Disease #02298 (DFNB3 (deafness, autosomal recessive, type 3 (DFNB-3)), OMIM:600316)

Official abbreviation DFNB3
Name deafness, autosomal recessive, type 3 (DFNB-3)
OMIM ID 600316
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 18
Phenotype entries for this disease 18
Associated with 1 gene MYO15A
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)


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18 entries on 1 page. Showing entries 1 - 18.
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00059023 - Karen Avraham lab, Tel Aviv University, unpublished data - - yes Israel Arab - - - - DFNB3 congenital profound hearing loss - MYO15A 1 2 Zippi Brownstein
00059038 - Karen Avraham laboratory, Tel Aviv university, Israel, unpublished - - yes Israel Arab - - - - DFNB3 Congenital, profound hearing loss - MYO15A 1 2 Zippi Brownstein
00059039 - Karen Avraham laboratory, Tel Aviv university, Israel, unpublished - - yes Israel Arab - - - - DFNB3 Congenital, profound hearing loss - MYO15A 1 2 Zippi Brownstein
00059040 - Karen Avraham laboratory, Tel Aviv university, Israel, unpublished - - no Israel Jewish-Bukharian - - - - DFNB3 Congenital, profound hearing loss - MYO15A 1 2 Zippi Brownstein
00059042 - Karen Avraham laboratory, Tel Aviv university, Israel, unpublished - - yes Israel Arab - - - - DFNB3 congenital, profound hearing loss - MYO15A 1 2 Zippi Brownstein
00060233 - PubMed: Brownstein 2014, Journal: Brownstein 2014 2-generation family, 2 affected sisters, unaffected heterozygous carrier parents F yes Israel Iran;Jewish - - - - DFNB3 Congenital, profound - MYO15A 1 2 Zippi Brownstein
00060235 - PubMed: Brownstein 2011, Journal: Brownstein 2011 - - no Israel Jewish-Ashkenazi - - - - DFNB3 Congenital, profound - MYO15A 2 2 Zippi Brownstein
00081020 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - DFNB3 Deafness, autosomal recessive 3 (OMIM:600316) MYO15A MYO15A 1 1 Daniel Trujillano
00154503 - - - M yes Israel - - - - 3 DFNB3 Congenital profound hearing loss - MYO15A 1 1 Nada Danial-Farran
00428321 Fam9 PubMed: Wonkam 2022 2-generation family, 2 affected sisters, unaffected heterozygous carrier parents F no Ghana Africa - - - - DFNB3 - - MYO15A 2 2 Yacouba Dia
00428322 Fam11 PubMed: Wonkam 2022 3-generation family, 2 affected brothers, unaffected heterozygous carrier parents M no Ghana Africa - - - - DFNB3 - - MYO15A 2 2 Yacouba Dia
00428323 Fam13 PubMed: Wonkam 2022 3-generation family, affected sister/brother (F, M), unaffected heterozygous carrier mother M no Ghana Africa - - - - DFNB3 - - MYO15A 2 2 Yacouba Dia
00428326 Fam21 PubMed: Wonkam 2022 3-generation family, 2 affected sisters F no Ghana Africa - - - - DFNB3 - - MYO15A 2 2 Yacouba Dia
00428372 Fam22 PubMed: Wonkam 2022 3-generation family, 2 affected brothers (2M). Only affected individuals were screened. M no Ghana Africa - - - - DFNB3 - - MYO15A 2 2 Yacouba Dia
00428373 Fam23 PubMed: Wonkam 2022 3-generation family, 2 affected (1F, 1M), unaffected heterozygous carrier father M no Ghana Africa - - - - DFNB3 - - MYO15A 2 2 Yacouba Dia
00428378 Fam34 PubMed: Wonkam 2022 3-generation family, 2 affected brothers M no Ghana Africa - - - - DFNB3 - - MYO15A 2 2 Yacouba Dia
00428379 Fam50 PubMed: Wonkam 2022 3-generation family, 2 affected brothers M no Ghana Africa - - - - DFNB3 - - MYO15A 2 2 Yacouba Dia
00448264 - - - - yes Pakistan - - - - - DFNB3 severe hearing loss - MYO15A 1 1 Hina Khan
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