Disease #03170 (DFNA-2B (deafness, autosomal dominant, type 2b (DFNA-2B)), OMIM:612644)

Official abbreviation DFNA-2B
Name deafness, autosomal dominant, type 2b (DFNA-2B)
OMIM ID 612644
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene GJB3
Associated tissues -
Disease features -
Remarks -

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