Disease #04622 (DFNX2 (deafness, X-linked, type 2 (DFNX-2)), OMIM:304400)

Official abbreviation DFNX2
Name deafness, X-linked, type 2 (DFNX-2)
OMIM ID 304400
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene POU3F4
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +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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00060263 - PubMed: Parzefall 2013, Journal: Parzefall 2013 Congenital, profound HL; Mondini M no Israel Jewish-Ashkenazi - - - - DFNX2 - - POU3F4 1 1 Zippi Brownstein
00114821 - - - M no Israel Jewish-Ashkenazi - - - - DFNX2 DFNX2; Hearing_loss POU3F4 POU3F4 1 1 Thomas Parzefall
00114822 - - - M no Israel Jewish-Ashkenazi - - - - DFNX2 DFNX2; Hearing_loss POU3F4 POU3F4 1 1 Thomas Parzefall
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