Showing entry for Marfan Syndrome, Type I

General Disease Information
BXGD Id	BXGD023778
Disease Name	Marfan Syndrome, Type I
Disease CUI Id	C4721845
MeSH Codes	C16   C17   C05   C14
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:7
Disease Ontology Class Name	disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations