Showing entry for Burnett Schwartz Berberian syndrome

General Disease Information
BXGD Id	BXGD005304
Disease Name	Burnett Schwartz Berberian syndrome
Disease CUI Id	C0263428
MeSH Codes	C16   C17
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id	HP:0001574   HP:0000152   HP:0003549
Human Phenotype Ontology Term	Abnormality of the integument; Abnormality of head or neck; Abnormality of connective tissue
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations