Showing entry for Deafness, Autosomal Dominant 9

General Disease Information
BXGD Id	BXGD013842
Disease Name	Deafness, Autosomal Dominant 9
Disease CUI Id	C1832425
MeSH Codes	C23   C10   C09
Disease Class Name	Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
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