Disease #06877 (DFNA (deafness, nonsyndromic (DFNA, autosomal dominant)))

Official abbreviation DFNA
Name deafness, nonsyndromic (DFNA, autosomal dominant)
OMIM ID -
Inheritance -
Individuals reported having this disease 20
Phenotype entries for this disease 8
Associated with 6 genes GREB1L, MYO6, MYO7A, REST, TECTA, TMC1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

20 entries on 1 page. Showing entries 1 - 20.
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00132291 FamPatIV2 PubMed: Eisenberger 2018 4-generation family, 8 affected (4F, 4M) M no Germany white - - - - DFNA see paper; ... PTPRQ COL9A3, GJB2, GJB3, KCNE1, LOXHD1, LRRIQ1, MYH7B, MYO15A, PNKP, PTPRQ, RDX, SYT1, TMTC2, TSPEAR, USH2A 18 8 Hanno Bolz
00327036 SH324-721 PubMed: Kim 2022, Journal: Kim 2022 - - - Korea, South (Republic) - - - - - DFNA - - PTPN11 2 1 So Young Kim
00327080 SH321-718 PubMed: Kim 2022, Journal: Kim 2022 - - - Korea, South (Republic) - - - - - DFNA - - PTPN11 1 1 So Young Kim
00327089 SB121-213 PubMed: Kim 2022, Journal: Kim 2022 - - - Korea, South (Republic) - - - - - DFNA - - USH2A 2 1 So Young Kim
00327100 SH323-720 PubMed: Kim 2022, Journal: Kim 2022 - - - Korea, South (Republic) - - - - - DFNA - - PTPN11 1 1 So Young Kim
00327102 SB356-697 PubMed: Kim 2022, Journal: Kim 2022 - - - Korea, South (Republic) - - - - - DFNA - - KCNQ4 1 1 So Young Kim
00396825 FR01242660041 Vaché et al., submitted - F no France - - - - - DFNA, DFNA5 - DFNA5 - - 1 David Baux
00396953 FR01242660041/FamS2426 PubMed: Mansard 2022 5-generation family, 16 affected (13F, 3M) F no France - - - - - DFNA, DFNA5 - DFNA5 DFNA5 1 16 David Baux
00411547 SU340 Vaché et al., submitted daughter of SU333 F no France Sicilia - - - - DFNA - - HOMER2 1 1 Anne-Françoise Roux
00411548 SU333 Vaché submitted daughter of SU332, mother of SU340 F no France Sicilia - - - - DFNA - - HOMER2, OTOF 2 1 Anne-Françoise Roux
00411549 SU332 Vaché et al., submitted 3-generation family, mother of SU333, sister of SU561 F no France Sicilia - - - - DFNA - - HOMER2, USH1C 2 6 Anne-Françoise Roux
00411550 SU561 Vaché et al., submitted brother of SU332 M no France Sicilia - - - - DFNA - - HOMER2, USH1C 2 1 Anne-Françoise Roux
00411551 SU334 Vaché submitted daughter of SU332, mother of SU7517 F no France Sicilia - - - - DFNA - - HOMER2, OTOF, USH1C 3 1 Anne-Françoise Roux
00411552 SU7517 Vaché submitted daughter of SU334 F no France Sicilia - - - - DFNA - - HOMER2, OTOF 2 1 Anne-Françoise Roux
00428310 FamPatIV3 PubMed: Manyisa 2021 4-generation family, 2 affected, mother/son, (F, M), 2 unaffected (half sister and maternal grandmother) M no South Africa Africa >12y - - - DFNA 3y-hearing impairment, progressive REST REST 1 2 Yacouba Dia
00428311 FamPatIII8 PubMed: Adadey 2022 3-generation family, 1 affected (1M), 15 unaffected (8F, 7M), three individuals screened (proband, mother, brother) M no Ghana Africa - - - - DFNA profound bilateral, symmetrical sensorineural hearing impairment (HP:0000365); no enal tubular dysfunction (-HP:0000124) GREB1L GREB1L 1 1 Yacouba Dia
00428665 FamLMG2 PubMed: Peters 2008, PubMed: Nakano 2018 2-generation family, 12 affected (6F, 6M) F;M no United States - - - - - DFNA see paper; ..., progressive, non-syndromic, sensorineural hearing loss REST REST 1 12 Johan den Dunnen
00435034 DFNA33_Affected PubMed: Bonsch 2009 4-generation family, 8 affected (3F, 5M) F;M no Germany - - - - - DFNA - - ATP11A 1 8 Barbara Vona
00441462 family PubMed: Ozieblo 2019 5-generation family, 13 affected (5F, 8M) F;M - Poland - - - - - DFNA see paper; ... - PTPRQ, TMC1 2 13 Johan den Dunnen
00448506 HLMS15 PubMed: Khan 2024, Journal: Khan 2024 - M yes Pakistan - - - - - DFNA - EYA1 EYA1 1 1 Hina Khan
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