| Disease Browser
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Parent Node:
 Craniofacial Abnormalities (D019465) |
Parent Node:
Dwarfism (D004392) |
Parent Node:
Growth Disorders (D006130) |
Parent Node:
Heart Defects, Congenital (D006330) |
..Starting node
.. Rommen Mueller Sybert syndrome (C535871)
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Child Nodes:
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Sister Nodes: |
..22q11 Deletion Syndrome (D058165)  5
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..Aarskog Syndrome (C535331) 1
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..Al Gazali Aziz Salem syndrome (C535613)
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..Alagille Syndrome (D016738)
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..Amastia, Bilateral, With Ureteral Triplication And Dysmorphism (C566295)
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..Aortic Coarctation (D001017) 3
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..Aortic Valve Disease 1 (C563178) 1
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..Aplasia Cutis Congenita, Congenital Heart Defect, And Frontonasal Cysts (C566997)
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..Arrhythmogenic Right Ventricular Dysplasia (D019571) 13
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..Arterial Occlusive Disease, Progressive, with Hypertension, Heart Defects, Bone Fragility, and Brachysyndactyly (C566529)
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..Baetz-Greenwalt syndrome (C537795)
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..Barth Syndrome (D056889) 2  L: 00399;
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..BEAULIEU-BOYCOTT-INNES SYNDROME (OMIM:613680)
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..Beemer Ertbruggen syndrome (C537668)
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..Bixler Christian Gorlin syndrome (C537632)
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..Blepharophimosis syndrome Ohdo type (C536232)
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..Bonneau Syndrome (C564875)
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..Burn-Mckeown syndrome (C537411)
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..Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies (C563414)
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..Cardiac Valvular Defect, Developmental (C565882)
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..Cardiac valvular dysplasia, X-linked (C535576)
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..Cardioauditory syndrome of Sanchez Cascos (C535577)
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..Cardiocranial syndrome (C535578)
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..Cardiofaciocutaneous syndrome (C535579)
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..Chromosome 1q21.1 Duplication Syndrome (C567290)
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..Chromosome 6pter-P24 Deletion Syndrome (C567239)
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..Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly (C563936)
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..CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA (OMIM:617364)
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..CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER (OMIM:617360)
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..CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2 (OMIM:614980)
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..CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4 (OMIM:615779)
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..Congenital Heart Defects, X-Linked (C567444)
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..Conotruncal cardiac defects (C535464) 1
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..Cor Triatriatum (D003310)
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..Coronary Vessel Anomalies (D003330) 3
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..Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence (C563127)
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..Cranioacrofacial Syndrome (C565147)
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..Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation (C564271)
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..Craniofaciofrontodigital Syndrome (C567298)
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..Crisscross Heart (D003420)
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..Deafness, Congenital Heart Defects, and Posterior Embryotoxon (C566604)
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..Dextrocardia (D003914) 10
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..Distichiasis with Congenital Anomalies of the Heart and Peripheral Vasculature (C565092)
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..Ductus Arteriosus, Patent (D004374) 6
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..Ebstein Anomaly (D004437)
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..Ectopia Cordis (D054083)
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..Ectrodactyly cardiopathy dysmorphism (C536187)
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..Ectrodactyly of Lower Limbs, Congenital Heart Defect, and Micrognathia (C563344)
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..Eisenmenger Complex (D004541)
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..Ellis Yale Winter syndrome (C536205)
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..Emanuel syndrome (C535733)
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..Faciocardiomelic Dysplasia, Lethal (C565578)
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..Faciocardiomelic Syndrome (C567176)
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..Faciocardiorenal syndrome (C536388)
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..Familial anomalous origin of right pulmonary artery (C535681)
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..Fragile Site 16p12 (C565001)
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..Frontoocular Syndrome (C565340)
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..Gay Feinmesser Cohen syndrome (C537676)
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..Genito palato cardiac syndrome (C537683)
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..Growth and Developmental Retardation, Ocular Ptosis, Cardiac Defect, and Anal Atresia (C565755)
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..Heart defects limb shortening (C535850)
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..HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES (OMIM:600001)
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..Heart Septal Defects (D006343) 47
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..Heart-hand syndrome, Slovenian type (C535852)
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..Heart-hand syndrome, Spanish type (C535853)
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..Hecht Scott syndrome (C535856)
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..Heterotaxy Syndrome (D059446) 7
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..Hirschsprung Disease with Heart Defects, Laryngeal Anomalies, and Preaxial Polydactyly (C565817)
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..Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction (C563939)
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..Hittner Hirsch Kreh syndrome (C538323)
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..Ho Kaufman Mcalister syndrome (C538325)
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..Holt-Oram syndrome (C535326)
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..Holzgreve Wagner Rehder syndrome (C535327)
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..Hydrolethalus syndrome (C536079)
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..Hypoplastic Left Heart Syndrome (D018636)
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..Isolated Noncompaction of the Ventricular Myocardium (D056830) 5
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..Kasznica Carlson Coppedge syndrome (C537011)
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..Kleefstra Syndrome (C563043)
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..LEOPARD Syndrome (D044542) 2
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..Levocardia (D007979)
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..Long QT Syndrome (D008133) 20
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..Lowry Maclean syndrome (C537037)
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..Malpuech facial clefting syndrome (C535704)
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..Marcus Gunn phenomenon (C535908)
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..Marfan Syndrome (D008382) 9
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..McDonough syndrome (C538158)
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..McKusick Kaufman syndrome (C538159)
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..McPherson Clemens syndrome (C538160)
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..Mehta Lewis Patton syndrome (C536147)
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..MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS (OMIM:616789)
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..Mexican Cardiomelic Dysplasia (C563087)
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..Microcephaly seizures mental retardation heart disorders (C537544)
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..Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs (C563341)
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..MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS (OMIM:245600)
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..NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART (OMIM:616975)
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..Noncompaction of Left Ventricular Myocardium with Congenital Heart Defects (C564690)
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..Noonan Syndrome (D009634) 12
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..Orstavik Lindemann Solberg syndrome (C537137)
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..Pancreatic Hypoplasia, Congenital, with Diabetes Mellitus and Congenital Heart Disease (C564011)
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..Pilotto syndrome (C537400)
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..Powell Chandra Saal syndrome (C538357)
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..Pseudodiastrophic dysplasia (C535826)
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..Pulmonary Atresia with Intact Ventricular Septum (C562832)
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..Right ventricle hypoplasia (C535682)
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..Rommen Mueller Sybert syndrome (C535871)
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..Saal Bulas syndrome (C537193)
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..Sacral meningocele conotruncal heart defects (C537223)
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..Scimitar Anomaly, Multiple Cardiac Malformations, and Craniofacial and Central Nervous System Abnormalities (C564262)
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..Short QT Syndrome 1 (C566506)
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..Short QT Syndrome 2 (C566505)
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..Short QT Syndrome 3 (C566504)
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..Simpson-Golabi-Behmel syndrome (C537340)
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..Sonoda syndrome (C536680)
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..Steinfeld Syndrome (C566655)
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..Stratton-Parker Syndrome (C566105)
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..Subaortic Stenosis, Membranous (C564793)
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..T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITH OR WITHOUT CARDIAC MALFORMATIONS (OMIM:614868)
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..Tabatznik syndrome (C536784)
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..Tamari Goodman syndrome (C536896)
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..TARP syndrome (C536942)
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..Ter Haar syndrome (C537274)
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..TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE (OMIM:615542)
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..Tetralogy of Fallot (D013771) 4
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..Thomas syndrome (C536514)
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..Transposition of Great Vessels (D014188) 5
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..Tricuspid Atresia (D018785) 1
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..Trilogy of Fallot (D014286)
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..Trisomy 13 Syndrome (D000073839)
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..Trisomy 18 Syndrome (D000073842)
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..Turner Syndrome (D014424) 2
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..Uhl anomaly (C536932)
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..VACTERL association (C536495)
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..VATER association (C536534)
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..Vater Association With Hydrocephalus (C564752)
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..Vater-Like Defects with Pulmonary Hypertension, Laryngeal Webs, and Growth Deficiency (C564244)
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..Ventricular extrasystoles perodactyly Robin sequence (C536537)
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..Verloove-Vanhorick Brubakk syndrome (C536541)
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..Wolff-Parkinson-White Syndrome (D014927)
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..Young Simpson syndrome (C536717)
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..Zunich neuroectodermal syndrome (C536729)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
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