All diseases

2 entries on 1 page. Showing entries 1 - 2.
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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 - -
00901 NBLST-2 neuroblastoma, susceptibility to, type 2 (NBLST-2) 613013 - - - PHOX2B - -
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