Showing entry for Deafness, Autosomal Dominant 12

General Disease Information
BXGD Id	BXGD013809
Disease Name	Deafness, Autosomal Dominant 12
Disease CUI Id	C1832187
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