All individuals with variants in gene EDN3

29 entries on 1 page. Showing entries 1 - 29.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

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Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00285365 - PubMed: Sangkhathat 2006 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00285366 - PubMed: Garcia-Barceló 2004 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00285368 - PubMed: Svensson 1999 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00285376 - PubMed: Miller 2010, PubMed: Farwell 2015 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00285378 - PubMed: Sangkhathat 2006 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00285379 - PubMed: Xiong 2015 - - - - - - - - - WS Hirschsprung disease 1 1 Global Variome, with Curator vacancy
00285380 - PubMed: Sangkhathat 2006 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00285381 - PubMed: Miyagawa 2013 - - - - - - - - - deafness - 1 1 Global Variome, with Curator vacancy
00315505 - PubMed: Bidaud 1997, PubMed: Garcia-Barcelo 2004 - - - - - - - - - HSCR - 1 1 Veronique Pingault
00315506 - PubMed: Bidaud 1997, PubMed: Bidaud 1997 - M yes - - - - - - WS - 1 2 Veronique Pingault
00315507 - PubMed: Edery 1996, PubMed: Bidaud 1997 - F no - - - - - - WS - 1 2 Veronique Pingault
00315508 - PubMed: Pingault 2010 - M no Bosnia and Herzegovina Bosnia - - - - WS - 1 1 Veronique Pingault
00315509 - PubMed: Pingault 2010 - F no - - - - - - WS - 1 1 Veronique Pingault
00315510 - PubMed: Pingault 2010 - M yes India;Madagascar Caribbean - - - - WS - 1 1 Veronique Pingault
00315511 - PubMed: Pingault 2010 - M yes India - - - - - WS depigmentations in heterozygous relatives 1 1 Veronique Pingault
00315512 - PubMed: Pingault 2010 - F - India - - - - - WS - 2 1 Veronique Pingault
00315513 - PubMed: Vinuela 2009 - M yes - - - - - - WS depigmentation, deafness in heterozygous relatives 1 1 Veronique Pingault
00315514 - PubMed: Pingault 2002 - M - India - - - - - WS depigmentation, deafness in heterozygous relatives 1 1 Veronique Pingault
00315515 - PubMed: Hofstra 1996 - - yes Pakistan - - - - - WS depigmentation in heterozygous relatives 1 1 Veronique Pingault
00315516 - PubMed: Pingault 2010 - - yes Pakistan - - - - - WS - 1 1 Veronique Pingault
00315517 - PubMed: Pingault 2010 - - yes Pakistan - - - - - WS - 1 1 Veronique Pingault
00315518 - PubMed: Pingault 2001 - F - Yugoslavia - - - - - WS - 1 1 Veronique Pingault
00315519 - PubMed: Bolk 1996 - - - - - - - - - CDHS - 1 1 Veronique Pingault
00315520 - PubMed: Bidaud 1997 - - - - - - - - - HSCR - 1 1 Veronique Pingault
00315521 - PubMed: Shamseldin 2010 - M - Egypt - - - - - WS hypoplastic ears. Consanguineous family 1 1 Veronique Pingault
00315522 - PubMed: Kapoor 2012 patient also has Duchenne muscular dystrophy, homozygote brother has WS4 M yes India - - - - - WS - 1 1 Veronique Pingault
00315557 FamPatII5 PubMed: Cui 2013 3-generation family, 5 affected (2F, 3M), mixed phenotypes M - Brazil European - - - - HSCR see paper; ..., Hirschsprung disease, heterochromia iridum 1 5 Veronique Pingault
00428017 A158 PubMed: Bournazos 2022 family, 1 affected - - Australia - - - - - ? - 1 1 Johan den Dunnen
00468843 - PubMed: Retterer 2016 analysis proband (1/3040) - - United States - - - - - ? developmental dealy, short stature, hearing loss, brachydactyly 1 1 Johan den Dunnen
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