Disease #02580 (DFNA22 (deafness, autosomal dominant, type 22 (DFNA-22)), OMIM:606346)

Official abbreviation DFNA22
Name deafness, autosomal dominant, type 22 (DFNA-22)
OMIM ID 606346
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 MYO6
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

2 entries on 1 page. Showing entries 1 - 2.
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00059028 - - - - no Israel Jewish-Ashkenazi - - - - DFNA22 Teen onset (12-17y), moderate-profound hearing loss - MYO6 1 3 Zippi Brownstein
00386331 186502 - - M ? - - - - - - DFNA22 Hearing impairment, Sensorineural hearing impairment, Hyperactivity, sister also affected (untested) MYO6 MYO6 1 1 Andreas Laner
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