Showing entry for Distal arthrogryposis syndrome



                               
General Disease Information
BXGD IdBXGD005464
Disease NameDistal arthrogryposis syndrome
Disease CUI IdC0265213
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   HP:0003549   HP:0003011  
Human Phenotype Ontology TermAbnormality of the skeletal system; Abnormality of connective tissue; Abnormality of the musculature
Disease Ontology Id DOID:7  
Disease Ontology Class Namedisease of anatomical entity
Disorder Network disorder-protein-compound-food associations