All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00115 BCNS Basal cell nevus syndrome 109400 - 0 0 PTCH1, SUFU - -
00120 FMNG Meningioma, familial, susceptibility to 607174 - 0 0 PTEN, SUFU - -
00149 JBTS32 Joubert syndrome 32 617757 - 0 0 SUFU - -
00016 MDB Medulloblastoma 155255 - 5 5 BRCA2, SUFU - -
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