Disease Browser
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Parent Node: Cardiovascular Abnormalities (D018376) |
Parent Node: Heart Diseases (D006331) |
..Starting node ..Heart Defects, Congenital (D006330)
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Child Nodes:
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........22q11 Deletion Syndrome (D058165) |
........Aarskog Syndrome (C535331) 1 |
........Al Gazali Aziz Salem syndrome (C535613) |
........Alagille Syndrome (D016738) |
........Amastia, Bilateral, With Ureteral Triplication And Dysmorphism (C566295) |
........Aortic Coarctation (D001017) 3 |
........Aortic Valve Disease (C563178) 1 |
........Aplasia Cutis Congenita, Congenital Heart Defect, And Frontonasal Cysts (C566997) |
........Arrhythmogenic Right Ventricular Dysplasia (D019571) 13 |
........Arterial Occlusive Disease, Progressive, with Hypertension, Heart Defects, Bone Fragility, and Brachysyndactyly (C566529) |
........Baetz-Greenwalt syndrome (C537795) |
........Barth Syndrome (D056889) 2 |
........BEAULIEU-BOYCOTT-INNES SYNDROME (OMIM:613680) |
........Beemer Ertbruggen syndrome (C537668) |
........Bixler Christian Gorlin syndrome (C537632) |
........Blepharophimosis syndrome Ohdo type (C536232) |
........Bonneau Syndrome (C564875) |
........Burn-Mckeown syndrome (C537411) |
........Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies (C563414) |
........Cardiac Valvular Defect, Developmental (C565882) |
........Cardiac valvular dysplasia, X-linked (C535576) |
........Cardioauditory syndrome of Sanchez Cascos (C535577) |
........Cardiocranial syndrome (C535578) |
........Cardiofaciocutaneous syndrome (C535579) |
........Chromosome 1q21.1 Duplication Syndrome (C567290) |
........Chromosome 6pter-P24 Deletion Syndrome (C567239) |
........Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly (C563936) |
........Congenital Heart Defects, X-Linked (C567444) |
........Conotruncal cardiac defects (C535464) 1 |
........Cor Triatriatum (D003310) |
........Coronary Vessel Anomalies (D003330) 3 |
........Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence (C563127) |
........Cranioacrofacial Syndrome (C565147) |
........Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation (C564271) |
........Craniofaciofrontodigital Syndrome (C567298) |
........Crisscross Heart (D003420) |
........Deafness, Congenital Heart Defects, and Posterior Embryotoxon (C566604) |
........Dextrocardia (D003914) 10 |
........Distichiasis with Congenital Anomalies of the Heart and Peripheral Vasculature (C565092) |
........Ductus Arteriosus, Patent (D004374) 6 |
........Ebstein Anomaly (D004437) |
........Ectopia Cordis (D054083) |
........Ectrodactyly cardiopathy dysmorphism (C536187) |
........Ectrodactyly of Lower Limbs, Congenital Heart Defect, and Micrognathia (C563344) |
........Eisenmenger Complex (D004541) |
........Ellis Yale Winter syndrome (C536205) |
........Emanuel syndrome (C535733) |
........Faciocardiomelic Dysplasia, Lethal (C565578) |
........Faciocardiomelic Syndrome (C567176) |
........Faciocardiorenal syndrome (C536388) |
........Familial anomalous origin of right pulmonary artery (C535681) |
........Fragile Site 16p12 (C565001) |
........Frontoocular Syndrome (C565340) |
........Gay Feinmesser Cohen syndrome (C537676) |
........Genito palato cardiac syndrome (C537683) |
........Growth and Developmental Retardation, Ocular Ptosis, Cardiac Defect, and Anal Atresia (C565755) |
........Heart defects limb shortening (C535850) |
........Heart Septal Defects (D006343) 47 |
........Heart-hand syndrome, Slovenian type (C535852) |
........Heart-hand syndrome, Spanish type (C535853) |
........Hecht Scott syndrome (C535856) |
........Heterotaxy Syndrome (D059446) 7 |
........Hirschsprung Disease with Heart Defects, Laryngeal Anomalies, and Preaxial Polydactyly (C565817) |
........Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction (C563939) |
........Hittner Hirsch Kreh syndrome (C538323) |
........Ho Kaufman Mcalister syndrome (C538325) |
........Holt-Oram syndrome (C535326) |
........Holzgreve Wagner Rehder syndrome (C535327) |
........Hydrolethalus syndrome (C536079) |
........Hypoplastic Left Heart Syndrome (D018636) |
........Isolated Noncompaction of the Ventricular Myocardium (D056830) 5 |
........Jarcho-Levin syndrome (C537565) 1 |
........Kasznica Carlson Coppedge syndrome (C537011) |
........Kleefstra Syndrome (C563043) |
........LEOPARD Syndrome (D044542) 2 |
........Levocardia (D007979) |
........Long QT Syndrome (D008133) 20 |
........Lowry Maclean syndrome (C537037) |
........Malpuech facial clefting syndrome (C535704) |
........Marcus Gunn phenomenon (C535908) |
........Marfan Syndrome (D008382) 9 |
........McDonough syndrome (C538158) |
........McKusick Kaufman syndrome (C538159) |
........McPherson Clemens syndrome (C538160) |
........Meacham Syndrome (C563821) |
........Mehta Lewis Patton syndrome (C536147) |
........Mexican Cardiomelic Dysplasia (C563087) |
........Microcephaly seizures mental retardation heart disorders (C537544) |
........Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs (C563341) |
........Noncompaction of Left Ventricular Myocardium with Congenital Heart Defects (C564690) |
........Noonan Syndrome (D009634) 12 |
........Orstavik Lindemann Solberg syndrome (C537137) |
........Pancreatic Hypoplasia, Congenital, with Diabetes Mellitus and Congenital Heart Disease (C564011) |
........Pilotto syndrome (C537400) |
........Powell Chandra Saal syndrome (C538357) |
........Pseudodiastrophic dysplasia (C535826) |
........Pulmonary Atresia with Intact Ventricular Septum (C562832) |
........Right ventricle hypoplasia (C535682) |
........Rommen Mueller Sybert syndrome (C535871) |
........Saal Bulas syndrome (C537193) |
........Sacral meningocele conotruncal heart defects (C537223) |
........Scimitar Anomaly, Multiple Cardiac Malformations, and Craniofacial and Central Nervous System Abnormalities (C564262) |
........Short QT Syndrome 1 (C566506) |
........Short QT Syndrome 2 (C566505) |
........Short QT Syndrome 3 (C566504) |
........Simpson-Golabi-Behmel syndrome (C537340) |
........Sonoda syndrome (C536680) |
........Steinfeld Syndrome (C566655) |
........Stratton-Parker Syndrome (C566105) |
........Subaortic Stenosis, Membranous (C564793) |
........Tabatznik syndrome (C536784) |
........Tamari Goodman syndrome (C536896) |
........TARP syndrome (C536942) |
........Ter Haar syndrome (C537274) |
........Tetralogy of Fallot (D013771) 4 |
........Thomas syndrome (C536514) |
........Transposition of Great Vessels (D014188) 5 |
........Tricuspid Atresia (D018785) 1 |
........Trilogy of Fallot (D014286) |
........Turner Syndrome (D014424) 2 |
........Uhl anomaly (C536932) |
........VACTERL association (C536495) |
........VACTERL association with hydrocephaly, X-linked (C536520) |
........VACTERL hydrocephaly (C536521) |
........VATER association (C536534) |
........Vater Association With Hydrocephalus (C564752) |
........Vater-Like Defects with Pulmonary Hypertension, Laryngeal Webs, and Growth Deficiency (C564244) |
........Ventricular extrasystoles perodactyly Robin sequence (C536537) |
........Verloove-Vanhorick Brubakk syndrome (C536541) |
........Wolff-Parkinson-White Syndrome (D014927) |
........Young Simpson syndrome (C536717) |
........Zunich neuroectodermal syndrome (C536729) |
Sister Nodes: |
..Arrhythmias, Cardiac (D001145) 112
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..Carcinoid Heart Disease (D002275)
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..Cardiac Output, High (D016534)
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..Cardiac Output, Low (D002303)
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..Cardiac Tamponade (D002305)
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..Cardiomegaly (D006332) 46
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..Cardiomyopathies (D009202) 124
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..Endocarditis (D004696) 3
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..Gangliosidosis, Generalized GM1, Type I, with Cardiac Involvement (C566895)
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..Glycogen Storage Disease of Heart, Lethal Congenital (C564888)
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..Heart Aneurysm (D006322)
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..Heart Arrest (D006323) 3
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..Heart Defects, Congenital (D006330) 285
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..Heart Failure (D006333) 5
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..Heart Neoplasms (D006338) 3
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..Heart Rupture (D006341) 2
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..Heart Valve Diseases (D006349) 76
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..Myocardial Ischemia (D017202) 28
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..Pericardial Effusion (D010490) 1
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..Pericarditis (D010493) 3
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..Pneumopericardium (D011026)
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..Postpericardiotomy Syndrome (D011185)
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..Pulmonary Heart Disease (D011660)
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..Rheumatic Heart Disease (D012214)
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..Ventricular Dysfunction (D018754) 4
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..Ventricular Outflow Obstruction (D014694) 44
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..Yorifuji Okuno syndrome (C536714)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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