All individuals with variants in gene AUH

18 entries on 1 page. Showing entries 1 - 18.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00001766 - Submitted by J. Zschocke - M ? - - - - - - EDS ascertainment ; clinical presentation 2 1 Division of Human Genetics, Innsbruck
00001767 - Submitted by J. Zschocke - F ? - - - - - - EDS ascertainment ; clinical presentation 2 1 Division of Human Genetics, Innsbruck
00001768 - PubMed: Ensenauer 2000, Patient 1 in PubMed: IJlst 2002, Patient 6 in PubMed: Wortmann 2010 - M ? Afghanistan - - - - - EDS ascertainment ; clinical presentation 2 1 Division of Human Genetics, Innsbruck
00001769 - Patient 2 in PubMed: IJlst 2002, Patient 3 in PubMed: Ly 2003, Patient 10 in PubMed: Wortmann 2010 sibling of patient 9 in Wortmann et al. (2010) = patient 2 in Ly et al. (2003) M ? Morocco - - - - - EDS ascertainment ; family analysis 2 1 Division of Human Genetics, Innsbruck
00001770 - Patient 1 in PubMed: Ly 2003, Patient 4 in PubMed: Wortmann 2010 - M ? Lebanon - - - - - EDS ascertainment ; newborn screening 2 1 Division of Human Genetics, Innsbruck
00001771 - PubMed: Ensenauer 2000, PubMed: Ly 2003 - M ? Afghanistan - - - - - EDS ascertainment ; clinical presentation 2 1 Division of Human Genetics, Innsbruck
00001772 - Patient 5 in PubMed: Ly 2003, PubMed: Gibson 1998, PubMed: Jooste 1994, Patient 7 in PubMed: Wortmann 2010 - F ? - - - - - - EDS ascertainment ; clinical presentation 2 1 Division of Human Genetics, Innsbruck
00001773 - PubMed: Illsinger 2004, Patient 8 in PubMed: Wortmann 2010 - M ? Germany white - - - - EDS ascertainment ; clinical presentation 2 1 Division of Human Genetics, Innsbruck
00001774 - PubMed: Shoji 1999, PubMed: Matsumori 2005, Patient 5 in PubMed: Wortmann 2010 - M ? Japan - - - - - EDS ascertainment ; clinical presentation 2 1 Division of Human Genetics, Innsbruck
00001775 - Patient 1 in PubMed: Wortmann 2010, PubMed: Engelke 2006 - F ? Netherlands - - - - - EDS ascertainment ; clinical presentation; optic atrophy, ataxia, spasticity 2 1 Division of Human Genetics, Innsbruck
00001776 - Patient 2 in PubMed: Wortmann 2010 - M yes United Kingdom (Great Britain) - - - - - EDS ascertainment ; clinical presentation; dementia, ataxia, spasticity, cerebellar syndrome 2 1 Division of Human Genetics, Innsbruck
00001777 - Patient 2 in PubMed: Ly 2003, Patient 9 in PubMed: Wortmann 2010 sibling of patient 2 in Ijlst et al. (2002) = patient 3 in Ly et al. (2003) = patient 10 in Wortmann et al. (2010) M ? Morocco - - - - - EDS - 2 1 Division of Human Genetics, Innsbruck
00001778 - PubMed: Eriguchi 2006, Patient 3 in PubMed: Wortmann 2010 - F yes - - - - - - EDS ascertainment ; clinical presentation; dementia, ataxia 2 1 Division of Human Genetics, Innsbruck
00294887 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00294888 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 257 Mohammed Faruq
00294889 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 29 Mohammed Faruq
00305254 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 8 Mohammed Faruq
00374222 S-2049 PubMed: Ganapathy 2019 - - - India - - - - - ? Slurring of speech and multifocal dystonia 1 1 Johan den Dunnen
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.