253290005 | Absent left sided atrioventricular connection (disorder) |
| 253291009 | Right sided atrium connecting to right ventricle (disorder) |
| 253294001 | Right sided atrium connecting to ventricle of indeterminate morphology (disorder) |
| 253295000 | Abnormal ventriculoarterial connection (disorder) |
| 253297008 | Transposition of aorta (disorder) |
| 253298003 | Double outlet right ventricle with subaortic ventricular septal defect (disorder) |
| 253300003 | Double outlet right ventricle with doubly committed ventricular septal defect (disorder) |
| 253310007 | Anomalous insertion of right superior vena cava to left atrium (disorder) |
| 253311006 | Bilateral superior vena cava (disorder) |
| 253315002 | Inferior vena cava interruption with bilateral azygos continuation (disorder) |
| 253316001 | Abnormal inferior vena caval connection (disorder) |
| 253320002 | Inferior cava to left of spine with right descending aorta (disorder) |
| 253321003 | Anomalous termination of right pulmonary vein (disorder) |
| 253327004 | Congenital coronary sinus stenosis (disorder) |
| 253329001 | Ductus venosus abnormality (disorder) |
| 253330006 | Patent ductus venosus (disorder) |
| 253334002 | Congenital abnormality of atria and atrial septum (disorder) |
| 253335001 | Isomerism of atrial appendages (disorder) |
| 253336000 | Isomerism of right atrial appendage (disorder) |
| 253337009 | Isomerism of left atrial appendage (disorder) |
| 253341008 | Obstructive Eustachian valve (disorder) |
| 253342001 | Prolapse of Eustachian valve (disorder) |
| 253343006 | Anomalous valve of coronary sinus (disorder) |
| 253348002 | Right atrial endocardial fibroelastosis (disorder) |
| 253349005 | Right atrial hypoplasia (disorder) |
| 253353007 | Divided left atrium (disorder) |
| 253354001 | Supramitral left atrial ring (disorder) |
| 253356004 | Left atrial appendage absent (disorder) |
| 253359006 | Left atrial endocardial fibroelastosis (disorder) |
| 253360001 | Left atrial hypoplasia (disorder) |
| 253364005 | Foramen ovale valvar aneurysm (disorder) |
| 253371000 | Atrial septal defect through coronary sinus orifice (disorder) |
| 253373002 | Atrioventricular septal defect - isolated atrial component (disorder) |
| 253374008 | Congenital abnormality of atrioventricular valves in atrioventricular septal defect (disorder) |
| 253376005 | Tricuspid annulus hypoplasia (disorder) |
| 253377001 | Dilatation of tricuspid annulus (disorder) |
| 253379003 | Straddling tricuspid valve (disorder) |
| 253382008 | Double orifice of tricuspid valve (disorder) |
| 253395003 | Mitral valve dysplasia (disorder) |
| 253396002 | Mitral leaflet dysplasia (disorder) |
| 253404006 | Anterior leaflet of mitral valve attached to septum (disorder) |
| 253405007 | Accessory tissue on mitral leaflet (disorder) |
| 253414002 | Atrioventricular septal defect and common atrioventricular junction (disorder) |
| 253415001 | Atrioventricular septal defect - isolated ventricular component (disorder) |
| 253416000 | Atrioventricular septal defect: atrial and ventricular components (disorder) |
| 253417009 | Atrioventricular septal defect - ventricular component (disorder) |
| 253418004 | Atrioventricular septal defect - ventricular component under superior bridging leaflet (disorder) |
| 253419007 | Atrioventricular septal defect with ventricular component under superior bridging leaflet with chords at crest ventricular septum (disorder) |
| 253511007 | Congenital abnormality of ventricles and ventricular septum (disorder) |
| 253512000 | Tetralogy of Fallot with pulmonary stenosis (disorder) |
| 253513005 | Tetralogy of Fallot with pulmonary atresia (disorder) |
| 253514004 | Dextraposition of aorta in Fallot's tetralogy (disorder) |
| 253515003 | Ventricular septal defect in Fallot's tetralogy (disorder) |
| 253519009 | Hypoplasia of right ventricular inflow tract (disorder) |
| 253523001 | Primary right ventricular endocardial fibroelastosis (disorder) |
| 253524007 | Two chambered right ventricle (disorder) |
| 253525008 | Congenital right ventricular diverticulum (disorder) |
| 253527000 | Congenital right ventricular aneurysm (disorder) |
| 253528005 | Arrhythmogenic right ventricular dysplasia (disorder) |
| 253529002 | Right ventricular outflow tract abnormality (disorder) |
| 253530007 | Right ventricular outflow tract obstruction (disorder) |
| 253531006 | Right ventricular outflow obstruction - localized (disorder) |
| 253532004 | Right ventricular outflow obstruction - tubular (disorder) |
| 253536001 | Left ventricular hypoplasia (disorder) |
| 253539008 | Hypoplasia of left ventricular outflow tract (disorder) |
| 253540005 | Hypoplasia of left ventricular outflow tract and trabecular area (disorder) |
| 253542002 | Abnormal left ventricular muscle band (disorder) |
| 253543007 | Primary left ventricular endocardial fibroelastosis (disorder) |
| 253544001 | Congenital left ventricular aneurysm (disorder) |
| 253545000 | Left ventricular outflow tract abnormality (disorder) |
| 253546004 | Left ventricular outflow tract obstruction (disorder) |
| 253548003 | Indeterminate ventricular outflow tract obstruction (disorder) |
| 253550006 | Multiple ventricular septal defects (disorder) |
| 253551005 | Restrictive ventricular septal defect (disorder) |
| 253552003 | Perimembranous ventricular septal defect with extension to right ventricular inlet (disorder) |
| 253553008 | Perimembranous ventricular septal defect with extension to right ventricular trabecular component (disorder) |
| 253554002 | Perimembranous ventricular septal defect with extension to right ventricular outlet (disorder) |
| 253559007 | Ventricular septal defect with malaligned outlet septum to left (disorder) |
| 253563000 | Muscular ventricular septal defect in inlet septum (disorder) |
| 253564006 | Muscular ventricular septal defect in central trabecular septum (disorder) |
| 253565007 | Muscular ventricular septal defect in apical trabecular septum (disorder) |
| 253566008 | Muscular ventricular septal defect in marginal septum (disorder) |
| 253567004 | Muscular ventricular septal defect in outlet septum (disorder) |
| 253568009 | Doubly committed subarterial ventricular septal defect (disorder) |
| 253569001 | Doubly committed subarterial ventricular septal defect with membranous septum extension (disorder) |
| 253570000 | Doubly committed subarterial ventricular septal defect with muscular posterior inferior rim (disorder) |
| 253571001 | Giant ventricular septal defect (disorder) |
| 253574009 | Subaortic infundibulum (disorder) |
| 253576006 | Bilateral deficient infundibula (disorder) |
| 253578007 | Congenital abnormality of arterial valves (disorder) |
| 253585006 | Pulmonary valve cusp hypoplasia (disorder) |
| 253587003 | Commissural fusion of pulmonary valve (disorder) |
| 253588008 | Pulmonary valve dysplasia (disorder) |
| 253591008 | Pulmonary atresia with ventricular septal defect (disorder) |
| 253593006 | Imperforate pulmonary valve (disorder) |
| 253596003 | Absent pulmonary valve syndrome (disorder) |
| 253597007 | Accessory tissue on pulmonary valve cusp (disorder) |
| 253599005 | Bicuspid pulmonary valve (disorder) |
| 253601007 | Aortic valve ring hypoplasia (disorder) |
| 253603005 | Eccentric opening of aortic valve (disorder) |
| 253607006 | Hypoplasia of aortic valve cusp (disorder) |
| 253608001 | Accessory tissue on aortic valve cusp (disorder) |
| 253609009 | Abnormal number of aortic valve cusps (disorder) |
| 253610004 | Unicuspid aortic valve (disorder) |
| 253611000 | Quadricuspid aortic valve (disorder) |
| 253614008 | Tubular hypoplasia of aorta (disorder) |
| 253615009 | Anomalies of the aorta excluding coarction (disorder) |
| 253629005 | Pulmonary trunk absent with absent pulmonary artery (disorder) |
| 253634009 | Anomalous origin of right pulmonary artery from ascending aorta (disorder) |
| 253638007 | Anomalous origin of left pulmonary artery from right pulmonary artery (disorder) |
| 253643000 | Ascending aortic atresia (disorder) |
| 253646008 | Congenital aneurysm of ascending aorta (disorder) |
| 253652009 | Right descending aorta (disorder) |
| 253654005 | Right aortic arch and right descending aorta (disorder) |
| 253655006 | Right aortic arch and left descending aorta (disorder) |
| 253657003 | Cervical aortic arch (disorder) |
| 253664001 | Vascular ring with right aortic arch (disorder) |
| 253668003 | Isolation of subclavian artery (disorder) |
| 253672004 | Preductal aortic stenosis (disorder) |
| 253673009 | Preductal interruption of aorta (disorder) |
| 253674003 | Preductal hypoplasia of aorta (disorder) |
| 253675002 | Juxtaductal aortic coarctation (disorder) |
| 253676001 | Postductal aortic stenosis (disorder) |
| 253677005 | Postductal interruption of aorta (disorder) |
| 253678000 | Thoracic aortic coarctation (disorder) |
| 253681005 | Interrupted aortic arch distal to left subclavian artery (disorder) |
| 253688004 | Collaterals to pulmonary arteries (disorder) |
| 253689007 | Major aortopulmonary collateral artery (disorder) |
| 253690003 | Systemic to pulmonary collateral artery (disorder) |
| 253691004 | Stenosis of systemic to pulmonary artery collateral artery (disorder) |
| 253700001 | Variant coronary origin from aortic sinus (disorder) |
| 253703004 | Anomalous origin of coronary artery from non-facing sinus (disorder) |
| 253704005 | Anomalous origin of left anterior descending from right coronary artery (disorder) |
| 253706007 | Anomalous origin of coronary artery from pulmonary arterial tree (disorder) |
| 253707003 | Anomalous origin of coronary artery from right pulmonary artery (disorder) |
| 253708008 | Anomalous origin of coronary artery from left pulmonary artery (disorder) |
| 253711009 | Coronary orifice asymmetrical (disorder) |
| 253714001 | Abnormal coronary artery course (disorder) |
| 253715000 | Intramural coronary artery course (disorder) |
| 253716004 | Aberrant course of left anterior descending coronary artery from right coronary artery crossing right ventricular outflow tract (disorder) |
| 253720000 | Congenital coronary arteriovenous fistula (disorder) |
| 253725005 | Congenital coronary artery calcification (disorder) |
| 253728007 | Right dominant coronary system (disorder) |
| 253729004 | Left dominant coronary system (disorder) |
| 253730009 | Balanced coronary system (disorder) |
| 253732001 | Totally absent pericardium (disorder) |
| 253807009 | Intrahepatic biliary atresia (disorder) |
| 254264002 | Partial trisomy 21 in Down's syndrome (disorder) |
| 254268004 | Partial trisomy 13 in Patau's syndrome (disorder) |
| 254734009 | Malignant melanoma arising in congenital nevus (disorder) |
| 263944006 | Anterolateral muscle band (disorder) |
| 263960005 | Bilateral atria (disorder) |
| 264162009 | Posteromedial muscle band (disorder) |
| 264467005 | False tendon - heart (disorder) |
| 264571006 | Septoparietal trabeculations (disorder) |
| 267524009 | Constitutional aplastic anemia with malformation (disorder) |
| 268174004 | Bulbus cordis and cardiac septal closure anomalies (disorder) |
| 268180007 | Right hypoplastic heart syndrome (disorder) |
| 270510008 | Anomalous coronary artery communication (disorder) |
| 271573009 | Congenital abnormality of thoracic aorta and pulmonary arteries (disorder) |
| 274947007 | Divided right atrium (disorder) |
| 276518005 | Transient tricuspid regurgitation of newborn (disorder) |
| 277373000 | Severe childhood autosomal recessive muscular dystrophy (disorder) |
| 278503003 | Congenital hypothyroidism with diffuse goiter (disorder) |
| 278928000 | Transient mitral regurgitation of newborn (disorder) |
| 304576008 | Metaphyseal chondrodysplasia, McKusick type with associated immunodeficiency (disorder) |
| 311808009 | Aberrant retroesophageal subclavian artery causing dysphagia lusoria (disorder) |
| 312991009 | Senile dementia of the Lewy body type (disorder) |
| 360481003 | Common atrioventricular canal (disorder) |
| 373618009 | Autistic spectrum disorder with isolated skills (disorder) |
| 387732009 | Becker muscular dystrophy (disorder) |
| 399091004 | Facioscapulohumeral muscular dystrophy (disorder) |
| 401315004 | Smith-Magenis syndrome (disorder) |
| 408856003 | Autistic disorder (disorder) |
| 408857007 | Infantile autism (disorder) |
| 412787009 | Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth (disorder) |
| 416075005 | On learning disability register (finding) |
| 422348008 | Andersen Tawil syndrome (disorder) |
| 422437002 | X-linked intellectual disability with marfanoid habitus (disorder) |
| 424045003 | Myocardial bridge of coronary artery (disorder) |
| 447780005 | Restrictive interatrial communication with obligatory shunt (disorder) |
| 448794008 | Double outlet right ventricle with subpulmonary ventricular septal defect (disorder) |
| 460437005 | Anomalous origin of dual left anterior descending coronary arteries from right coronary artery and left coronary artery (disorder) |
| 461105005 | Anomalous origin of coronary artery from aorta (disorder) |
| 471286002 | Anomalous origin of coronary artery from aortic sinus to right of nonfacing aortic sinus (disorder) |
| 471291001 | Anomalous origin of right coronary artery from aortic sinus to right of nonfacing aortic sinus and anomalous origin of left coronary artery from aortic sinus to left of nonfacing aortic sinus (disorder) |
| 699311001 | 22q11.2 duplication (disorder) |
| 702344008 | Pitt-Hopkins syndrome (disorder) |
| 702732007 | High-functioning autism (disorder) |
| 702816000 | Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome (disorder) |
| 703535000 | Mowat-Wilson syndrome (disorder) |
| 709469005 | Periodontitis co-occurrent with Down syndrome (disorder) |
| 712884004 | Pathological demand avoidance (disorder) |
| 718572004 | Bethlem myopathy (disorder) |
| 724207001 | Kleefstra syndrome (disorder) |
| 724643004 | Transient abnormal myelopoiesis co-occurrent with Down syndrome (disorder) |
| 724644005 | Myeloid leukemia co-occurrent with Down syndrome (disorder) |
| 726362005 | Partial trisomy of chromosome 22 (disorder) |
| 733194007 | Dementia co-occurrent and due to Down syndrome (disorder) |
| 763186006 | Grubben, De Cock, Borghgraef syndrome (disorder) |
| 763314009 | Congenital muscular dystrophy with hyperlaxity (disorder) |
| 763618001 | Wiedemann Steiner syndrome (disorder) |
| 764512003 | Distal trisomy 22q (disorder) |
| 764524005 | Distal 22q11.2 microduplication syndrome (disorder) |
| 764625002 | Mosaic trisomy 22 syndrome (disorder) |
| 125501000119105 | Fetus with complete trisomy 21 syndrome (disorder) |
| 341751000000103 | Congenital dextroposition of heart (disorder) |
| 508171000000105 | Severe learning disability (disorder) |
| 889211000000104 | Specific learning disability (disorder) |
| 984661000000105 | Mild learning disability (disorder) |
| 984671000000103 | Moderate learning disability (disorder) |
| 984681000000101 | Profound learning disability (disorder) |
Codes not in the full codelist are in faint grey.