All diseases

1 entry on 1 page. Showing entry 1.
Legend   How to query  

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 - -
Legend   How to query