Disease #02351 (DFNA10 (deafness, autosomal dominant, type 10 (DFNA10)), OMIM:601316)

Official abbreviation DFNA10
Name deafness, autosomal dominant, type 10 (DFNA10)
OMIM ID 601316
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene EYA4
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-11-19 10:21:06 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00059025 - Karen Avraham laboratory, Tel Aviv university, Israel, unpublished - - no Israel Lybia;Jewish-Ashkenazi - - - - DFNA10 postlingual, onset 5-12y, progresses to severe-profound hearing loss - EYA4 1 3 Zippi Brownstein
00377113 175355 - - F no Germany - - - - - DFNA10 Abnormality of the inner ear, Sensorineural hearing impairment, Functional abnormality of the inner ear EYA4 EYA4 1 1 Andreas Laner
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