Learning Disability Cardiac
Learning disability and associated cardiac conditions.
Condition group | Dataset | Coding system | Code value | Code description |
---|---|---|---|---|
learning_disability | HES | ICD10 | F803 | Acquired aphasia with epilepsy [Landau-Kleffner] |
learning_disability | HES | ICD10 | F845 | Asperger syndrome |
learning_disability | HES | ICD10 | F841 | Atypical autism |
learning_disability | HES | ICD10 | F840 | Childhood autism |
learning_disability | HES | ICD10 | F819 | Developmental disorder of scholastic skills, unspecified |
learning_disability | HES | ICD10 | F809 | Developmental disorder of speech and language, unspecified |
learning_disability | HES | ICD10 | Q90 | Down syndrome |
learning_disability | HES | ICD10 | Q909 | Down syndrome, unspecified |
learning_disability | HES | ICD10 | F801 | Expressive language disorder |
learning_disability | HES | ICD10 | F70 | Mild mental retardation |
learning_disability | HES | ICD10 | F708 | Mild mental retardation - Other impairments of behaviour |
learning_disability | HES | ICD10 | F701 | Mild mental retardation - Significant impairment of behaviour requiring attention or treatment |
learning_disability | HES | ICD10 | F700 | Mild mental retardation - With the statement of no, or minimal, impairment of behaviour |
learning_disability | HES | ICD10 | F709 | Mild mental retardation - Without mention of impairment of behaviour |
learning_disability | HES | ICD10 | F813 | Mixed disorder of scholastic skills |
learning_disability | HES | ICD10 | F83 | Mixed specific developmental disorders |
learning_disability | HES | ICD10 | F83X | Mixed specific developmental disorders |
learning_disability | HES | ICD10 | F71 | Moderate mental retardation |
learning_disability | HES | ICD10 | F718 | Moderate mental retardation - Other impairments of behaviour |
learning_disability | HES | ICD10 | F711 | Moderate mental retardation - Significant impairment of behaviour requiring attention or treatment |
learning_disability | HES | ICD10 | F710 | Moderate mental retardation - With the statement of no, or minimal, impairment of behaviour |
learning_disability | HES | ICD10 | F719 | Moderate mental retardation - Without mention of impairment of behaviour |
learning_disability | HES | ICD10 | F843 | Other childhood disintegrative disorder |
learning_disability | HES | ICD10 | F818 | Other developmental disorders of scholastic skills |
learning_disability | HES | ICD10 | F808 | Other developmental disorders of speech and language |
learning_disability | HES | ICD10 | F88X | Other disorders of psychological development |
learning_disability | HES | ICD10 | F78 | Other mental retardation |
learning_disability | HES | ICD10 | F788 | Other mental retardation - Other impairments of behaviour |
learning_disability | HES | ICD10 | F781 | Other mental retardation - Significant impairment of behaviour requiring attention or treatment |
learning_disability | HES | ICD10 | F780 | Other mental retardation - With the statement of no, or minimal, impairment of behaviour |
learning_disability | HES | ICD10 | F789 | Other mental retardation - Without mention of impairment of behaviour |
learning_disability | HES | ICD10 | F848 | Other pervasive developmental disorders |
learning_disability | HES | ICD10 | F844 | Overactive disorder associated with mental retardation and stereotyped movements |
learning_disability | HES | ICD10 | F849 | Pervasive developmental disorder, unspecified |
learning_disability | HES | ICD10 | F84 | Pervasive developmental disorders |
learning_disability | HES | ICD10 | F73 | Profound mental retardation |
learning_disability | HES | ICD10 | F738 | Profound mental retardation - Other impairments of behaviour |
learning_disability | HES | ICD10 | F731 | Profound mental retardation - Significant impairment of behaviour requiring attention or treatment |
learning_disability | HES | ICD10 | F730 | Profound mental retardation - With the statement of no, or minimal, impairment of behaviour |
learning_disability | HES | ICD10 | F739 | Profound mental retardation - Without mention of impairment of behaviour |
learning_disability | HES | ICD10 | F802 | Receptive language disorder |
learning_disability | HES | ICD10 | F842 | Rett syndrome |
learning_disability | HES | ICD10 | F72 | Severe mental retardation |
learning_disability | HES | ICD10 | F728 | Severe mental retardation - Other impairments of behaviour |
learning_disability | HES | ICD10 | F721 | Severe mental retardation - Significant impairment of behaviour requiring attention or treatment |
learning_disability | HES | ICD10 | F720 | Severe mental retardation - With the statement of no, or minimal, impairment of behaviour |
learning_disability | HES | ICD10 | F729 | Severe mental retardation - Without mention of impairment of behaviour |
learning_disability | HES | ICD10 | F82 | Specific developmental disorder of motor function |
learning_disability | HES | ICD10 | F82X | Specific developmental disorder of motor function |
learning_disability | HES | ICD10 | F81 | Specific developmental disorders of scholastic skills |
learning_disability | HES | ICD10 | F80 | Specific developmental disorders of speech and language |
learning_disability | HES | ICD10 | F812 | Specific disorder of arithmetical skills |
learning_disability | HES | ICD10 | F810 | Specific reading disorder |
learning_disability | HES | ICD10 | F800 | Specific speech articulation disorder |
learning_disability | HES | ICD10 | F811 | Specific spelling disorder |
learning_disability | HES | ICD10 | Q900 | Trisomy 21, meiotic nondisjunction |
learning_disability | HES | ICD10 | Q901 | Trisomy 21, mosaicism (mitotic nondisjunction) |
learning_disability | HES | ICD10 | Q902 | Trisomy 21, translocation |
learning_disability | HES | ICD10 | F89X | Unspecified disorder of psychological development |
learning_disability | HES | ICD10 | F79 | Unspecified mental retardation |
learning_disability | HES | ICD10 | F798 | Unspecified mental retardation - Other impairments of behaviour |
learning_disability | HES | ICD10 | F791 | Unspecified mental retardation - Significant impairment of behaviour requiring attention or treatment |
learning_disability | HES | ICD10 | F790 | Unspecified mental retardation - With the statement of no, or minimal, impairment of behaviour |
learning_disability | HES | ICD10 | F799 | Unspecified mental retardation - Without mention of impairment of behaviour |
learning_disability | GP data | SNOMED | 50992006 | 22q partial trisomy syndrome (disorder) |
learning_disability | GP data | SNOMED | 699311001 | 22q11.2 duplication (disorder) |
learning_disability | GP data | SNOMED | 17122004 | 4p partial monosomy syndrome (disorder) |
learning_disability | GP data | SNOMED | 70173007 | 5p partial monosomy syndrome (disorder) |
learning_disability | GP data | SNOMED | 14886009 | Abdominal heart (disorder) |
learning_disability | GP data | SNOMED | 253716004 | Aberrant course of left anterior descending coronary artery from right coronary artery crossing right ventricular outflow tract (disorder) |
learning_disability | GP data | SNOMED | 311808009 | Aberrant retroesophageal subclavian artery causing dysphagia lusoria (disorder) |
learning_disability | GP data | SNOMED | 253275006 | Abnormal atrioventricular connection - biventricular (disorder) |
learning_disability | GP data | SNOMED | 253280002 | Abnormal atrioventricular connection - univentricular (disorder) |
learning_disability | GP data | SNOMED | 253274005 | Abnormal atrioventricular connection (disorder) |
learning_disability | GP data | SNOMED | 253714001 | Abnormal coronary artery course (disorder) |
learning_disability | GP data | SNOMED | 253316001 | Abnormal inferior vena caval connection (disorder) |
learning_disability | GP data | SNOMED | 253542002 | Abnormal left ventricular muscle band (disorder) |
learning_disability | GP data | SNOMED | 253609009 | Abnormal number of aortic valve cusps (disorder) |
learning_disability | GP data | SNOMED | 253295000 | Abnormal ventriculoarterial connection (disorder) |
learning_disability | GP data | SNOMED | 253290005 | Absent left sided atrioventricular connection (disorder) |
learning_disability | GP data | SNOMED | 253596003 | Absent pulmonary valve syndrome (disorder) |
learning_disability | GP data | SNOMED | 205834002 | Acardia (disorder) |
learning_disability | GP data | SNOMED | 253608001 | Accessory tissue on aortic valve cusp (disorder) |
learning_disability | GP data | SNOMED | 253405007 | Accessory tissue on mitral leaflet (disorder) |
learning_disability | GP data | SNOMED | 253597007 | Accessory tissue on pulmonary valve cusp (disorder) |
learning_disability | GP data | SNOMED | 66758006 | Acrodysostosis (disorder) |
learning_disability | GP data | SNOMED | 191692007 | Active disintegrative psychoses (disorder) |
learning_disability | GP data | SNOMED | 191689008 | Active infantile autism (disorder) |
learning_disability | GP data | SNOMED | 86252004 | Agenesis of pulmonary artery (disorder) |
learning_disability | GP data | SNOMED | 422348008 | Andersen Tawil syndrome (disorder) |
learning_disability | GP data | SNOMED | 76880004 | Angelman syndrome (disorder) |
learning_disability | GP data | SNOMED | 204451006 | Anomalies of great veins (disorder) |
learning_disability | GP data | SNOMED | 253615009 | Anomalies of the aorta excluding coarction (disorder) |
learning_disability | GP data | SNOMED | 109432004 | Anomalous cardiac muscle bands (disorder) |
learning_disability | GP data | SNOMED | 270510008 | Anomalous coronary artery communication (disorder) |
learning_disability | GP data | SNOMED | 253310007 | Anomalous insertion of right superior vena cava to left atrium (disorder) |
learning_disability | GP data | SNOMED | 75398000 | Anomalous origin of coronary artery (disorder) |
learning_disability | GP data | SNOMED | 461105005 | Anomalous origin of coronary artery from aorta (disorder) |
learning_disability | GP data | SNOMED | 471286002 | Anomalous origin of coronary artery from aortic sinus to right of nonfacing aortic sinus (disorder) |
learning_disability | GP data | SNOMED | 253708008 | Anomalous origin of coronary artery from left pulmonary artery (disorder) |
learning_disability | GP data | SNOMED | 253703004 | Anomalous origin of coronary artery from non-facing sinus (disorder) |
learning_disability | GP data | SNOMED | 253706007 | Anomalous origin of coronary artery from pulmonary arterial tree (disorder) |
learning_disability | GP data | SNOMED | 253707003 | Anomalous origin of coronary artery from right pulmonary artery (disorder) |
learning_disability | GP data | SNOMED | 460437005 | Anomalous origin of dual left anterior descending coronary arteries from right coronary artery and left coronary artery (disorder) |
learning_disability | GP data | SNOMED | 253704005 | Anomalous origin of left anterior descending from right coronary artery (disorder) |
learning_disability | GP data | SNOMED | 253638007 | Anomalous origin of left pulmonary artery from right pulmonary artery (disorder) |
learning_disability | GP data | SNOMED | 68092007 | Anomalous origin of pulmonary artery (disorder) |
learning_disability | GP data | SNOMED | 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) |
learning_disability | GP data | SNOMED | 253634009 | Anomalous origin of right pulmonary artery from ascending aorta (disorder) |
learning_disability | GP data | SNOMED | 204423002 | Anomalous origin of the aortic arch (disorder) |
learning_disability | GP data | SNOMED | 59631007 | Anomalous pulmonary venous drainage (disorder) |
learning_disability | GP data | SNOMED | 253321003 | Anomalous termination of right pulmonary vein (disorder) |
learning_disability | GP data | SNOMED | 253343006 | Anomalous valve of coronary sinus (disorder) |
learning_disability | GP data | SNOMED | 253404006 | Anterior leaflet of mitral valve attached to septum (disorder) |
learning_disability | GP data | SNOMED | 263944006 | Anterolateral muscle band (disorder) |
learning_disability | GP data | SNOMED | 26201005 | Aortic left ventricular tunnel (disorder) |
learning_disability | GP data | SNOMED | 251038002 | Aortic root congenital abnormality (disorder) |
learning_disability | GP data | SNOMED | 253601007 | Aortic valve ring hypoplasia (disorder) |
learning_disability | GP data | SNOMED | 17024001 | Aortopulmonary window (disorder) |
learning_disability | GP data | SNOMED | 204433005 | Aplasia of aorta (disorder) |
learning_disability | GP data | SNOMED | 253528005 | Arrhythmogenic right ventricular dysplasia (disorder) |
learning_disability | GP data | SNOMED | 253643000 | Ascending aortic atresia (disorder) |
learning_disability | GP data | SNOMED | 23560001 | Asperger's disorder (disorder) |
learning_disability | GP data | SNOMED | 68504005 | Ataxia-telangiectasia syndrome (disorder) |
learning_disability | GP data | SNOMED | 204431007 | Atresia and stenosis of aorta (disorder) |
learning_disability | GP data | SNOMED | 204782009 | Atresia of hepatic ducts (disorder) |
learning_disability | GP data | SNOMED | 204448004 | Atresia of pulmonary artery with septal defect (disorder) |
learning_disability | GP data | SNOMED | 253371000 | Atrial septal defect through coronary sinus orifice (disorder) |
learning_disability | GP data | SNOMED | 253373002 | Atrioventricular septal defect - isolated atrial component (disorder) |
learning_disability | GP data | SNOMED | 253415001 | Atrioventricular septal defect - isolated ventricular component (disorder) |
learning_disability | GP data | SNOMED | 253417009 | Atrioventricular septal defect - ventricular component (disorder) |
learning_disability | GP data | SNOMED | 253418004 | Atrioventricular septal defect - ventricular component under superior bridging leaflet (disorder) |
learning_disability | GP data | SNOMED | 253414002 | Atrioventricular septal defect and common atrioventricular junction (disorder) |
learning_disability | GP data | SNOMED | 253419007 | Atrioventricular septal defect with ventricular component under superior bridging leaflet with chords at crest ventricular septum (disorder) |
learning_disability | GP data | SNOMED | 253416000 | Atrioventricular septal defect: atrial and ventricular components (disorder) |
learning_disability | GP data | SNOMED | 231536004 | Atypical autism (disorder) |
learning_disability | GP data | SNOMED | 408856003 | Autistic disorder (disorder) |
learning_disability | GP data | SNOMED | 43614003 | Autistic disorder of childhood onset (disorder) |
learning_disability | GP data | SNOMED | 373618009 | Autistic spectrum disorder with isolated skills (disorder) |
learning_disability | GP data | SNOMED | 240075007 | Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder) |
learning_disability | GP data | SNOMED | 240067001 | Autosomal dominant muscular dystrophy with limb girdle distribution (disorder) |
learning_disability | GP data | SNOMED | 240073000 | Autosomal recessive muscular dystrophy not predominantly limb girdle (disorder) |
learning_disability | GP data | SNOMED | 240055003 | Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein (disorder) |
learning_disability | GP data | SNOMED | 240054004 | Autosomal recessive muscular dystrophy with limb girdle distribution (disorder) |
learning_disability | GP data | SNOMED | 253730009 | Balanced coronary system (disorder) |
learning_disability | GP data | SNOMED | 5619004 | Bardet-Biedl syndrome (disorder) |
learning_disability | GP data | SNOMED | 387732009 | Becker muscular dystrophy (disorder) |
learning_disability | GP data | SNOMED | 240078009 | Benign congenital muscular dystrophy with finger flexion contractures (disorder) |
learning_disability | GP data | SNOMED | 240076008 | Benign scapuloperoneal muscular dystrophy (disorder) |
learning_disability | GP data | SNOMED | 240072005 | Benign scapuloperoneal muscular dystrophy with cardiomyopathy (disorder) |
learning_disability | GP data | SNOMED | 718572004 | Bethlem myopathy (disorder) |
learning_disability | GP data | SNOMED | 72352009 | Bicuspid aortic valve (disorder) |
learning_disability | GP data | SNOMED | 250983006 | Bicuspid doming of aortic cusp (disorder) |
learning_disability | GP data | SNOMED | 253599005 | Bicuspid pulmonary valve (disorder) |
learning_disability | GP data | SNOMED | 263960005 | Bilateral atria (disorder) |
learning_disability | GP data | SNOMED | 253576006 | Bilateral deficient infundibula (disorder) |
learning_disability | GP data | SNOMED | 253311006 | Bilateral superior vena cava (disorder) |
learning_disability | GP data | SNOMED | 4434006 | Bloom syndrome (disorder) |
learning_disability | GP data | SNOMED | 21634003 | Borjeson-Forssman-Lehmann syndrome (disorder) |
learning_disability | GP data | SNOMED | 268174004 | Bulbus cordis and cardiac septal closure anomalies (disorder) |
learning_disability | GP data | SNOMED | 45259000 | Celiac infantilism (disorder) |
learning_disability | GP data | SNOMED | 253657003 | Cervical aortic arch (disorder) |
learning_disability | GP data | SNOMED | 71961003 | Childhood disintegrative disorder (disorder) |
learning_disability | GP data | SNOMED | 78495000 | Cleft leaflet of mitral valve (disorder) |
learning_disability | GP data | SNOMED | 7305005 | Coarctation of aorta (disorder) |
learning_disability | GP data | SNOMED | 26780008 | Coarctation of pulmonary artery (disorder) |
learning_disability | GP data | SNOMED | 15182000 | Coffin-Lowry syndrome (disorder) |
learning_disability | GP data | SNOMED | 10007009 | Coffin-Siris syndrome (disorder) |
learning_disability | GP data | SNOMED | 56604005 | Cohen syndrome (disorder) |
learning_disability | GP data | SNOMED | 253688004 | Collaterals to pulmonary arteries (disorder) |
learning_disability | GP data | SNOMED | 253587003 | Commissural fusion of pulmonary valve (disorder) |
learning_disability | GP data | SNOMED | 73699003 | Common arterial trunk and common origin of pulmonary arteries (disorder) |
learning_disability | GP data | SNOMED | 60106004 | Common arterial trunk and separate origin of pulmonary arteries (disorder) |
learning_disability | GP data | SNOMED | 360481003 | Common atrioventricular canal (disorder) |
learning_disability | GP data | SNOMED | 204330009 | Common atrioventricular-type ventricular septal defect (disorder) |
learning_disability | GP data | SNOMED | 61959006 | Common truncus arteriosus (disorder) |
learning_disability | GP data | SNOMED | 45503006 | Common ventricle (disorder) |
learning_disability | GP data | SNOMED | 26146002 | Complete transposition of great vessels (disorder) |
learning_disability | GP data | SNOMED | 21111006 | Complete trisomy 13 syndrome (disorder) |
learning_disability | GP data | SNOMED | 51500006 | Complete trisomy 18 syndrome (disorder) |
learning_disability | GP data | SNOMED | 41040004 | Complete trisomy 21 syndrome (disorder) |
learning_disability | GP data | SNOMED | 253578007 | Congenital abnormality of arterial valves (disorder) |
learning_disability | GP data | SNOMED | 253334002 | Congenital abnormality of atria and atrial septum (disorder) |
learning_disability | GP data | SNOMED | 253374008 | Congenital abnormality of atrioventricular valves in atrioventricular septal defect (disorder) |
learning_disability | GP data | SNOMED | 253272009 | Congenital abnormality of cardiac connection (disorder) |
learning_disability | GP data | SNOMED | 234132006 | Congenital abnormality of great veins and coronary sinus (disorder) |
learning_disability | GP data | SNOMED | 253267000 | Congenital abnormality of relationship of cardiac component (disorder) |
learning_disability | GP data | SNOMED | 271573009 | Congenital abnormality of thoracic aorta and pulmonary arteries (disorder) |
learning_disability | GP data | SNOMED | 253511007 | Congenital abnormality of ventricles and ventricular septum (disorder) |
learning_disability | GP data | SNOMED | 92960007 | Congenital absence of aortic valve (disorder) |
learning_disability | GP data | SNOMED | 1287007 | Congenital absence of bile duct (disorder) |
learning_disability | GP data | SNOMED | 37687000 | Congenital absence of cervix (disorder) |
learning_disability | GP data | SNOMED | 5230009 | Congenital absence of coronary artery (disorder) |
learning_disability | GP data | SNOMED | 40272001 | Congenital absence of coronary sinus (disorder) |
learning_disability | GP data | SNOMED | 204781002 | Congenital absence of hepatic ducts (disorder) |
learning_disability | GP data | SNOMED | 6996004 | Congenital absence of pulmonary valve (disorder) |
learning_disability | GP data | SNOMED | 93030006 | Congenital absence of spleen (disorder) |
learning_disability | GP data | SNOMED | 92978002 | Congenital absence of thyroid gland (disorder) |
learning_disability | GP data | SNOMED | 193216006 | Congenital and developmental myasthenia (disorder) |
learning_disability | GP data | SNOMED | 16972009 | Congenital aneurysm of aorta (disorder) |
learning_disability | GP data | SNOMED | 253646008 | Congenital aneurysm of ascending aorta (disorder) |
learning_disability | GP data | SNOMED | 204395001 | Congenital aneurysm of heart (disorder) |
learning_disability | GP data | SNOMED | 54160000 | Congenital aneurysm of sinus of Valsalva (disorder) |
learning_disability | GP data | SNOMED | 59877000 | Congenital anomaly of aorta (disorder) |
learning_disability | GP data | SNOMED | 79439001 | Congenital anomaly of aortic arch (disorder) |
learning_disability | GP data | SNOMED | 13689005 | Congenital anomaly of aortic valve (disorder) |
learning_disability | GP data | SNOMED | 28574005 | Congenital anomaly of coronary artery (disorder) |
learning_disability | GP data | SNOMED | 70320004 | Congenital anomaly of heart valve (disorder) |
learning_disability | GP data | SNOMED | 81577001 | Congenital anomaly of inferior vena cava (disorder) |
learning_disability | GP data | SNOMED | 75372006 | Congenital anomaly of mitral valve (disorder) |
learning_disability | GP data | SNOMED | 204394002 | Congenital anomaly of myocardium (disorder) |
learning_disability | GP data | SNOMED | 36110001 | Congenital anomaly of pulmonary artery (disorder) |
learning_disability | GP data | SNOMED | 111322000 | Congenital anomaly of pulmonary veins (disorder) |
learning_disability | GP data | SNOMED | 70195006 | Congenital anomaly of superior vena cava (disorder) |
learning_disability | GP data | SNOMED | 4374004 | Congenital anomaly of tricuspid valve (disorder) |
learning_disability | GP data | SNOMED | 7438000 | Congenital atresia of aorta (disorder) |
learning_disability | GP data | SNOMED | 51442005 | Congenital atresia of aortic valve (disorder) |
learning_disability | GP data | SNOMED | 48520006 | Congenital atresia of cardiac vein (disorder) |
learning_disability | GP data | SNOMED | 82821008 | Congenital atresia of extrahepatic bile duct (disorder) |
learning_disability | GP data | SNOMED | 93031005 | Congenital atresia of inferior vena cava (disorder) |
learning_disability | GP data | SNOMED | 23063005 | Congenital atresia of mitral valve (disorder) |
learning_disability | GP data | SNOMED | 204342004 | Congenital atresia of the pulmonary valve (disorder) |
learning_disability | GP data | SNOMED | 63042009 | Congenital atresia of tricuspid valve (disorder) |
learning_disability | GP data | SNOMED | 77480004 | Congenital biliary atresia (disorder) |
learning_disability | GP data | SNOMED | 77593006 | Congenital bronchiectasis (disorder) |
learning_disability | GP data | SNOMED | 48121000 | Congenital cardiomegaly (disorder) |
learning_disability | GP data | SNOMED | 197478000 | Congenital celiac disease (disorder) |
learning_disability | GP data | SNOMED | 204378009 | Congenital coronary aneurysm (disorder) |
learning_disability | GP data | SNOMED | 253720000 | Congenital coronary arteriovenous fistula (disorder) |
learning_disability | GP data | SNOMED | 253725005 | Congenital coronary artery calcification (disorder) |
learning_disability | GP data | SNOMED | 253327004 | Congenital coronary sinus stenosis (disorder) |
learning_disability | GP data | SNOMED | 233627004 | Congenital cystic bronchiectasis (disorder) |
learning_disability | GP data | SNOMED | 341751000000103 | Congenital dextroposition of heart (disorder) |
learning_disability | GP data | SNOMED | 45237002 | Congenital dilatation of aorta (disorder) |
learning_disability | GP data | SNOMED | 93059006 | Congenital dilatation of pulmonary artery (disorder) |
learning_disability | GP data | SNOMED | 75270000 | Congenital diverticulum of left ventricle (disorder) |
learning_disability | GP data | SNOMED | 37104009 | Congenital enlargement of coronary sinus (disorder) |
learning_disability | GP data | SNOMED | 204398004 | Congenital epicardial cyst (disorder) |
learning_disability | GP data | SNOMED | 204346001 | Congenital fusion of pulmonary valve segment (disorder) |
learning_disability | GP data | SNOMED | 204345002 | Congenital fusion of pulmonic cusps (disorder) |
learning_disability | GP data | SNOMED | 13213009 | Congenital heart disease (disorder) |
learning_disability | GP data | SNOMED | 237227006 | Congenital heart disease in pregnancy (disorder) |
learning_disability | GP data | SNOMED | 253264007 | Congenital heart disease, septal and bulbar anomalies (disorder) |
learning_disability | GP data | SNOMED | 111501005 | Congenital hereditary muscular dystrophy (disorder) |
learning_disability | GP data | SNOMED | 60787001 | Congenital hypoplasia of aortic arch (disorder) |
learning_disability | GP data | SNOMED | 12075007 | Congenital hypoplasia of ascending aorta (disorder) |
learning_disability | GP data | SNOMED | 54682008 | Congenital hypoplasia of pulmonary artery (disorder) |
learning_disability | GP data | SNOMED | 278503003 | Congenital hypothyroidism with diffuse goiter (disorder) |
learning_disability | GP data | SNOMED | 215677009 | Congenital hypothyroidism with ectopic thyroid (disorder) |
learning_disability | GP data | SNOMED | 237515009 | Congenital hypothyroidism without goiter (disorder) |
learning_disability | GP data | SNOMED | 28656008 | Congenital insufficiency of aortic valve (disorder) |
learning_disability | GP data | SNOMED | 29928006 | Congenital insufficiency of mitral valve (disorder) |
learning_disability | GP data | SNOMED | 15096009 | Congenital insufficiency of pulmonary valve (disorder) |
learning_disability | GP data | SNOMED | 83119008 | Congenital insufficiency of tricuspid valve (disorder) |
learning_disability | GP data | SNOMED | 237565000 | Congenital iodine deficiency syndrome - mixed type (disorder) |
learning_disability | GP data | SNOMED | 237566004 | Congenital iodine deficiency syndrome - neurological type (disorder) |
learning_disability | GP data | SNOMED | 217710005 | Congenital iodine deficiency syndrome (disorder) |
learning_disability | GP data | SNOMED | 253544001 | Congenital left ventricular aneurysm (disorder) |
learning_disability | GP data | SNOMED | 51789008 | Congenital malposition of cardiac apex (disorder) |
learning_disability | GP data | SNOMED | 10818008 | Congenital malposition of heart (disorder) |
learning_disability | GP data | SNOMED | 93353003 | Congenital malposition of subclavian artery (disorder) |
learning_disability | GP data | SNOMED | 240061000 | Congenital muscular dystrophy with arthrogryposis multiplex congenita (disorder) |
learning_disability | GP data | SNOMED | 763314009 | Congenital muscular dystrophy with hyperlaxity (disorder) |
learning_disability | GP data | SNOMED | 48796009 | Congenital nephrotic syndrome (disorder) |
learning_disability | GP data | SNOMED | 204339005 | Congenital pulmonary valve abnormality (disorder) |
learning_disability | GP data | SNOMED | 253527000 | Congenital right ventricular aneurysm (disorder) |
learning_disability | GP data | SNOMED | 253525008 | Congenital right ventricular diverticulum (disorder) |
learning_disability | GP data | SNOMED | 36752001 | Congenital splenomegaly (disorder) |
learning_disability | GP data | SNOMED | 11614003 | Congenital stenosis of pulmonary veins (disorder) |
learning_disability | GP data | SNOMED | 45492009 | Congenital stenosis of superior vena cava (disorder) |
learning_disability | GP data | SNOMED | 36233006 | Congenital stenosis of tricuspid valve (disorder) |
learning_disability | GP data | SNOMED | 204379001 | Congenital stricture of coronary artery (disorder) |
learning_disability | GP data | SNOMED | 56118002 | Congenital syphilitic splenomegaly (disorder) |
learning_disability | GP data | SNOMED | 237516005 | Congenital thyroid hypoplasia (disorder) |
learning_disability | GP data | SNOMED | 204354004 | Congenital tricuspid atresia and stenosis (disorder) |
learning_disability | GP data | SNOMED | 28975000 | Constitutional aplastic anemia (disorder) |
learning_disability | GP data | SNOMED | 267524009 | Constitutional aplastic anemia with malformation (disorder) |
learning_disability | GP data | SNOMED | 55510008 | Cor triatriatum (disorder) |
learning_disability | GP data | SNOMED | 204397009 | Cor triloculare (disorder) |
learning_disability | GP data | SNOMED | 253276007 | Cor triloculare biventriculare (disorder) |
learning_disability | GP data | SNOMED | 74218008 | Coronary artery arising from main pulmonary artery (disorder) |
learning_disability | GP data | SNOMED | 253711009 | Coronary orifice asymmetrical (disorder) |
learning_disability | GP data | SNOMED | 83799000 | Corrected transposition of great vessels (disorder) |
learning_disability | GP data | SNOMED | 253269002 | Criss-cross heart (disorder) |
learning_disability | GP data | SNOMED | 12770006 | Cyanotic congenital heart disease (disorder) |
learning_disability | GP data | SNOMED | 40354009 | De Lange syndrome (disorder) |
learning_disability | GP data | SNOMED | 733194007 | Dementia co-occurrent and due to Down syndrome (disorder) |
learning_disability | GP data | SNOMED | 253514004 | Dextraposition of aorta in Fallot's tetralogy (disorder) |
learning_disability | GP data | SNOMED | 27637000 | Dextrocardia (disorder) |
learning_disability | GP data | SNOMED | 123660008 | Dextrorotation of heart (disorder) |
learning_disability | GP data | SNOMED | 204299009 | Dextrotransposition of aorta (disorder) |
learning_disability | GP data | SNOMED | 80098002 | Diffuse Lewy body disease (disorder) |
learning_disability | GP data | SNOMED | 253377001 | Dilatation of tricuspid annulus (disorder) |
learning_disability | GP data | SNOMED | 253277003 | Discordant atrioventricular connection (disorder) |
learning_disability | GP data | SNOMED | 204296002 | Discordant ventriculoarterial connection (disorder) |
learning_disability | GP data | SNOMED | 764524005 | Distal 22q11.2 microduplication syndrome (disorder) |
learning_disability | GP data | SNOMED | 58795000 | Distal muscular dystrophy (disorder) |
learning_disability | GP data | SNOMED | 193230001 | Distal muscular dystrophy with juvenile onset (disorder) |
learning_disability | GP data | SNOMED | 764512003 | Distal trisomy 22q (disorder) |
learning_disability | GP data | SNOMED | 253353007 | Divided left atrium (disorder) |
learning_disability | GP data | SNOMED | 274947007 | Divided right atrium (disorder) |
learning_disability | GP data | SNOMED | 10451007 | Double aortic arch (disorder) |
learning_disability | GP data | SNOMED | 253283000 | Double inlet left ventricle (disorder) |
learning_disability | GP data | SNOMED | 253282005 | Double inlet right ventricle (disorder) |
learning_disability | GP data | SNOMED | 253281003 | Double inlet ventricle (disorder) |
learning_disability | GP data | SNOMED | 253382008 | Double orifice of tricuspid valve (disorder) |
learning_disability | GP data | SNOMED | 7368005 | Double outlet left ventricle (disorder) |
learning_disability | GP data | SNOMED | 7484005 | Double outlet right ventricle (disorder) |
learning_disability | GP data | SNOMED | 253300003 | Double outlet right ventricle with doubly committed ventricular septal defect (disorder) |
learning_disability | GP data | SNOMED | 253298003 | Double outlet right ventricle with subaortic ventricular septal defect (disorder) |
learning_disability | GP data | SNOMED | 448794008 | Double outlet right ventricle with subpulmonary ventricular septal defect (disorder) |
learning_disability | GP data | SNOMED | 253568009 | Doubly committed subarterial ventricular septal defect (disorder) |
learning_disability | GP data | SNOMED | 253569001 | Doubly committed subarterial ventricular septal defect with membranous septum extension (disorder) |
learning_disability | GP data | SNOMED | 253570000 | Doubly committed subarterial ventricular septal defect with muscular posterior inferior rim (disorder) |
learning_disability | GP data | SNOMED | 236385009 | Drash syndrome (disorder) |
learning_disability | GP data | SNOMED | 2593002 | Dubowitz's syndrome (disorder) |
learning_disability | GP data | SNOMED | 76670001 | Duchenne muscular dystrophy (disorder) |
learning_disability | GP data | SNOMED | 253329001 | Ductus venosus abnormality (disorder) |
learning_disability | GP data | SNOMED | 204357006 | Ebstein's anomaly of tricuspid valve (disorder) |
learning_disability | GP data | SNOMED | 253603005 | Eccentric opening of aortic valve (disorder) |
learning_disability | GP data | SNOMED | 78250005 | Ectopia cordis (disorder) |
learning_disability | GP data | SNOMED | 204311009 | Eisenmenger's complex (disorder) |
learning_disability | GP data | SNOMED | 111508004 | Emery-Dreifuss muscular dystrophy (disorder) |
learning_disability | GP data | SNOMED | 75065003 | Endemic cretinism (disorder) |
learning_disability | GP data | SNOMED | 15459006 | Endocardial cushion defect (disorder) |
learning_disability | GP data | SNOMED | 78468005 | Erb's muscular dystrophy (disorder) |
learning_disability | GP data | SNOMED | 399091004 | Facioscapulohumeral muscular dystrophy (disorder) |
learning_disability | GP data | SNOMED | 204351007 | Fallot's trilogy (disorder) |
learning_disability | GP data | SNOMED | 264467005 | False tendon - heart (disorder) |
learning_disability | GP data | SNOMED | 236383002 | Familial mesangial sclerosis (disorder) |
learning_disability | GP data | SNOMED | 125501000119105 | Fetus with complete trisomy 21 syndrome (disorder) |
learning_disability | GP data | SNOMED | 197601003 | Finnish congenital nephrotic syndrome (disorder) |
learning_disability | GP data | SNOMED | 253364005 | Foramen ovale valvar aneurysm (disorder) |
learning_disability | GP data | SNOMED | 91634006 | Fused commissures of mitral valve (disorder) |
learning_disability | GP data | SNOMED | 253571001 | Giant ventricular septal defect (disorder) |
learning_disability | GP data | SNOMED | 763186006 | Grubben, De Cock, Borghgraef syndrome (disorder) |
learning_disability | GP data | SNOMED | 204399007 | Hemicardia (disorder) |
learning_disability | GP data | SNOMED | 193225000 | Hereditary progressive muscular dystrophy (disorder) |
learning_disability | GP data | SNOMED | 702732007 | High-functioning autism (disorder) |
learning_disability | GP data | SNOMED | 19092004 | Holt-Oram syndrome (disorder) |
learning_disability | GP data | SNOMED | 58756001 | Huntington's chorea (disorder) |
learning_disability | GP data | SNOMED | 237616002 | Hypogonadism, diabetes mellitus, alopecia, mental retardation and electrocardiographic abnormalities (disorder) |
learning_disability | GP data | SNOMED | 253607006 | Hypoplasia of aortic valve cusp (disorder) |
learning_disability | GP data | SNOMED | 253539008 | Hypoplasia of left ventricular outflow tract (disorder) |
learning_disability | GP data | SNOMED | 253540005 | Hypoplasia of left ventricular outflow tract and trabecular area (disorder) |
learning_disability | GP data | SNOMED | 253519009 | Hypoplasia of right ventricular inflow tract (disorder) |
learning_disability | GP data | SNOMED | 62067003 | Hypoplastic left heart syndrome (disorder) |
learning_disability | GP data | SNOMED | 235916001 | Ichthyosis congenita with biliary atresia (disorder) |
learning_disability | GP data | SNOMED | 253593006 | Imperforate pulmonary valve (disorder) |
learning_disability | GP data | SNOMED | 204300001 | Incomplete great vessel transposition (disorder) |
learning_disability | GP data | SNOMED | 253548003 | Indeterminate ventricular outflow tract obstruction (disorder) |
learning_disability | GP data | SNOMED | 408857007 | Infantile autism (disorder) |
learning_disability | GP data | SNOMED | 253320002 | Inferior cava to left of spine with right descending aorta (disorder) |
learning_disability | GP data | SNOMED | 253315002 | Inferior vena cava interruption with bilateral azygos continuation (disorder) |
learning_disability | GP data | SNOMED | 1094021000000100 | Intellectual development disorder with minimal impairment of behaviour (disorder) |
learning_disability | GP data | SNOMED | 110359009 | Intellectual disability (disorder) |
learning_disability | GP data | SNOMED | 412787009 | Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth (disorder) |
learning_disability | GP data | SNOMED | 218728005 | Interrupted aortic arch (disorder) |
learning_disability | GP data | SNOMED | 253681005 | Interrupted aortic arch distal to left subclavian artery (disorder) |
learning_disability | GP data | SNOMED | 253807009 | Intrahepatic biliary atresia (disorder) |
learning_disability | GP data | SNOMED | 253715000 | Intramural coronary artery course (disorder) |
learning_disability | GP data | SNOMED | 74034002 | Isolated dextrocardia (disorder) |
learning_disability | GP data | SNOMED | 253668003 | Isolation of subclavian artery (disorder) |
learning_disability | GP data | SNOMED | 253335001 | Isomerism of atrial appendages (disorder) |
learning_disability | GP data | SNOMED | 253337009 | Isomerism of left atrial appendage (disorder) |
learning_disability | GP data | SNOMED | 253336000 | Isomerism of right atrial appendage (disorder) |
learning_disability | GP data | SNOMED | 240052000 | Ji muscular dystrophy (disorder) |
learning_disability | GP data | SNOMED | 230291001 | Juvenile Parkinson's disease (disorder) |
learning_disability | GP data | SNOMED | 253675002 | Juxtaductal aortic coarctation (disorder) |
learning_disability | GP data | SNOMED | 42402006 | Kartagener syndrome (disorder) |
learning_disability | GP data | SNOMED | 724207001 | Kleefstra syndrome (disorder) |
learning_disability | GP data | SNOMED | 109478007 | Kohlschutter's syndrome (disorder) |
learning_disability | GP data | SNOMED | 74561007 | Kommerell's diverticulum (disorder) |
learning_disability | GP data | SNOMED | 240069003 | Late onset proximal muscular dystrophy with dysarthria (disorder) |
learning_disability | GP data | SNOMED | 232059000 | Laurence-Moon syndrome (disorder) |
learning_disability | GP data | SNOMED | 253356004 | Left atrial appendage absent (disorder) |
learning_disability | GP data | SNOMED | 253359006 | Left atrial endocardial fibroelastosis (disorder) |
learning_disability | GP data | SNOMED | 253360001 | Left atrial hypoplasia (disorder) |
learning_disability | GP data | SNOMED | 253729004 | Left dominant coronary system (disorder) |
learning_disability | GP data | SNOMED | 253286008 | Left sided atrium connecting to left ventricle (disorder) |
learning_disability | GP data | SNOMED | 253289001 | Left sided atrium connecting to ventricle of indeterminate morphology (disorder) |
learning_disability | GP data | SNOMED | 253536001 | Left ventricular hypoplasia (disorder) |
learning_disability | GP data | SNOMED | 253545000 | Left ventricular outflow tract abnormality (disorder) |
learning_disability | GP data | SNOMED | 253546004 | Left ventricular outflow tract obstruction (disorder) |
learning_disability | GP data | SNOMED | 41893002 | Left ventricular-right atrial communication (disorder) |
learning_disability | GP data | SNOMED | 111307005 | Leprechaunism syndrome (disorder) |
learning_disability | GP data | SNOMED | 93153005 | Limb-girdle muscular dystrophy (disorder) |
learning_disability | GP data | SNOMED | 204319006 | Lutembacher's syndrome (disorder) |
learning_disability | GP data | SNOMED | 253689007 | Major aortopulmonary collateral artery (disorder) |
learning_disability | GP data | SNOMED | 254734009 | Malignant melanoma arising in congenital nevus (disorder) |
learning_disability | GP data | SNOMED | 240050008 | Manifesting female carrier of X-linked muscular dystrophy (disorder) |
learning_disability | GP data | SNOMED | 80660001 | Mauriac's syndrome (disorder) |
learning_disability | GP data | SNOMED | 237617006 | Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness (disorder) |
learning_disability | GP data | SNOMED | 16567006 | Mesocardia (disorder) |
learning_disability | GP data | SNOMED | 304576008 | Metaphyseal chondrodysplasia, McKusick type with associated immunodeficiency (disorder) |
learning_disability | GP data | SNOMED | 702816000 | Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome (disorder) |
learning_disability | GP data | SNOMED | 1093991000000100 | Mild intellectual development disorder with impairment of behaviour (disorder) |
learning_disability | GP data | SNOMED | 1089831000000100 | Mild intellectual development disorder without significant impairment of behaviour (disorder) |
learning_disability | GP data | SNOMED | 86765009 | Mild intellectual disability (disorder) |
learning_disability | GP data | SNOMED | 984661000000105 | Mild learning disability (disorder) |
learning_disability | GP data | SNOMED | 253271002 | Mirror-imaged heart (disorder) |
learning_disability | GP data | SNOMED | 253396002 | Mitral leaflet dysplasia (disorder) |
learning_disability | GP data | SNOMED | 253395003 | Mitral valve dysplasia (disorder) |
learning_disability | GP data | SNOMED | 61152003 | Moderate intellectual disability (disorder) |
learning_disability | GP data | SNOMED | 984671000000103 | Moderate learning disability (disorder) |
learning_disability | GP data | SNOMED | 764625002 | Mosaic trisomy 22 syndrome (disorder) |
learning_disability | GP data | SNOMED | 703535000 | Mowat-Wilson syndrome (disorder) |
learning_disability | GP data | SNOMED | 253550006 | Multiple ventricular septal defects (disorder) |
learning_disability | GP data | SNOMED | 73297009 | Muscular dystrophy (disorder) |
learning_disability | GP data | SNOMED | 240070002 | Muscular dystrophy not predominantly limb girdle in distribution (disorder) |
learning_disability | GP data | SNOMED | 240046001 | Muscular dystrophy with predominantly proximal limb girdle distribution (disorder) |
learning_disability | GP data | SNOMED | 253565007 | Muscular ventricular septal defect in apical trabecular septum (disorder) |
learning_disability | GP data | SNOMED | 253564006 | Muscular ventricular septal defect in central trabecular septum (disorder) |
learning_disability | GP data | SNOMED | 253563000 | Muscular ventricular septal defect in inlet septum (disorder) |
learning_disability | GP data | SNOMED | 253566008 | Muscular ventricular septal defect in marginal septum (disorder) |
learning_disability | GP data | SNOMED | 253567004 | Muscular ventricular septal defect in outlet septum (disorder) |
learning_disability | GP data | SNOMED | 94706008 | Muscular ventricular septum defect (disorder) |
learning_disability | GP data | SNOMED | 724644005 | Myeloid leukemia co-occurrent with Down syndrome (disorder) |
learning_disability | GP data | SNOMED | 424045003 | Myocardial bridge of coronary artery (disorder) |
learning_disability | GP data | SNOMED | 82077006 | Myotubular myopathy (disorder) |
learning_disability | GP data | SNOMED | 75072002 | Nemaline myopathy (disorder) |
learning_disability | GP data | SNOMED | 205824006 | Noonan's syndrome (disorder) |
learning_disability | GP data | SNOMED | 253341008 | Obstructive Eustachian valve (disorder) |
learning_disability | GP data | SNOMED | 67747009 | Ocular muscular dystrophy (disorder) |
learning_disability | GP data | SNOMED | 77097004 | Oculopharyngeal muscular dystrophy (disorder) |
learning_disability | GP data | SNOMED | 416075005 | On learning disability register (finding) |
learning_disability | GP data | SNOMED | 17718000 | Ostium primum defect (disorder) |
learning_disability | GP data | SNOMED | 63934006 | Overriding aorta (disorder) |
learning_disability | GP data | SNOMED | 204362007 | Parachute malformation of mitral valve (disorder) |
learning_disability | GP data | SNOMED | 62239001 | Parkinson-dementia complex of Guam (disorder) |
learning_disability | GP data | SNOMED | 4223005 | Parkinsonism caused by drug (disorder) |
learning_disability | GP data | SNOMED | 49049000 | Parkinson's disease (disorder) |
learning_disability | GP data | SNOMED | 68237008 | Partial anomalous pulmonary venous connection (disorder) |
learning_disability | GP data | SNOMED | 254268004 | Partial trisomy 13 in Patau's syndrome (disorder) |
learning_disability | GP data | SNOMED | 254264002 | Partial trisomy 21 in Down's syndrome (disorder) |
learning_disability | GP data | SNOMED | 726362005 | Partial trisomy of chromosome 22 (disorder) |
learning_disability | GP data | SNOMED | 253330006 | Patent ductus venosus (disorder) |
learning_disability | GP data | SNOMED | 712884004 | Pathological demand avoidance (disorder) |
learning_disability | GP data | SNOMED | 193227008 | Pelvic muscular dystrophy (disorder) |
learning_disability | GP data | SNOMED | 204306007 | Pentalogy of Fallot (disorder) |
learning_disability | GP data | SNOMED | 109428005 | Perimembranous ventricular septal defect (disorder) |
learning_disability | GP data | SNOMED | 253552003 | Perimembranous ventricular septal defect with extension to right ventricular inlet (disorder) |
learning_disability | GP data | SNOMED | 253554002 | Perimembranous ventricular septal defect with extension to right ventricular outlet (disorder) |
learning_disability | GP data | SNOMED | 253553008 | Perimembranous ventricular septal defect with extension to right ventricular trabecular component (disorder) |
learning_disability | GP data | SNOMED | 709469005 | Periodontitis co-occurrent with Down syndrome (disorder) |
learning_disability | GP data | SNOMED | 204427001 | Persistent aortic arch convolutions (disorder) |
learning_disability | GP data | SNOMED | 38385001 | Persistent left posterior cardinal vein (disorder) |
learning_disability | GP data | SNOMED | 77978002 | Persistent left superior vena cava (disorder) |
learning_disability | GP data | SNOMED | 204318003 | Persistent ostium secundum (disorder) |
learning_disability | GP data | SNOMED | 35919005 | Pervasive developmental disorder (disorder) |
learning_disability | GP data | SNOMED | 702344008 | Pitt-Hopkins syndrome (disorder) |
learning_disability | GP data | SNOMED | 253676001 | Postductal aortic stenosis (disorder) |
learning_disability | GP data | SNOMED | 72242008 | Postductal coarctation of aorta (disorder) |
learning_disability | GP data | SNOMED | 253677005 | Postductal interruption of aorta (disorder) |
learning_disability | GP data | SNOMED | 19972008 | Postencephalitic parkinsonism (disorder) |
learning_disability | GP data | SNOMED | 264162009 | Posteromedial muscle band (disorder) |
learning_disability | GP data | SNOMED | 89392001 | Prader-Willi syndrome (disorder) |
learning_disability | GP data | SNOMED | 253672004 | Preductal aortic stenosis (disorder) |
learning_disability | GP data | SNOMED | 13867009 | Preductal coarctation of aorta (disorder) |
learning_disability | GP data | SNOMED | 253674003 | Preductal hypoplasia of aorta (disorder) |
learning_disability | GP data | SNOMED | 253673009 | Preductal interruption of aorta (disorder) |
learning_disability | GP data | SNOMED | 19249002 | Premature closure of foramen ovale (disorder) |
learning_disability | GP data | SNOMED | 253543007 | Primary left ventricular endocardial fibroelastosis (disorder) |
learning_disability | GP data | SNOMED | 253523001 | Primary right ventricular endocardial fibroelastosis (disorder) |
learning_disability | GP data | SNOMED | 1089731000000100 | Profound intellectual development disorder with impairment of behaviour (disorder) |
learning_disability | GP data | SNOMED | 31216003 | Profound intellectual disability (disorder) |
learning_disability | GP data | SNOMED | 984681000000101 | Profound learning disability (disorder) |
learning_disability | GP data | SNOMED | 253342001 | Prolapse of Eustachian valve (disorder) |
learning_disability | GP data | SNOMED | 236529001 | Prune belly syndrome with pulmonic stenosis |
learning_disability | GP data | SNOMED | 70602002 | Pseudocoarctation of aorta (disorder) |
learning_disability | GP data | SNOMED | 204443008 | Pulmonary artery atresia (disorder) |
learning_disability | GP data | SNOMED | 253591008 | Pulmonary atresia with ventricular septal defect (disorder) |
learning_disability | GP data | SNOMED | 253629005 | Pulmonary trunk absent with absent pulmonary artery (disorder) |
learning_disability | GP data | SNOMED | 253585006 | Pulmonary valve cusp hypoplasia (disorder) |
learning_disability | GP data | SNOMED | 253588008 | Pulmonary valve dysplasia (disorder) |
learning_disability | GP data | SNOMED | 204467000 | Pulmonary vein atresia (disorder) |
learning_disability | GP data | SNOMED | 253611000 | Quadricuspid aortic valve (disorder) |
learning_disability | GP data | SNOMED | 191693002 | Residual disintegrative psychoses (disorder) |
learning_disability | GP data | SNOMED | 191690004 | Residual infantile autism (disorder) |
learning_disability | GP data | SNOMED | 447780005 | Restrictive interatrial communication with obligatory shunt (disorder) |
learning_disability | GP data | SNOMED | 253551005 | Restrictive ventricular septal defect (disorder) |
learning_disability | GP data | SNOMED | 95237001 | Retroesophageal subclavian artery (disorder) |
learning_disability | GP data | SNOMED | 68618008 | Rett's disorder (disorder) |
learning_disability | GP data | SNOMED | 111321007 | Right aortic arch (disorder) |
learning_disability | GP data | SNOMED | 253655006 | Right aortic arch and left descending aorta (disorder) |
learning_disability | GP data | SNOMED | 253654005 | Right aortic arch and right descending aorta (disorder) |
learning_disability | GP data | SNOMED | 253348002 | Right atrial endocardial fibroelastosis (disorder) |
learning_disability | GP data | SNOMED | 253349005 | Right atrial hypoplasia (disorder) |
learning_disability | GP data | SNOMED | 253652009 | Right descending aorta (disorder) |
learning_disability | GP data | SNOMED | 253728007 | Right dominant coronary system (disorder) |
learning_disability | GP data | SNOMED | 268180007 | Right hypoplastic heart syndrome (disorder) |
learning_disability | GP data | SNOMED | 253291009 | Right sided atrium connecting to right ventricle (disorder) |
learning_disability | GP data | SNOMED | 253294001 | Right sided atrium connecting to ventricle of indeterminate morphology (disorder) |
learning_disability | GP data | SNOMED | 250941001 | Right ventricular fibromuscular infundibular stenosis (disorder) |
learning_disability | GP data | SNOMED | 250942008 | Right ventricular muscular infundibular stenosis (disorder) |
learning_disability | GP data | SNOMED | 253531006 | Right ventricular outflow obstruction - localized (disorder) |
learning_disability | GP data | SNOMED | 253532004 | Right ventricular outflow obstruction - tubular (disorder) |
learning_disability | GP data | SNOMED | 253529002 | Right ventricular outflow tract abnormality (disorder) |
learning_disability | GP data | SNOMED | 253530007 | Right ventricular outflow tract obstruction (disorder) |
learning_disability | GP data | SNOMED | 80387009 | Roger's disease (disorder) |
learning_disability | GP data | SNOMED | 240074006 | Scapulohumeral muscular dystrophy (disorder) |
learning_disability | GP data | SNOMED | 39905002 | Scimitar syndrome (disorder) |
learning_disability | GP data | SNOMED | 230292008 | Secondary parkinsonism (disorder) |
learning_disability | GP data | SNOMED | 312991009 | Senile dementia of the Lewy body type (disorder) |
learning_disability | GP data | SNOMED | 264571006 | Septoparietal trabeculations (disorder) |
learning_disability | GP data | SNOMED | 277373000 | Severe childhood autosomal recessive muscular dystrophy (disorder) |
learning_disability | GP data | SNOMED | 1089741000000100 | Severe intellectual development disorder without significant impairment of behaviour (disorder) |
learning_disability | GP data | SNOMED | 40700009 | Severe intellectual disability (disorder) |
learning_disability | GP data | SNOMED | 508171000000105 | Severe learning disability (disorder) |
learning_disability | GP data | SNOMED | 89454001 | Shwachman syndrome (disorder) |
learning_disability | GP data | SNOMED | 21981000 | Single coronary artery (disorder) |
learning_disability | GP data | SNOMED | 205769006 | Situs inversus with levocardia (disorder) |
learning_disability | GP data | SNOMED | 401315004 | Smith-Magenis syndrome (disorder) |
learning_disability | GP data | SNOMED | 889211000000104 | Specific learning disability (disorder) |
learning_disability | GP data | SNOMED | 77956009 | Steinert myotonic dystrophy syndrome (disorder) |
learning_disability | GP data | SNOMED | 204370002 | Stenosis of infundibulum of right ventricle (disorder) |
learning_disability | GP data | SNOMED | 253691004 | Stenosis of systemic to pulmonary artery collateral artery (disorder) |
learning_disability | GP data | SNOMED | 253379003 | Straddling tricuspid valve (disorder) |
learning_disability | GP data | SNOMED | 253574009 | Subaortic infundibulum (disorder) |
learning_disability | GP data | SNOMED | 204456001 | Subdiaphragmatic total anomalous pulmonary venous return (disorder) |
learning_disability | GP data | SNOMED | 204363002 | Supernumerary cusps of the mitral valve (disorder) |
learning_disability | GP data | SNOMED | 204457005 | Supradiaphragmatic total anomalous pulmonary venous return (disorder) |
learning_disability | GP data | SNOMED | 253354001 | Supramitral left atrial ring (disorder) |
learning_disability | GP data | SNOMED | 253690003 | Systemic to pulmonary collateral artery (disorder) |
learning_disability | GP data | SNOMED | 86299006 | Tetralogy of Fallot (disorder) |
learning_disability | GP data | SNOMED | 253513005 | Tetralogy of Fallot with pulmonary atresia (disorder) |
learning_disability | GP data | SNOMED | 253512000 | Tetralogy of Fallot with pulmonary stenosis (disorder) |
learning_disability | GP data | SNOMED | 253678000 | Thoracic aortic coarctation (disorder) |
learning_disability | GP data | SNOMED | 111323005 | Total anomalous pulmonary venous return (disorder) |
learning_disability | GP data | SNOMED | 204297006 | Total great vessel transposition (disorder) |
learning_disability | GP data | SNOMED | 253732001 | Totally absent pericardium (disorder) |
learning_disability | GP data | SNOMED | 724643004 | Transient abnormal myelopoiesis co-occurrent with Down syndrome (disorder) |
learning_disability | GP data | SNOMED | 278928000 | Transient mitral regurgitation of newborn (disorder) |
learning_disability | GP data | SNOMED | 276518005 | Transient tricuspid regurgitation of newborn (disorder) |
learning_disability | GP data | SNOMED | 253297008 | Transposition of aorta (disorder) |
learning_disability | GP data | SNOMED | 36422005 | Transposition of pulmonary veins (disorder) |
learning_disability | GP data | SNOMED | 253376005 | Tricuspid annulus hypoplasia (disorder) |
learning_disability | GP data | SNOMED | 205615000 | Trisomy 21- meiotic nondisjunction (disorder) |
learning_disability | GP data | SNOMED | 205616004 | Trisomy 21- mitotic nondisjunction mosaicism (disorder) |
learning_disability | GP data | SNOMED | 205655003 | Trisomy 22 (disorder) |
learning_disability | GP data | SNOMED | 253614008 | Tubular hypoplasia of aorta (disorder) |
learning_disability | GP data | SNOMED | 253524007 | Two chambered right ventricle (disorder) |
learning_disability | GP data | SNOMED | 2829000 | Uhl's disease (disorder) |
learning_disability | GP data | SNOMED | 240062007 | Ullrich congenital muscular dystrophy (disorder) |
learning_disability | GP data | SNOMED | 253610004 | Unicuspid aortic valve (disorder) |
learning_disability | GP data | SNOMED | 253700001 | Variant coronary origin from aortic sinus (disorder) |
learning_disability | GP data | SNOMED | 230296006 | Vascular parkinsonism (disorder) |
learning_disability | GP data | SNOMED | 66403007 | Vascular ring of aorta (disorder) |
learning_disability | GP data | SNOMED | 253664001 | Vascular ring with right aortic arch (disorder) |
learning_disability | GP data | SNOMED | 204312002 | Ventricular septal defect between left ventricle and right atrium (disorder) |
learning_disability | GP data | SNOMED | 253515003 | Ventricular septal defect in Fallot's tetralogy (disorder) |
learning_disability | GP data | SNOMED | 253559007 | Ventricular septal defect with malaligned outlet septum to left (disorder) |
learning_disability | GP data | SNOMED | 111504002 | Walker-Warburg congenital muscular dystrophy (disorder) |
learning_disability | GP data | SNOMED | 763618001 | Wiedemann Steiner syndrome (disorder) |
learning_disability | GP data | SNOMED | 422437002 | X-linked intellectual disability with marfanoid habitus (disorder) |
learning_disability | GP data | SNOMED | 240051007 | X-linked limb girdle muscular dystrophy with normal dystrophin (disorder) |
learning_disability | GP data | SNOMED | 240071003 | X-linked muscular dystrophy not predominantly limb girdle (disorder) |
learning_disability | GP data | SNOMED | 240047005 | X-linked muscular dystrophy with limb girdle distribution (disorder) |
learning_disability | GP data | SNOMED | 233666007 | Young's syndrome (disorder) |