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EXPERIMENTAL FACTOR ONTOLOGY - ANNOTATIONS

Term:cardiogenetic disease
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Accession:EFO:MONDO:0100547 term browser browse the term
Definition:A heterogeneous group of genetic conditions, with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology that are characterized by abnormalities in the cardiovascular system.
Synonyms:exact_synonym: hereditary heart disease
 alt_id: MONDO:0100547


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Term paths to the root
Path 1
Term Annotations click to browse term
  experimental factor 0
    material property 0
      disposition 0
        disease 0
          genetic disorder 0
            cardiogenetic disease 0
              8q24.3 microdeletion syndrome 0
              Alagille syndrome + 0
              Brugada syndrome + 0
              CHARGE syndrome 0
              CHIME syndrome 0
              COG1-congenital disorder of glycosylation 0
              Char syndrome 0
              Ehlers-Danlos syndrome, cardiac valvular type 0
              Ehlers-Danlos syndrome, musculocontractural type 0
              Ellis-van Creveld syndrome 0
              GATA6-related congenital heart disease with or without pancreatic agenesis or neonatal diabetes + 0
              Holt-Oram syndrome + 0
              LMNA-related cardiocutaneous progeria syndrome 0
              Larsen-like syndrome, B3GAT3 type 0
              MGAT2-congenital disorder of glycosylation 0
              PDA1 0
              Peters plus syndrome 0
              Sengers syndrome 0
              TARP syndrome 0
              alveolar capillary dysplasia with misalignment of pulmonary veins 0
              atrial conduction disease 0
              atrial heart septal defect + 0
              atrioventricular block + 0
              autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome 0
              cardiac anomalies - developmental delay - facial dysmorphism syndrome 0
              cardiac valvular dysplasia, X-linked 0
              congenital heart defects, multiple types, 3 0
              congenital heart defects, multiple types, 5 0
              congenital vertebral-cardiac-renal anomalies syndrome + 0
              coronary artery disease, autosomal dominant 2 0
              dextro-looped transposition of the great arteries + 0
              dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome 0
              familial atrial fibrillation + 0
              familial atrial myxoma 0
              familial atrioventricular septal defect + 0
              familial bicuspid aortic valve 0
              familial cardiomyopathy + 0
              familial long QT syndrome + 0
              familial retinal arterial macroaneurysm 0
              familial sick sinus syndrome + 0
              heart defects-limb shortening syndrome 0
              hypoplastic left heart syndrome + 0
              inherited mitral valve disease + 0
              orthostatic intolerance 0
              patent ductus arteriosus 2 0
              patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome 0
              pericardial effusion, chronic 0
              progressive familial heart block + 0
              pulmonary hypertension, primary, autosomal recessive 0
              severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome 0
              short QT syndrome + 0
              sinoatrial node dysfunction and deafness 0
              structural congenital heart disease, multiple types - GATA4 + 0
              supravalvular aortic stenosis 0
              transketolase deficiency 0
              tricuspid atresia 0
              ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome 0
              ventricular fibrillation, paroxysmal familial, type 1 0
              ventricular septal defect + 0
              ventricular tachycardia, familial + 0
Path 2
Term Annotations click to browse term
  experimental factor 0
    material property 0
      disposition 0
        disease 0
          cardiovascular disease 0
            heart disease 0
              cardiogenetic disease 0
                8q24.3 microdeletion syndrome 0
                Alagille syndrome + 0
                Brugada syndrome + 0
                CHARGE syndrome 0
                CHIME syndrome 0
                COG1-congenital disorder of glycosylation 0
                Char syndrome 0
                Ehlers-Danlos syndrome, cardiac valvular type 0
                Ehlers-Danlos syndrome, musculocontractural type 0
                Ellis-van Creveld syndrome 0
                GATA6-related congenital heart disease with or without pancreatic agenesis or neonatal diabetes + 0
                Holt-Oram syndrome + 0
                LMNA-related cardiocutaneous progeria syndrome 0
                Larsen-like syndrome, B3GAT3 type 0
                MGAT2-congenital disorder of glycosylation 0
                PDA1 0
                Peters plus syndrome 0
                Sengers syndrome 0
                TARP syndrome 0
                alveolar capillary dysplasia with misalignment of pulmonary veins 0
                atrial conduction disease 0
                atrial heart septal defect + 0
                atrioventricular block + 0
                autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome 0
                cardiac anomalies - developmental delay - facial dysmorphism syndrome 0
                cardiac valvular dysplasia, X-linked 0
                congenital heart defects, multiple types, 3 0
                congenital heart defects, multiple types, 5 0
                congenital vertebral-cardiac-renal anomalies syndrome + 0
                coronary artery disease, autosomal dominant 2 0
                dextro-looped transposition of the great arteries + 0
                dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome 0
                familial atrial fibrillation + 0
                familial atrial myxoma 0
                familial atrioventricular septal defect + 0
                familial bicuspid aortic valve 0
                familial cardiomyopathy + 0
                familial long QT syndrome + 0
                familial retinal arterial macroaneurysm 0
                familial sick sinus syndrome + 0
                heart defects-limb shortening syndrome 0
                hypoplastic left heart syndrome + 0
                inherited mitral valve disease + 0
                orthostatic intolerance 0
                patent ductus arteriosus 2 0
                patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome 0
                pericardial effusion, chronic 0
                progressive familial heart block + 0
                pulmonary hypertension, primary, autosomal recessive 0
                severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome 0
                short QT syndrome + 0
                sinoatrial node dysfunction and deafness 0
                structural congenital heart disease, multiple types - GATA4 + 0
                supravalvular aortic stenosis 0
                transketolase deficiency 0
                tricuspid atresia 0
                ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome 0
                ventricular fibrillation, paroxysmal familial, type 1 0
                ventricular septal defect + 0
                ventricular tachycardia, familial + 0
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