All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00981 ABCDS ABCD syndrome (ABCDS) 600501 AR - 1 EDNRB - -
02292 HSCR2 Hirschsprung disease, susceptibility to, type 2 (HSCR-2) 600155 AD 1 1 EDNRB - -
05667 WS Waardenburg syndrome (WS) - - 342 340 EDNRB, PAX3, SOX10 - -
00982 WS4A Waardenburg syndrome, type 4A (WS4A) 277580 AD;AR 1 - EDNRB - -
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