Disease #05863 (HSCR (Hirschsprung disease (HSCR)))

Official abbreviation HSCR
Name Hirschsprung disease (HSCR)
OMIM ID -
Inheritance -
Individuals reported having this disease 8
Phenotype entries for this disease 7
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2020-10-26 17:45:34 +01:00 (CET)
Date last edited N/A


Individuals

8 entries on 1 page. Showing entries 1 - 8.
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00315505 - PubMed: Bidaud 1997, PubMed: Garcia-Barcelo 2004 - - - - - - - - - HSCR - EDN3 EDN3 1 1 Veronique Pingault
00315520 - PubMed: Bidaud 1997 - - - - - - - - - HSCR - EDN3 EDN3 1 1 Veronique Pingault
00315527 - PubMed: Zaahl 2003 - - - China - - - - - HSCR - EDNRB EDNRB 1 1 Veronique Pingault
00315533 - PubMed: Garcia-Barcelo 2004 - - - China - - - - - HSCR - EDNRB EDNRB 1 1 Veronique Pingault
00315547 - PubMed: Auricchio 1996 - - - Italy - - - - - HSCR - EDNRB EDNRB 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 EDNRB EDN3, EDNRB 2 5 Veronique Pingault
00315814 - PubMed: Sanchez-Meijas 2010 - M - - - - - - - HSCR - SOX10 SOX10 1 1 Veronique Pingault
00466028 - - - - - - - - - - - HSCR - EDN3, EDNRB, RET RET 1 1 Gemeinschaftspraxis für Humangenetik Dresden
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