Disease #02370 (DFNA12 (deafness, autosomal dominant, type 12 (DFNA-12)), OMIM:601543)

Official abbreviation DFNA12
Name deafness, autosomal dominant, type 12 (DFNA-12)
OMIM ID 601543
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene TECTA
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

3 entries on 1 page. Showing entries 1 - 3.
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00059027 - Karen Avraham laboratory, Tel Aviv university, Israel, unpublished - - no Israel Jewish-Ashkenazi - - - - DFNA12 Childhood onset, 2-4y, moderate-severe hearing loss - TECTA 1 3 Zippi Brownstein
00060256 - PubMed: Brownstein 2011, Journal: Brownstein 2011 3-generation family, 5 affecteds (2F, 3M) F;M no Israel Turkey;Jewish - - - - DFNA12 Congenital, progressive, moderate-profound NSHL - TECTA 1 5 Zippi Brownstein
00060257 - Karen Avraham Laboratory - - no Israel Turkey;Jewish - - - - DFNA12 Congenital, progressive, severe-profound NSHL - TECTA 1 2 Zippi Brownstein
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