Showing entry for Monosomy 13q14 syndrome

General Disease Information
BXGD Id	BXGD024055
Disease Name	Monosomy 13q14 syndrome
Disease CUI Id	C4749304
MeSH Codes	C23   C16
Disease Class Name	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
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