Showing entry for Chromosome 3, monosomy 3p25

General Disease Information
BXGD Id	BXGD018004
Disease Name	Chromosome 3, monosomy 3p25
Disease CUI Id	C2931337
MeSH Codes	C23
Disease Class Name	Pathological Conditions, Signs and Symptoms
Semantic Type	Cell or Molecular Dysfunction
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations