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Gorlin Syndrome — Gene Therapy & Clinical Trials | FollowGene

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Home/Diseases/Gorlin Syndrome

Gorlin Syndrome

Prevalence: 1/60000

oncologic

Official·OMIM:109400 Official·ORPHA377

Basal cell carcinoma predisposition due to PTCH1 gene mutations.

Associated Genes

Chromosome 9Autosomal Dominant

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