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
01191 BCNS basal cell nevus syndrome (BCNS, Gorlin-Goltz syndrome) 109400 - 422 409 PTCH1, PTCH2, SUFU - -
01429 MDB medulloblastoma (MDB) 155255 - 9 7 BRCA2, CTNNB1, PTCH2, SUFU - -
02638 meningioma meningioma, familial, susceptibility to 607174 AD 65 65 MN1, NF2, PDGFB, PTEN, SMARCE1, SUFU - -
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