Disease #02580 (DFNA-22 (deafness, autosomal dominant, type 22 (DFNA-22)), OMIM:606346)

Official abbreviation DFNA-22
Name deafness, autosomal dominant, type 22 (DFNA-22)
OMIM ID 606346
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene MYO6
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Individuals

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00059028 - - - - no Israel Ashkenazi Jew - 0 - - DFNA-22 Teen onset (12-17y), moderate-profound hearing loss - MYO6 1 3 Zippi Brownstein
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