Disease #02398 (DFNB15 (deafness, autosomal recessive, type 15 (DFNB-15)), OMIM:601869)

Official abbreviation DFNB15
Name deafness, autosomal recessive, type 15 (DFNB-15)
OMIM ID 601869
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene GIPC3
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

4 entries on 1 page. Showing entries 1 - 4.
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00080854 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - DFNB15 Deafness, autosomal recessive 15 (OMIM:601869) GIPC3 GIPC3 1 1 Daniel Trujillano
00428400 Fam10 PubMed: Wonkam 2022 3 generation family, 2 affected sisters F no Ghana Africa - - - - DFNB15 - - GIPC3 1 2 Yacouba Dia
00428401 Fam30 PubMed: Wonkam 2022 3-generation family, 3 affected (2F, 1M) F no Ghana Africa - - - - DFNB15 - - GIPC3 1 3 Yacouba Dia
00428402 Fam31 PubMed: Wonkam 2022 3-generation family, 2 affected (1M, 1F), unaffected carrier mother, unaffected homozygous sister M no Ghana Africa - - - - DFNB15 - - GIPC3 1 2 Yacouba Dia
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