Disease #03244 (DFNB77 (deafness, autosomal recessive, type 77 (DFNB77)), OMIM:613079)

Official abbreviation DFNB77
Name deafness, autosomal recessive, type 77 (DFNB77)
OMIM ID 613079
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 LOXHD1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-11-10 09:17:11 +01:00 (CET)


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00059048 - Karen Avraham laboratory, Tel Aviv university, Israel, unpublished - - yes Israel Arab - - - - DFNB77 congenital, profound HL - LOXHD1 1 2 Zippi Brownstein
00059049 - Karen Avraham laboratory, Tel Aviv university, Israel, unpublished - - no Israel AJ - - - - DFNB77 congenital, profound NSHL - LOXHD1 2 2 Zippi Brownstein
00163776 - - - M - - Middle Eastern - - - - DFNB77 - - LOXHD1 1 1 Nada Danial-Farran
00288340 - PubMed: Atik.T 2015 - F yes Turkey - - - - - DFNB77 Severe to profound hearing loss Non syndromic - - - 1 Luke Mansard
00428678 Fam38 PubMed: Wonkam 2022 3-generation family, 2 affected (1F,1M) F no Ghana Africa - - - - DFNB77 - - LOXHD1 2 2 Yacouba Dia
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