Disease #00148 (DFNA-17 (deafness, autosomal dominant, type 17 (DFNA-17)), OMIM:603622)

Official abbreviation DFNA-17
Name deafness, autosomal dominant, type 17 (DFNA-17)
OMIM ID 603622
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MYH9
Associated tissues -
Disease features autosomal dominant
Remarks -

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