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Ontology Browser

Term:
Aplasia Cutis Congenita, Congenital Heart Defect, and Frontonasal Cysts (DOID:9004128)
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Parent Terms Term With Siblings Child Terms
Cysts +     
22q11 Deletion Syndrome +   
3MC syndrome 3  
Aarskog syndrome +   
Adams-Oliver syndrome +   
ADULT syndrome  
Agenesis of Corpus Callosum with Facial Anomalies and Robin Sequence 
Al Gazali Aziz Salem Syndrome 
Alagille syndrome  
Alves Castelo dos Santos Syndrome 
Anal Sphincter Dysplasia 
Anhidrotic Ectodermal Dysplasia with Immunodeficiency, Osteopetrosis, and Lymphedema  
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome  
Aortic Coarctation +   
aortic valve disease 1  
Aortic Valve Disease 3  
Aplasia Cutis Congenita of Limbs Recessive 
Aplasia Cutis Congenita with Epibulbar Dermoids  
Aplasia Cutis Congenita with Intestinal Lymphangiectasia 
Aplasia Cutis Congenita, Congenital Heart Defect, and Frontonasal Cysts 
Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction 
Arachnoid Cysts +   
AREDYLD Syndrome 
arrhythmogenic right ventricular cardiomyopathy +   
Arthrogryposis and Ectodermal Dysplasia 
Au-Kline Syndrome  
Baetz-Greenwalt syndrome 
Barth syndrome +   
Basan Syndrome  
Beaulieu-Boycott-Innes Syndrome  
Beemer Ertbruggen Syndrome 
Bilateral Amastia with Ureteral Triplication and Dysmorphism 
blepharophimosis-intellectual disability syndrome, SBBYS type  
Bone Cysts +   
Bonneau Syndrome 
Branchioma 
breast cyst +  
Bresheck/Bresek Syndrome 
Bronchogenic Cyst 
Brunoni Syndrome 
Cardiac Malformation, Cleft Lip-Palate, Microcephaly and Digital Anomalies  
Cardiac Valvular Dysplasia, X-Linked  
Cardiac-Urogenital Syndrome  
Cardioauditory Syndrome of Sanchez Cascos 
Cardiocranial Syndrome 
cardiofaciocutaneous syndrome +   
Cerebellar Ataxia Ectodermal Dysplasia 
Charcot Marie Tooth Type 1 Aplasia Cutis Congenita 
choledochal cyst +   
chromosome 1q21.1 duplication syndrome 
chromosome 6pter-p24 deletion syndrome 
Cleft Lip with or without Cleft Palate, Nonsyndromic, 8 
cleft lip-palate-ectodermal dysplasia syndrome  
Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly 
Clouston syndrome  
Colloid Cysts +  
Congenital Ectodermal Dysplasia with Hearing Loss 
CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA  
Congenital Heart Defects, and Other Congenital Anomalies  
CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER  
Congenital Heart Defects, Multiple Types, 2  
Congenital Heart Defects, Multiple Types, 4  
Congenital Heart Defects, Multiple Types, 5  
Congenital Heart Defects, X-Linked +   
Conotruncal Cardiac Defects  
Cor Triatriatum 
Coronary Vessel Anomalies +   
Cranioacrofacial Syndrome 
Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation 
Craniofaciofrontodigital Syndrome 
Crisscross Heart 
Cystic Leukoencephalopathy without Megalencephaly  
Cystic Medial Necrosis of Aorta 
Deafness with Anhidrotic Ectodermal Dysplasia 
Deafness, Congenital Heart Defects, and Posterior Embryotoxon  
Dermatoosteolysis Kirghizian Type 
dermatopathia pigmentosa reticularis  
dermoid cyst +   
Developmental Cardiac Valvular Defect  
dextro-looped transposition of the great arteries +   
dextrocardia +   
Distichiasis with Congenital Anomalies of the Heart and Peripheral Vasculature 
Ebstein anomaly  
Ectodermal Dysplasia 11A, Hypohidrotic/Hair/Tooth Type, Autosomal Dominant  
ECTODERMAL DYSPLASIA 12, HYPOHIDROTIC/HAIR/TOOTH/NAIL TYPE  
ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE  
ECTODERMAL DYSPLASIA 14, HAIR/TOOTH TYPE WITH OR WITHOUT HYPOHIDROSIS  
Ectodermal Dysplasia 4, Hair/Nail Type  
Ectodermal Dysplasia 7, Hair/Nail Type  
Ectodermal Dysplasia 9, Hair/Nail Type  
Ectodermal Dysplasia Adrenal Cyst 
Ectodermal Dysplasia and Neurosensory Deafness 
Ectodermal Dysplasia Mental Retardation Syndactyly 
Ectodermal Dysplasia Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet 
Ectodermal Dysplasia with Natal Teeth, Turnpenny Type 
Ectodermal Dysplasia, Alopecia, Preaxial Polydactyly 
Ectodermal Dysplasia, Ectrodactyly, and Macular Dystrophy  
Ectodermal Dysplasia, Pure Hair-Nail Type 
Ectodermal Dysplasia, Sensorineural Hearing Loss, and Distinctive Facial Features 
Ectodermal Dysplasia, Trichoodontoonychial Type 
Ectodermal Dysplasia-Skin Fragility Syndrome  
Ectodermal Dysplasia-Syndactyly Syndrome +   
ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME  
Ectopia Cordis 
Ectrodactyly and Ectodermal Dysplasia without Cleft Lip/Palate 
Ectrodactyly Cardiopathy Dysmorphism 
Ectrodactyly of Lower Limbs, Congenital Heart Defect, and Micrognathia 
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3  
EEC syndrome +   
Eisenmenger Complex  
Ellis Yale Winter Syndrome 
Ellis-Van Creveld syndrome +   
Emanuel Syndrome 
Epidermal Cyst +  
Esophageal Cyst 
Euhidrotic Ectodermal Dysplasia 
Faciocardiomelic Dysplasia, Lethal 
Faciocardiomelic Syndrome 
Faciocardiorenal Syndrome 
Familial Anomalous Origin of Right Pulmonary Artery 
focal dermal hypoplasia +   
Follicular Cyst +   
Fragile Site 16p12 
Freire-Maia Odontotrichomelic Syndrome 
Frontoocular Syndrome 
Ganglion Cysts 
Gay Feinmesser Cohen Syndrome 
Genito Palato Cardiac Syndrome 
Global Developmental Delay, Lung Cysts, Overgrowth, and Wilms Tumor  
Grange Syndrome  
Growth and Developmental Retardation, Ocular Ptosis, Cardiac Defect, and Anal Atresia 
Halal Setton Wang Syndrome 
Hay Wells Syndrome Recessive Type 
Heart Defects Limb Shortening 
heart septal defect +   
Heart-Hand Syndrome, Slovenian Type  
Heart-Hand Syndrome, Spanish Type 
Hecht Scott Syndrome 
Hidrotic Ectodermal Dysplasia, Autosomal Recessive 
Hidrotic Ectodermal Dysplasia, Christianson-Fourie Type 
Hirschsprung Disease with Heart Defects, Laryngeal Anomalies, and Preaxial Polydactyly 
Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction  
Hittner Hirsch Kreh Syndrome 
Ho Kaufman Mcalister Syndrome 
Holt-Oram syndrome  
Holzgreve-Wagner-Rehder syndrome 
hydrolethalus syndrome +   
hypertelorism, microtia, facial clefting syndrome 
hypohidrotic ectodermal dysplasia +   
hypoplastic left heart syndrome +   
hypoplastic right heart syndrome  
Intellectual Developmental Disorder with Cardiac Defects and Dysmorphic Facies  
Isolated Noncompaction of the Ventricular Myocardium +   
jaw-winking syndrome 
Johanson-Blizzard syndrome  
Jones Hersh Yusk Syndrome 
junctional epidermolysis bullosa with pyloric atresia  
Kasznica Carlson Coppedge Syndrome 
Kleefstra syndrome +   
Ladda Zonana Ramer syndrome 
Larsen-like syndrome B3GAT3 type  
Lelis Syndrome 
LEOPARD syndrome +   
Levocardia 
Linear Skin Defects with Multiple Congenital Anomalies 2  
long QT syndrome +   
Lowry Maclean syndrome 
lymphocele +  
Marfan syndrome +   
Marshall syndrome +   
McDonough Syndrome 
McKusick-Kaufman syndrome  
McPherson Clemens Syndrome 
Meacham Winn Culler Syndrome  
Mediastinal Cysts 
megalencephalic leukoencephalopathy with subcortical cysts +   
Mehta Lewis Patton Syndrome 
meibomian cyst 
Mental Retardation and Distinctive Facial Features with or without Cardiac Defects  
Mesenteric Cyst 
Mexican Cardiomelic Dysplasia 
Microcephaly Seizures Mental Retardation Heart Disorders 
Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs 
Microphthalmia Associated with Colobomatous Cyst 
Mucocele +   
mucocele of salivary gland 
Naegeli-Franceschetti-Jadassohn syndrome  
NEMO Mutation with Immunodeficiency 
Neurocutaneous Syndromes +   
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART  
Noncompaction of Left Ventricular Myocardium with Congenital Heart Defects 
Noonan syndrome +   
Odontomicronychial Dysplasia 
Odontoonychodermal Dysplasia  
Odontotrichoungual-Digital-Palmar Syndrome 
Ohdo syndrome +   
orofacial cleft 7 +   
Orstavik Lindemann Solberg Syndrome  
ovarian cyst +   
pachyonychia congenita +   
palmoplantar keratoderma and congenital alopecia 1  
palmoplantar keratoderma and congenital alopecia 2 
Pancreatic Cyst +   
Papillon-Lefevre disease +   
parovarian cyst 
patent ductus arteriosus +   
Photosensitive Trichothiodystrophy 1  
Pilonidal Sinus  
Pilotto Syndrome 
Pinheiro Freire-Maia Miranda Syndrome 
polycystic liver disease +   
Powell Chandra Saal Syndrome 
Pseudodiastrophic Dysplasia 
Pulmonary Atresia with Intact Ventricular Septum  
Rapp-Hodgkin syndrome  
Right Ventricle Hypoplasia  
Robinson Miller Bensimon Syndrome 
Rommen Mueller Sybert Syndrome 
Rosselli-Gulienetti Syndrome 
Saal Bulas Syndrome 
Sacral Meningocele Conotruncal Heart Defects 
Scimitar Anomaly, Multiple Cardiac Malformations, and Craniofacial and Central Nervous System Abnormalities 
scimitar syndrome +   
Sener Syndrome 
Sensenbrenner syndrome +   
Seres-Santamaria Arimany Muniz Syndrome 
Short QT Syndrome 1  
Short QT Syndrome 2  
Short QT Syndrome 3  
Short Stature, Developmental Delay, and Congenital Heart Defects  
Simpson-Golabi-Behmel syndrome type 1  
Sonoda Syndrome 
spermatocele 
Steinfeld Syndrome 
Stratton-Parker Syndrome 
Structural Heart Defects and Renal Anomalies Syndrome  
Subaortic Stenosis, Membranous 
Synovial Cyst +  
Tabatznik Syndrome 
Tamari Goodman Syndrome 
Tarlov Cysts 
TARP Syndrome  
Taurodontia Absent Teeth Sparse Hair 
Ter Haar Syndrome  
Testicular Anomalies with or without Congenital Heart Disease  
Tetra Amelia with Ectodermal Dysplasia and Lacrimal Duct Abnormalities 
Thomas Syndrome 
Thyroglossal Cyst +  
Trichodental Syndrome 
Trichoodontoonychial Dysplasia 
Trichoscyphodysplasia 
tricuspid atresia +   
Trilogy of Fallot 
Trueb Burg Bottani Syndrome 
Turner syndrome +   
Uhl Anomaly 
Urachal Cyst +  
VACTERL association  
VACTERL/VATER Association with Hydrocephalus  
Van der Woude syndrome +   
Vater-Like Defects with Pulmonary Hypertension, Laryngeal Webs, and Growth Deficiency 
Ventricular Extrasystoles Perodactyly Robin Sequence 
Verloove-Vanhorick Brubakk Syndrome 
visceral heterotaxy +   
Wolff-Parkinson-White syndrome  
Yunis-Varon syndrome  
Zunich Neuroectodermal Syndrome  

Synonyms
Primary IDs: MESH:C566997 ;   RDO:0015187

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.