Showing entry for Aase Smith syndrome 2

General Disease Information
BXGD Id	BXGD018078
Disease Name	Aase Smith syndrome 2
Disease CUI Id	C2931850
MeSH Codes	C16   C15
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic 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