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
02551 BCC-1 carcinoma, basal cell, susceptibility to, type 1 (BCC-1) 605462 - - - PTCH1, PTCH2, RASA1 - -
01191 BCNS basal cell nevus syndrome (BCNS, Gorlin-Goltz syndrome) 109400 - - - PTCH1, PTCH2, SUFU - -
02985 HPE-7 holoprosencephaly, type 7 (HPE-7) 610828 - - - PTCH1 - -
05150 KCOT tumor, keratocystic odontogenic (KCOT) - - - - PTCH1 - -
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