Disease #02466 (DFNB16 (deafness, autosomal recessive, type 16 (DFNB-16)), OMIM:603720)

Official abbreviation DFNB16
Name deafness, autosomal recessive, type 16 (DFNB-16)
OMIM ID 603720
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene STRC
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

5 entries on 1 page. Showing entries 1 - 5.
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00060269 - PubMed: Francey 2012, Journal: Francey 2012 - - no Israel Jewish-Ashkenazi - - - - DFNB16 Congenital, mild-moderate NSHL - STRC 2 3 Zippi Brownstein
00060271 - - - - no Israel Jewish-Ashkenazi - - - - DFNB16 Congenital, mild-moderate NSHL - STRC 2 1 Zippi Brownstein
00060273 - Karen Avraham Laboratory - - no Israel Jewish-Ashkenazi - - - - DFNB16 Congenital, moderate NSHL - STRC 1 2 Zippi Brownstein
00060274 - Karen Avraham Laboratory - - no Israel Jewish-Ashkenazi - - - - DFNB16 Congenital, mild-moderate NSHL - STRC 2 1 Zippi Brownstein
00173910 Family STRC: Ind. III:6 - - M no Norway - - - - - DFNB16 - - STRC 2 3 Joakim Klar
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