Disease #05131 (DFNA51 (deafness, autosomal dominant, type 51 (DFNA-51)), OMIM:613558)

Official abbreviation DFNA51
Name deafness, autosomal dominant, type 51 (DFNA-51)
OMIM ID 613558
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2016-02-18 05:14:45 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00059029 - Karen Avraham laboratory, Tel Aviv university, Israel, unpublished - - no Israel Tunisia;Jewish - - - - DFNA51 High tone hearing loss; variable late onset (20-45y) - TJP2 1 7 Zippi Brownstein
00060264 - PubMed: Walsh 2010, Journal: Walsh 2010 large 4-generation family, 28 affecteds - no Israel Iraq;Jewish - - - - DFNA51 Late onset, progressive, high-tone HL - FAM189A2, TJP2 2 28 Zippi Brownstein
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