Showing entry for Congenital thrombocytopenia

General Disease Information
BXGD Id	BXGD006335
Disease Name	Congenital thrombocytopenia
Disease CUI Id	C0272278
MeSH Codes	C23   C16   C20   C15
Disease Class Name	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id	HP:0001871
Human Phenotype Ontology Term	Abnormality of blood and blood-forming tissues
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations