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Term:
Heart-Hand Syndrome, Slovenian Type (DOID:9003205)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
22q11 Deletion Syndrome +   
3MC syndrome 3  
Aarskog syndrome +   
acheiropody  
acrofacial dysostosis Rodriguez type 
acrofacial dysostosis, Patagonia type 
Acrootoocular Syndrome 
acrorenal syndrome +  
Agenesis of Corpus Callosum with Facial Anomalies and Robin Sequence 
Al Gazali Aziz Salem Syndrome 
Alagille syndrome  
Anonychia-Ectrodactyly 
Anonychia-Onychodystrophy with Hypoplasia or Absence of Distal Phalanges 
Aortic Coarctation +   
aortic valve disease 1  
Aortic Valve Disease 3  
Aplasia Cutis Congenita, Congenital Heart Defect, and Frontonasal Cysts 
arrhythmogenic right ventricular cardiomyopathy +   
Au-Kline Syndrome  
Baetz-Greenwalt syndrome 
Banki Syndrome 
Barth syndrome +   
Beaulieu-Boycott-Innes Syndrome  
Beemer Ertbruggen Syndrome 
Bilateral Amastia with Ureteral Triplication and Dysmorphism 
blepharophimosis-intellectual disability syndrome, SBBYS type  
Bonneau Syndrome 
brachydactyly type E1  
brachydactyly type E2  
Camptodactyly 1 
Camptodactyly Joint Contractures and Facial Skeletal Dysplasia 
Camptodactyly Syndrome Guadalajara Type 1 
Camptodactyly Syndrome Guadalajara Type 2 
Camptodactyly Taurinuria 
Camptodactyly Vertebral Fusion 
Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia 
camptodactyly-arthropathy-coxa vara-pericarditis syndrome  
Camptodactyly-Ichthyosis Syndrome 
camptodactyly-tall stature-scoliosis-hearing loss syndrome  
Camptosynpolydactyly, Complex  
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 +   
Carnevale Hernandez Castillo Syndrome 
Catel Manzke Syndrome  
Chitayat Meunier Hodgkinson Syndrome 
chromosome 1q21.1 duplication syndrome 
chromosome 6pter-p24 deletion syndrome 
Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly 
Coffin-Siris syndrome +   
cold-induced sweating syndrome +   
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 
Craniosynostosis, Adelaide Type 
Crisscross Heart 
Daneman Davy Mancer Syndrome 
Deafness, Congenital Heart Defects, and Posterior Embryotoxon  
Deafness, Congenital Onychodystrophy, Recessive Form 
Developmental Cardiac Valvular Defect  
dextro-looped transposition of the great arteries +   
dextrocardia +   
Digitorenocerebral Syndrome  
Digitotalar Dysmorphism 
Distal Symphalangism +   
Distichiasis with Congenital Anomalies of the Heart and Peripheral Vasculature 
Dwarfism Stiff Joint Ocular Abnormalities 
Dystelephalangy 
Ebstein anomaly  
Ectodermal Dysplasia, Ectrodactyly, and Macular Dystrophy  
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  
Ectrodactyly-Cleft Palate Syndrome 
Eiken Skeletal Dysplasia  
Eisenmenger Complex  
Ellis Yale Winter Syndrome 
Emanuel Syndrome 
Extensor Tendons of Fingers, Anomalous Insertion of 
Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly 
Faciocardiomelic Dysplasia, Lethal 
Faciocardiomelic Syndrome 
Faciocardiorenal Syndrome 
Fairbank Disease 
Familial Anomalous Origin of Right Pulmonary Artery 
Femur Bifid with Monodactylous Ectrodactyly 
Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome 
Fragile Site 16p12 
Frints De Smet Fabry Fryns Syndrome 
Frontoocular Syndrome 
Frontootopalatodigital Osteodysplasia 
Fuhrmann syndrome  
Gay Feinmesser Cohen Syndrome 
Genito Palato Cardiac Syndrome 
Gingival Fibromatosis with Hypertrichosis and Mental Retardation 
Goodman Camptodactyly 
Gordon Syndrome  
Grange Syndrome  
Growth and Developmental Retardation, Ocular Ptosis, Cardiac Defect, and Anal Atresia 
Growth Mental Deficiency Syndrome of Myhre  
Growth Retardation, Small and Puffy Hands and Feet, and Eczema 
Hairy Palms and Soles 
hand-foot-genital syndrome  
Heart Defects Limb Shortening 
heart septal defect +   
Heart-Hand Syndrome, Slovenian Type  
Heart-Hand Syndrome, Spanish Type 
Hecht Scott Syndrome 
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 
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate  
Holt-Oram syndrome  
Holzgreve-Wagner-Rehder syndrome 
hydrolethalus syndrome +   
hypertelorism, microtia, facial clefting syndrome 
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 
Johnson Munson Syndrome 
Kasznica Carlson Coppedge Syndrome 
Keutel Syndrome  
Khalifa Graham Syndrome 
Kleefstra syndrome +   
Larsen-like syndrome B3GAT3 type  
Laurin-Sandrow syndrome  
LEOPARD syndrome +   
Leri Pleonosteosis 
Levocardia 
long QT syndrome +   
Lowry Maclean syndrome 
Macrodactyly of the Hand 
Mammary-Digital-Nail Syndrome 
Marfan syndrome +   
McDonough Syndrome 
McKusick-Kaufman syndrome  
McPherson Clemens Syndrome 
Meacham Winn Culler Syndrome  
Mehta Lewis Patton Syndrome 
Mental Retardation and Distinctive Facial Features with or without Cardiac Defects  
Metacarpal 4 5 Fusion  
Metaphyseal Acroscyphodysplasia 
Mexican Cardiomelic Dysplasia 
Michels Caskey Syndrome 
Microcephaly Seizures Mental Retardation Heart Disorders 
Microcephaly with Mental Retardation and Digital Anomalies  
Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs 
Mononen-Karnes-Senac syndrome 
Morillo-Cucci Passarge Syndrome 
Muller Barth Menger Syndrome 
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART  
Neurofaciodigitorenal Syndrome 
Noncompaction of Left Ventricular Myocardium with Congenital Heart Defects 
Noonan syndrome +   
Oculootoradial Syndrome  
Odontotrichoungual-Digital-Palmar Syndrome 
Ohdo syndrome +   
Oroacral Syndrome, Verloes-Koulischer Type 
Orstavik Lindemann Solberg Syndrome  
Oslam syndrome 
Oto-Palato-Digital Syndrome Type 1  
Oto-Palato-Digital Syndrome, Type 2  
Otopalatodigital Spectrum Disorder  
Partial Aphalangia with Syndactyly and Duplication of Metatarsal IV 
patent ductus arteriosus +   
Patent Ductus Arteriosus and Bicuspid Aortic Valve with Hand Anomalies 
Pfeiffer Tietze Welte Syndrome 
Pilotto Syndrome 
Postaxial Polydactyly, with Dental and Vertebral Anomalies 
Powell Chandra Saal Syndrome 
Progeroid Facial Appearance with Hand Anomalies 
Pseudodiastrophic Dysplasia 
Pseudotrisomy 13 Syndrome 
Pulmonary Atresia with Intact Ventricular Septum  
Radio-Ulnar Synostosis Type 1 
Radio-Ulnar Synostosis Type 2 
Rhizomelic Dysplasia Patterson Lowry Type 
Richieri Costa Guion-Almeida Syndrome 
Richieri Costa Pereira Syndrome  
Right Ventricle Hypoplasia  
Rommen Mueller Sybert Syndrome 
Rozin Hertz Goodman Syndrome 
Saal Bulas Syndrome 
Sacral Meningocele Conotruncal Heart Defects 
Sanderson Fraser Syndrome 
Say Field Coldwell syndrome 
Schinzel-Giedion Syndrome  
Scimitar Anomaly, Multiple Cardiac Malformations, and Craniofacial and Central Nervous System Abnormalities 
scimitar syndrome +   
Second Metatarsal-Metacarpal 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 
Split Hand Split Foot Nystagmus 
split hand-foot malformation 1 with sensorineural hearing loss  
Spondylocamptodactyly 
Steinfeld Syndrome 
Stoll Alembik Dott Syndrome 
Stratton-Parker Syndrome 
Structural Heart Defects and Renal Anomalies Syndrome  
Subaortic Stenosis, Membranous 
Symphalangism with Multiple Anomalies of Hands and Feet 
Symphalangism, C. S. Lewis Type 
Synostosis, Carpal, with Dysplastic Elbow Joints and Brachydactyly  
Synpolydactyly 2  
Tabatznik Syndrome 
Tamari Goodman Syndrome 
TARP Syndrome  
tarsal-carpal coalition syndrome  
Teebi Kaurah Syndrome 
Teebi Syndrome 
Tel Hashomer Camptodactyly Syndrome 
Ter Haar Syndrome  
Terminal Osseous Dysplasia and Pigmentary Defects  
Testicular Anomalies with or without Congenital Heart Disease  
Thomas Syndrome 
Tollner Horst Manzke Syndrome 
trichorhinophalangeal syndrome type III  
tricuspid atresia +   
Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet 
Trilogy of Fallot 
Triphalangeal Thumb +   
Tukel Syndrome 
Turner syndrome +   
Uhl Anomaly 
Unilateral Adactylia 
Unilateral Aplasia of Extensor Muscles of Fingers, with Generalized Polyneuropathy 
VACTERL association  
VACTERL/VATER Association with Hydrocephalus  
Van Maldergem syndrome +   
Vater-Like Defects with Pulmonary Hypertension, Laryngeal Webs, and Growth Deficiency 
Ventricular Extrasystoles Perodactyly Robin Sequence 
Verloove-Vanhorick Brubakk Syndrome 
visceral heterotaxy +   
Vohwinkel syndrome  
Walbaum Titran Durieux Crepin Syndrome 
Weaver syndrome  
Weyers Ulnar Ray/Oligodactyly Syndrome 
Wolff-Parkinson-White syndrome  
Zimmerman Laband Syndrome  
Zunich Neuroectodermal Syndrome  

Synonyms
Primary IDs: MESH:C535852 ;   RDO:0001187
Alternate IDs: OMIM:610140

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