All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00900 - Central hypoventilation syndrome, congenital, with or without Hirschsprung disease (Haddad syndrome) 209880 - - - ASCL1, BDNF, EDN3, GDNF, PHOX2B, RET - -
03402 HSCR-4 Hirschsprung disease, type 4 (HSCR-4) 613712 - - - EDN3 - -
03295 WS-4B Waardenburg syndrome, type 4B (WS-4B) 613265 - - - EDN3 - -
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