Showing entry for Spondyloepiphyseal dysplasia, Omani type



                               
General Disease Information
BXGD IdBXGD014256
Disease NameSpondyloepiphyseal dysplasia, Omani type
Disease CUI IdC1837657
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 DOID:7  
Disease Ontology Class Namedisease of anatomical entity
Disorder Network disorder-protein-compound-food associations