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 CCHS hypoventilation, central, syndrome, congenital, with/without Hirschsprung disease (CCHS1) 209880 AD 100 99 PHOX2B - -
00901 NBLST2 neuroblastoma, susceptibility to, type 2 (NBLST-2) 613013 - - - PHOX2B - -
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