Showing entry for Bruck syndrome 1



                               
General Disease Information
BXGD IdBXGD015118
Disease NameBruck syndrome 1
Disease CUI IdC1850168
MeSH Codes C16   C17   C05  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:225  
Disease Ontology Class Namesyndrome
Disorder Network disorder-protein-compound-food associations