Showing entry for Osteochondrodysplasias



                               
General Disease Information
BXGD IdBXGD002142
Disease NameOsteochondrodysplasias
Disease CUI IdC0029422
MeSH Codes C16   C05  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id HP:0000924  
Human Phenotype Ontology TermAbnormality of the skeletal system
Disease Ontology Id DOID:0014667   DOID:630   DOID:7  
Disease Ontology Class Namedisease of metabolism; genetic disease; disease of anatomical entity
Disorder Network disorder-protein-compound-food associations