Disease #02352 (DFNA11 (deafness, autosomal dominant, type 11 (DFNA-11)), OMIM:601317)

Official abbreviation DFNA11
Name deafness, autosomal dominant, type 11 (DFNA-11)
OMIM ID 601317
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene MYO7A
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00059026 - Karen Avraham laboratory, Tel Aviv university, Israel, unpublished - - no Israel Jewish-Ashkenazi - - - - DFNA11 postlingual onset, ~5y, profound by age 12; also myopia - MYO7A 1 3 Zippi Brownstein
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