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 CCHS syndrome, hypoventilation, central, congenital (CCHS, Haddad syndrome, Ondine-Hirschsprung disease) 209880 - 99 99 ASCL1, BDNF, EDN3, GDNF, PHOX2B, RET - -
03401 HSCR-3 Hirschsprung disease, type 3 (HSCR-3) 613711 - 0 0 GDNF - -
01503 pheochromocytoma pheochromocytoma 171300 - 146 142 GDNF, KIF1B, MAX, RET, SDHB, SDHD, TMEM127, VHL - -
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