Showing entry for De Vaal's syndrome

General Disease Information
BXGD Id	BXGD012151
Disease Name	De Vaal's syndrome
Disease CUI Id	C1282908
MeSH Codes	C16   C18   C20   C15
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases; Hemic and Lymphatic Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations