All diseases

5 entries on 1 page. Showing entries 1 - 5.
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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 - -
02668 BULN-1 bulimia nervosa, susceptibility to, type 1 (BULN-1) 607499 - - - BDNF - -
02925 BULN-2 bulimia nervosa, susceptibility to, type 2 (BULN-2) 610269 - - - BDNF - -
00292 OCD obsessive compulsive disorder (OCD) 164230 - - - BDNF, HTR2A, SLC6A4 - -
00953 WAGRO Wilms tumor, aniridia, genitourinary anomalies, mental retardation, and obesity syndrome (WAGRO) - - - - BDNF, PAX6, WT1 - -
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