Showing entry for Ehlers-Danlos syndrome 6B



                               
General Disease Information
BXGD IdBXGD005905
Disease NameEhlers-Danlos syndrome 6B
Disease CUI IdC0268344
MeSH Codes C16   C11   C17   C05  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; 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