Showing entry for Autosomal dominant macrothrombocytopenia

General Disease Information
BXGD Id	BXGD022570
Disease Name	Autosomal dominant macrothrombocytopenia
Disease CUI Id	C4304021
MeSH Codes	C16
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630   DOID:7
Disease Ontology Class Name	genetic disease; disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations