Disease #05932 (OTSC (otosclerosis (OTSC)))

Official abbreviation OTSC
Name otosclerosis (OTSC)
OMIM ID -
Inheritance Autosomal recessive
Individuals reported having this disease 7
Phenotype entries for this disease 7
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2021-05-11 17:31:37 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00372920 - PubMed: Ziff 2016 - - - - - - - - - OTSC - SERPINF1 SERPINF1 1 1 Raymond Dalgleish
00372944 - PubMed: Ziff 2016 - - - - - - - - - OTSC - SERPINF1 SERPINF1 1 1 Raymond Dalgleish
00372945 - PubMed: Ziff 2016 A subsequent study, {PMID30968248:Valgaeren et al., 2019}, demonstrates that variant detected in this patient is not pathogenic. - - - - - - - - OTSC - SERPINF1 SERPINF1 1 1 Raymond Dalgleish
00372950 - PubMed: Ziff 2016 - - - - - - - - - OTSC - SERPINF1 SERPINF1 1 1 Raymond Dalgleish
00372953 - PubMed: Ziff 2016 - - - - - - - - - OTSC - SERPINF1 SERPINF1 1 1 Raymond Dalgleish
00372954 - PubMed: Ziff 2016 - - - - - - - - - OTSC - SERPINF1 SERPINF1 1 1 Raymond Dalgleish
00372957 - PubMed: Ziff 2016 Patient ID OTSC134 corresponds to Family B. ; The reported variant in this patient lies in the 5´UTR of an alternative transcript (ENST00000573763.1) which is the major transcript in stapes bone. The substitution (c.-1G>A) results in altered expression of that transcript. - - - Europe;Caribbean - - - - OTSC - SERPINF1 SERPINF1 1 1 Raymond Dalgleish
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