Showing entry for DEAFNESS, DIGENIC, GJB2/GJB6 (disorder)

General Disease Information
BXGD Id	BXGD017225
Disease Name	DEAFNESS, DIGENIC, GJB2/GJB6 (disorder)
Disease CUI Id	C2673760
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