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
00106 CCHS Central hypoventilation syndrome 209880 - 0 0 PHOX2B, RET - -
00107 NBLST2 Neuroblastoma, susceptibility to, 2 613013 - 0 0 PHOX2B - -
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