All diseases

5 entries on 1 page. Showing entries 1 - 5.
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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 - -
02985 HPE7 holoprosencephaly, type 7 (HPE-7) 610828 AD 7 7 PTCH1 - -
05150 KCOT tumor, keratocystic odontogenic (KCOT) - - 17 17 PTCH1 - -
05209 ODA Ocular developmental anomalies - - 7 7 PTCH1 eyes Anophthalmia/microphthalmia, anterior segment mesenchymal dysgenesis
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