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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Abnormalities, Drug-Induced +   
Abnormalities, Severe Teratoid +   
Absence of Nasal Bones 
Absence of Vagina 
Accessory Pancreas 
Agenesis of Gallbladder  
AICAR Transformylase Inosine Monophosphate Cyclohydrolase Deficiency  
Aicardi syndrome  
Amastia +   
Arrhinia 
Atlanto-Axial Fusion 
Bresheck/Bresek Syndrome 
Cardiovascular Abnormalities +   
Caudal Duplication Anomaly  
chromosomal disease +   
Complete Absence of Bile and Pancreatic Ducts 
Congenital Aural Atresia  
congenital diaphragmatic hernia +   
Congenital Microtia +   
Congenital Stridor 
Crane-Heise Syndrome 
Deal Barratt Dillon Syndrome 
Digestive System Abnormalities +   
Eye Abnormalities +   
Familial Cryptotia 
Familial Laryngeal Web 
Hydrocephalus, Skeletal Anomalies, and Mental Disturbance 
Jaw Diseases +   
Laryngeal Cleft 
Lymphatic Abnormalities +   
Mayer-Rokitansky-Kuster-Hauser syndrome +   
Mondini Dysplasia  
mouth disease +   
Multiple Abnormalities +   
Musculoskeletal Abnormalities +   
Nervous System Malformations +   
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES  
Pancreas Agenesis, Dorsal 
Pharyngeal Diseases +   
Posterior Lumbosacral Vertebral Fusion with Blepharoptosis 
Radiation-Induced Abnormalities 
Renal and Mullerian Duct Hypoplasia +   
Respiratory System Abnormalities +   
Rhiny 
Saito Kuba Tsuruta Syndrome 
Schlegelberger Grote Syndrome 
situs inversus +   
Skin Abnormalities +   
Sprengel Deformity  
Stomatognathic System Abnormalities +   
Congenital structural abnormalities of the mouth and jaws, including the dentition.
Temporomandibular Joint Disorders +   
thyroid malformation +   
tooth disease +   
Urogenital Abnormalities +   
Zaki syndrome  

Synonyms
Exact Synonyms: stomatognathic system abnormality
Primary IDs: MESH:D018640
Definition Sources: MESH:D018640

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