Showing entry for Spondyloepimetaphyseal Dysplasia, Shohat Type



                               
General Disease Information
BXGD IdBXGD016295
Disease NameSpondyloepimetaphyseal Dysplasia, Shohat Type
Disease CUI IdC1865185
MeSH Codes C16   C05  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations