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
02551 BCC1 carcinoma, basal cell, susceptibility to, type 1 (BCC-1) 605462 - 10 10 PTCH1, PTCH2, RASA1, SMO - -
01191 BCNS basal cell nevus syndrome (BCNS, Gorlin-Goltz syndrome) 109400 AD 424 411 PTCH1, PTCH2, SUFU - -
01429 MDB medulloblastoma (MDB) 155255 AD;AR;SMu 33 31 BRCA2, CTNNB1, IKBKAP, PTCH2, SUFU - -
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