Disease #02355 (DFNA9 (deafness, autosomal dominant, type 9 (DFNA-9)), OMIM:601369)

Official abbreviation DFNA9
Name deafness, autosomal dominant, type 9 (DFNA-9)
OMIM ID 601369
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 COCH
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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00059030 - Karen Avraham laboratory, Tel Aviv university, Israel, unpublished - - no Israel Jewish-Ashkenazi - - - - DFNA9 Late onset (18-30y), progressive high-tone hearing loss - COCH 1 3 Zippi Brownstein
00100385 - - - - - Netherlands - - - - - DFNA9 - COCH COCH 1 1 Margit Schraders
00428417 Fam36 PubMed: Wonkam 2022 4-generation family, 4 affected (2F, 2M), unaffected heterozygous carrier relatives M no Ghana Africa - - - - DFNA9 - - OTOF 1 4 Yacouba Dia
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