Disease #06950 (DFNA78 (deafness, autosomal dominant, type 78), OMIM:619081)

Official abbreviation DFNA78
Name deafness, autosomal dominant, type 78
OMIM ID 619081
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene SLC12A2
Associated tissues -
Disease features -
Remarks -
Date created 2022-08-05 13:48:54 +02:00 (CEST)
Date last edited N/A


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00428680 Fam35 PubMed: Wonkam 2022 3-generation family, 6 affected (3M,3F) M no Ghana Africa - - - - DFNA78 - - SLC12A2 1 6 Yacouba Dia
00448507 - - - M - Pakistan - - - - - DFNA78 - SLC12A2 SLC12A2 1 1 Hina Khan
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