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Ontology Browser

Term:
Cardioauditory Syndrome of Sanchez Cascos (DOID:9005076)
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Parent Terms Term With Siblings Child Terms
Deafness +     
22q11 Deletion Syndrome +   
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome  
3MC syndrome 3  
Aarskog syndrome +   
Absence of Tibia with Congenital Deafness 
acrocardiofacial syndrome 
Agenesis of Corpus Callosum with Facial Anomalies and Robin Sequence 
Al Gazali Aziz Salem Syndrome 
Alagille syndrome +   
Albinism Deafness Syndrome 
Aortic Coarctation +   
aortic valve disease 1  
aortic valve disease 3  
Aortico-Ventricular Tunnel 
Aplasia Cutis Congenita, Congenital Heart Defect, and Frontonasal Cysts 
arrhythmogenic right ventricular cardiomyopathy +   
Arthrogryposis Multiplex with Deafness, Inguinal Hernias, and Early Death 
autosomal dominant congenital deafness with onychodystrophy  
autosomal dominant nonsyndromic deafness 65  
Ayazi Syndrome 
Baetz-Greenwalt Syndrome 
Barth syndrome +   
Beaulieu-Boycott-Innes Syndrome  
Beemer Ertbruggen Syndrome 
Bilateral Amastia with Ureteral Triplication and Dysmorphism 
Bonneau Syndrome 
Branchiogenic-Deafness Syndrome 
Burn-McKeown syndrome  
Cardiac Valvular Dysplasia +   
Cardiac-Urogenital Syndrome  
Cardioacrofacial Dysplasia +   
Cardioauditory Syndrome of Sanchez Cascos 
Cardiocranial Syndrome 
cardiofaciocutaneous syndrome +   
Cardiofacioneurodevelopmental Syndrome  
CHIME syndrome  
chromosome 1q21.1 duplication syndrome  
chromosome 6pter-p24 deletion syndrome 
cleft palate, cardiac defects, and intellectual disabillity  
COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS  
Congenital Deafness and Familial Myoclonic Epilepsy 
Congenital Deafness, with Vitiligo and Achalasia 
Congenital Emphysema, with Deafness, Penoscrotal Web, and Mental Retardation 
CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA  
CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME  
congenital heart defects, dysmorphic facial features, and intellectual developmental disorder  
congenital heart defects, hamartomas of tongue, and polysyndactyly  
Congenital Heart Defects, Multiple Types +   
Congenital Heart Defects, X-Linked +   
Congenital Myopathy with Neuropathy and Deafness  
Conotruncal Cardiac Defects  
Cor Triatriatum 
Coronary Vessel Anomalies +   
Coxoauricular Syndrome 
Cranioacrofacial Syndrome 
Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation 
Craniofaciofrontodigital Syndrome 
Crisscross Heart 
Davenport Donlan Syndrome 
Deaf-Blind Disorders +   
Deafness Hyperuricemia Neurologic Ataxia 
Deafness with Anhidrotic Ectodermal Dysplasia 
Deafness, Autosomal Dominant, due to Mutation In Myo1a 
DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY  
Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities 
Deafness, Congenital Heart Defects, and Posterior Embryotoxon  
Deafness, Congenital Onychodystrophy, Recessive Form 
DEAFNESS, CONGENITAL, AND ADULT-ONSET PROGRESSIVE LEUKOENCEPHALOPATHY  
Deafness, with Smith-Magenis Syndrome  
dextro-looped transposition of the great arteries +   
dextrocardia +   
Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, and Mental Retardation 
Distichiasis with Congenital Anomalies of the Heart and Peripheral Vasculature 
Ebstein anomaly  
Ectopia Cordis 
Ectrodactyly Cardiopathy Dysmorphism 
Ectrodactyly of Lower Limbs, Congenital Heart Defect, and Micrognathia 
Eisenmenger Complex  
Ellis Yale Winter Syndrome 
Emanuel Syndrome 
Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness 
Faciocardiomelic Syndrome 
Faciocardiorenal Syndrome 
Familial Anomalous Origin of Right Pulmonary Artery 
Fine-Lubinsky Syndrome  
Fountain Syndrome 
Frank-Ter Haar syndrome  
Frontoocular Syndrome 
Gay Feinmesser Cohen Syndrome 
Genito Palato Cardiac Syndrome 
Grange Syndrome  
Growth and Developmental Retardation, Ocular Ptosis, Cardiac Defect, and Anal Atresia 
Heart Defects Limb Shortening 
heart septal defect +   
Heart-Hand Syndrome, Slovenian Type  
Hecht Scott Syndrome 
hereditary spastic paraplegia 24 
Herrmann Syndrome 
high myopia-sensorineural deafness syndrome  
Hirschsprung Disease with Heart Defects, Laryngeal Anomalies, and Preaxial Polydactyly 
Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 
Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction  
Hittner Hirsch Kreh Syndrome  
Ho Kaufman Mcalister Syndrome 
Holt-Oram syndrome +   
Holzgreve-Wagner-Rehder syndrome 
hydrolethalus syndrome +   
Hyperlipoproteinemia Type II, and Deafness 
hypertelorism, microtia, facial clefting syndrome 
HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS 
Hypokalemic Tubulopathy and Deafness  
hypoplastic left heart syndrome +   
hypoplastic right heart syndrome  
Intellectual Developmental Disorder with Cardiac Defects and Dysmorphic Facies  
Isolated Noncompaction of the Ventricular Myocardium +   
ITM2B-related cerebral amyloid angiopathy 2  
jaw-winking syndrome  
Johnson Neuroectodermal Syndrome 
Jones Syndrome 
Kasznica Carlson Coppedge Syndrome 
Keipert syndrome  
Keratitis-Ichthyosis-Deafness Syndrome +   
Kleefstra syndrome +   
Konigsmark Knox Hussels Syndrome 
Larsen-like syndrome B3GAT3 type  
Lethal Faciocardiomelic Dysplasia 
LEUKOENCEPHALOPATHY, PROGRESSIVE, INFANTILE-ONSET, WITH OR WITHOUT DEAFNESS  
Levocardia 
long QT syndrome +   
Lowry Maclean syndrome 
Lynch Lee Murday syndrome 
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome  
Marfan syndrome +   
McDonough Syndrome 
McKusick-Kaufman syndrome  
McPherson Clemens Syndrome 
Meacham Winn Culler Syndrome  
Mehta Lewis Patton Syndrome 
Membranous Subaortic Stenosis 
Mental Retardation and Distinctive Facial Features with or without Cardiac Defects  
Mexican Cardiomelic Dysplasia 
Meyenburg-Altherr-Uehlinger Syndrome 
Microcephaly Deafness Syndrome 
Microcephaly Seizures Mental Retardation Heart Disorders 
Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs 
Muckle-Wells syndrome  
multiple synostoses syndrome 1  
Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders 
Myoclonus, Cerebellar Ataxia, and Deafness 
Nathalie Syndrome 
Nephrosis with Deafness and Urinary Tract and Digital Malformations 
Neurodevelopmental Disorder with or without Anomalies of the Brain, Eye, or Heart  
Noncompaction of Left Ventricular Myocardium with Congenital Heart Defects 
Noninsulin-Dependent Diabetes Mellitus with Deafness  
nonsyndromic deafness +   
Noonan syndrome +   
Noonan syndrome with multiple lentigines +   
Ohdo syndrome +   
Opticocochleodentate Degeneration 
pancreatic hypoplasia-diabetes-congenital heart disease syndrome  
patent ductus arteriosus +   
Perrault syndrome +   
Pilotto Syndrome 
Powell Chandra Saal Syndrome 
Pseudodiastrophic Dysplasia 
Pulmonary Atresia with Intact Ventricular Septum  
Ramos Arroyo Clark Syndrome 
Ribbonlike Corneal Degeneration with Deafness 
Richards-Rundle Syndrome 
Right Ventricle Hypoplasia  
Rommen Mueller Sybert Syndrome 
Saal Bulas Syndrome 
Sacral Meningocele Conotruncal Heart Defects 
Schimke X-Linked Mental Retardation Syndrome 
Schlegelberger Grote Syndrome 
scimitar syndrome +   
Secretory Diarrhea, Myopathy, and Deafness 
Short QT Syndrome 1  
Short QT Syndrome 2  
Short QT Syndrome 3  
Short Stature, Developmental Delay, and Congenital Heart Defects  
Siddiqi syndrome  
Simpson-Golabi-Behmel syndrome type 1  
Sinoatrial Node Dysfunction and Deafness  
Sonoda Syndrome 
spastic paraplegia with deafness 
Steinfeld Syndrome 
Stratton-Parker Syndrome 
Structural Heart Defects and Renal Anomalies Syndrome  
Tabatznik Syndrome 
Tamari Goodman Syndrome 
TARP syndrome  
temtamy preaxial brachydactyly syndrome  
Testicular Anomalies with or without Congenital Heart Disease  
Thomas Syndrome 
Tietz syndrome  
tricuspid atresia +   
Trilogy of Fallot 
Turner syndrome +   
Uhl Anomaly 
VACTERL association +   
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  
Wright Dyck Syndrome 
X-linked Alport syndrome  
X-linked cardiac valvular dysplasia  
X-linked mental retardation Gustavson type  
X-linked mental retardation-hypotonic facies syndrome-1  
X-linked retinitis pigmentosa and sinorespiratory infections  
Yemenite Deaf-Blind Hypopigmentation Syndrome 

Synonyms
Exact Synonyms: Sanchez Cascos cardioauditory syndrome
Primary IDs: MESH:C535577
Alternate IDs: MIM:212100

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