Disease #02333 (DFNA5 (deafness, autosomal dominant, type 5 (DFNA-5)), OMIM:600994)

Official abbreviation DFNA5
Name deafness, autosomal dominant, type 5 (DFNA-5)
OMIM ID 600994
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 1
Associated with 1 gene DFNA5
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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00396825 FR01242660041 Vaché et al., submitted - F no France - - - - - DFNA, DFNA5 - DFNA5 - - 1 David Baux
00396953 FR01242660041/FamS2426 PubMed: Mansard 2022 5-generation family, 16 affected (13F, 3M) F no France - - - - - DFNA, DFNA5 - DFNA5 DFNA5 1 16 David Baux
00396959 FR01210652950/FamS2106 PubMed: Mansard 2022 2-generation family, 8 affected (4F, M, 3 fetuses) M no France - - - - - DFNA5 - DFNA5 DFNA5 1 8 David Baux
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