Showing entry for Genee-Wiedemann syndrome



                               
General Disease Information
BXGD IdBXGD005486
Disease NameGenee-Wiedemann syndrome
Disease CUI IdC0265257
MeSH Codes C16   C11   C05   C07  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Musculoskeletal Diseases; Stomatognathic Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:630  
Disease Ontology Class Namegenetic disease
Disorder Network disorder-protein-compound-food associations