Showing entry for Romano-Ward Syndrome

General Disease Information
BXGD Id	BXGD002566
Disease Name	Romano-Ward Syndrome
Disease CUI Id	C0035828
MeSH Codes	C23   C16   C14
Disease Class Name	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; 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