Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources

Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Aase Smith Syndrome 
Abruzzo-Erickson syndrome  
Acromegaloid Facial Appearance Syndrome 
acromesomelic dysplasia-3  
acromicric dysplasia +   
Acropectoral Syndrome 
Adams-Oliver syndrome +   
ADULT syndrome  
Agenesis of Corpus Callosum with Facial Anomalies and Robin Sequence 
Arachnodactyly +   
Atelosteogenesis Type 3  
B-Cell Immunodeficiency, Distal Limb Anomalies, and Urogenital Malformations  
Bagatelle Cassidy Syndrome 
brachydactyly +   
Brachymorphism-Onychodysplasia-Dysphalangism Syndrome 
Brachyolmia Type 1, Hobaek Type 
Calabro Syndrome 
Camptobrachydactyly 
Cardioacrofacial Dysplasia +   
Cartwright Nelson Fryns Syndrome 
Cerebrorenodigital Syndrome with Limb Malformations and Triradiate Acetabula 
CHILD syndrome  
CHITAYAT SYNDROME  
congenital limbs-face contractures-hypotonia-developmental delay syndrome  
Congenital Upper Extremity Deformities +   
Craniomicromelic Syndrome 
Diaphragmatic Defects, Limb Deficiencies, and Ossification Defects Of Skull 
Distal Transverse Limb Defects with Mental Retardation and Spasticity 
Ectrodactyly-Polydactyly 
Ectromelia +   
ENDOVE SYNDROME, LIMB-BRAIN TYPE  
Feingold syndrome +   
fetal akinesia deformation sequence syndrome X-linked 
fetal encasement syndrome  
Freire-Maia Odontotrichomelic Syndrome 
Fryns Syndrome  
Grubben de Cock Borghgraef Syndrome 
Hand and Foot Deformity with Flat Facies 
Hanhart Syndrome 
Heart Defects Limb Shortening 
hypochondroplasia  
Hypoglossia-Hypodactylia 
Ichthyosis Tapered Fingers Midline Groove Up 
Intellectual Developmental Disorder with Dysmorphic Facies, Seizures, and Distal Limb Anomalies  
Kaplan Plauchu Fitch Syndrome 
Kaufman oculocerebrofacial syndrome  
Kuster Syndrome 
Laryngeal Atresia, Encephalocele, and Limb Deformities 
Le Marec Bracq Picaud Syndrome 
Lethal Faciocardiomelic Dysplasia 
Limb-Mammary Syndrome  
Lower Extremity Deformities, Congenital +   
Lynch Lee Murday syndrome 
Malformation of Arms 
Megalodactyly  
Mental Retardation Spasticity Ectrodactyly 
Mesomelia-Synostoses Syndrome 
Metaphyseal Anadysplasia +   
Microphthalmia with Cyst, Bilateral Facial Clefts, and Limb Anomalies 
Multiple Epiphyseal Dysplasia with Robin Phenotype 
Multiple Pterygium Syndrome, X-Linked 
Nephrosis with Deafness and Urinary Tract and Digital Malformations 
Neu-Laxova syndrome 1  
NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES  
NEURODEVELOPMENTAL, JAW, EYE, AND DIGITAL SYNDROME  
Nievergelt Syndrome 
Palant Cleft Palate Syndrome 
Penttinen-Aula Syndrome  
Peters plus syndrome  
Pointer Syndrome 
polydactyly +   
postaxial acrofacial dysostosis  
Powell Chandra Saal Syndrome 
Proteus syndrome +   
Radial Ray Deficiency, X-Linked 
Radiohumeral Fusions with Other Skeletal and Craniofacial Anomalies  
rapadilino syndrome  
Reardon Hall Slaney syndrome 
Renal Dysplasia - Limb Defects Syndrome 
Robinow syndrome +   
Ruzicka Goerz Anton syndrome 
Short Stature-Obesity Syndrome 
Splenogonadal Fusion with Limb Defects and Micrognathia 
split hand-foot malformation +   
Split-Foot Malformation with Mesoaxial Polydactyly  
Split-Hand with Obstructive Uropathy, Spina Bifida, and Diaphragmatic Defects 
Steinfeld Syndrome 
Stern Lubinsky Durrie Syndrome 
Stratton-Parker Syndrome 
syndactyly +   
syndromic microphthalmia 6  
Tetramelic Monodactyly 
Tetramelic Postaxial Oligodactyly 
thanatophoric dysplasia +   
Thoracic Dysplasia-Hydrocephalus Syndrome 
Thoraco Limb Dysplasia Rivera Type 
Thoracomelic Dysplasia 
Ulnar Hypoplasia with Mental Retardation 
VACTERL association +   
Viljoen Kallis Voges Syndrome 
Weill-Marchesani Syndrome 3  
Weyers acrofacial dysostosis  
Wright Dyck Syndrome 
Yunis-Varon syndrome  

Synonyms
Exact Synonyms: Sommer-Hines syndrome
Primary IDs: MESH:C566066
Alternate IDs: OMIM:187510
Xrefs: GARD:3707 ;   MONDO:0008544 ;   ORDO:2564

paths to the root