Disease #04294 (SNHL (hearing loss, sensorineural (SNHL)))

Official abbreviation SNHL
Name hearing loss, sensorineural (SNHL)
OMIM ID -
Inheritance -
Individuals reported having this disease 23
Phenotype entries for this disease 28
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2015-06-22 12:14:54 +02:00 (CEST)
Date last edited 2015-10-23 11:42:37 +02:00 (CEST)


Individuals

23 entries on 1 page. Showing entries 1 - 23.
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00029719 - PubMed: Webb 2015, Journal: Webb 2015 2-generation family, 2 affected brothers, unaffected heterozygous carrier parents M no (Netherlands) - - - - - SNHL see paper; developmental delay, poor growth, sensorineural hearing loss, ... - MARS2 2 2 Bryn Webb
00056391 - PubMed: Kose 2014, Journal: Kose 2014 - F yes Turkey - >18y - - - RTADR, SNHL see paper, extensive description, see paper; extensive description ATP6V0A4 ATP6V0A4 1 1 Johan den Dunnen
00072499 - - OMIM602690:0013; 1 family 13 affected; 2 isolated cases - - Australia; France; Spain - - - - - PGL, SNHL , SNHL Tinnitus SDHD SDHD 1 3 Jean-Pierre Bayley
00100508 - - - - - China - - - - - SNHL - - SMPX 1 1 Zhijie Niu
00207332 - - 2 patients from 2 unrelated patients - - - - - - - - SNHL - SERPINB6 SERPINB6 1 2 LOVD
00207333 - - heterozygous patient - - - - - - - - SNHL - SERPINB6 SERPINB6 1 1 LOVD
00207334 - - 3 patients from 2 unrelated patients - - - - - - - - SNHL - SERPINB6 SERPINB6 1 3 LOVD
00207335 - - heterozygous patient - - - - - - - - SNHL - SERPINB6 SERPINB6 1 1 LOVD
00207336 - - heterozygous patient - - - - - - - - SNHL - SERPINB6 SERPINB6 1 1 LOVD
00207337 - - 8 patients from 8 unrelated patients - - - - - - - - SNHL - SERPINB6 SERPINB6 1 8 LOVD
00207338 - - affected sister non-carrier - - Turkey - - - - - SNHL - SERPINB6 SERPINB6 2 1 LOVD
00207339 - - 5-generation family, 5 affecteds - yes Turkey - - - - - SNHL - SERPINB6 SERPINB6 2 5 LOVD
00388712 Fam2 PubMed: Hochbeg 2021 2-generation family, 1 affected, unaffected heterozygous carrier parents M - - - - - - - SNHL sensorineural hearing loss - KIAA0391 2 1 Johan den Dunnen
00388713 Fam3 PubMed: Hochbeg 2021 2-generation family, 1 affected, unaffected heterozygous carrier parents M - - - - - - - SNHL childhood onset sensorineural hearing loss, lactic acidosis, leukoencephalopathy - KIAA0391 2 1 Johan den Dunnen
00400060 D-7 PubMed: Austin-Tse 2018 Discovery Cohort ? - United States - - - - - SNHL sensorineural hearing loss USH2A USH2A 2 1 LOVD
00400064 R-5 PubMed: Austin-Tse 2018 Retrospective Cohort ? - United States - - - - - SNHL Progressive moderately-severe sensorineural hearing loss USH2A USH2A 2 1 LOVD
00400067 R-11 PubMed: Austin-Tse 2018 Retrospective Cohort ? - United States - - - - - SNHL Mild to moderate sensorineural hearing loss USH2A USH2A 2 1 LOVD
00400068 R-12 PubMed: Austin-Tse 2018 Retrospective Cohort ? - United States - - - - - SNHL Congenital mild to severe sensorineural hearing loss USH2A USH2A 2 1 LOVD
00400069 R-13 PubMed: Austin-Tse 2018 Retrospective Cohort ? - United States - - - - - SNHL Sloping mild to moderately-severe sensorineural hearing loss with light sensitivity USH2A USH2A 2 1 LOVD
00400070 R-14 PubMed: Austin-Tse 2018 Retrospective Cohort ? - United States - - - - - SNHL sensorineural hearing loss with a likely dominant family history of hearing loss USH2A USH2A 1 1 LOVD
00430364 - - - - no Korea, South (Republic) Asia-E - - - - SNHL ADHD CLCNKA, CLCNKB, MPZL2 CLCNKA, CLCNKB 1 1 Soyoung Lee
00448131 Family 1 - Rad et al., submitted F no Germany - - - - - HYC2, ID, SNHL , Mild intellectual disability - MPDZ 2 3 Barbara Vona
00465436 patient PubMed: Lin 2022 - F - Taiwan - - - - - SNHL see paper; ..., profound sensorineural hearing loss WFS1 WFS1 1 1 Johan den Dunnen
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