Showing entry for Osteogenesis imperfecta, dominant perinatal lethal

General Disease Information
BXGD Id	BXGD005913
Disease Name	Osteogenesis imperfecta, dominant perinatal lethal
Disease CUI Id	C0268358
MeSH Codes	C16   C17   C05
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
Semantic Type	Disease or Syndrome; Congenital Abnormality
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630   DOID:7
Disease Ontology Class Name	genetic disease; disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations