Dyskeratosis congenita, autosomal dominant 1
MONDO:0007485A dyskeratosis congenita that has material basis in an autosomal dominant mutation of TERC on chromosome 3q26.2.
Also known as: DKCA1, dyskeratosis congenita, Scoggins type, dyskeratosis congenita, autosomal dominant 1, dyskeratosis congenita, autosomal dominant type 1, DKCA, autosomal dominant dyskeratosis congenita, autosomal dominant dyskeratosis congenita 1, dyskeratosis congenita Scoggins type
34 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
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New online tool aims to help families uncover hidden cancer risks
Knowledge-focused Not yet recruitingThis study tests whether a new online program can help families understand their inherited cancer risk and encourage relatives to get low-cost genetic testing. Researchers will enroll 400 adults who carry a cancer-related gene change and their family members. The goal is to see i…
Phase: NA • Sponsor: Stanford University • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:33 UTC
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50,000 samples to unlock secrets of hereditary tumors
Knowledge-focused Not yet recruitingThis study will collect blood and tumor tissue from up to 50,000 adults with hereditary or genetic-linked cancers. Researchers will use these samples to create lab-grown tumor models, like mini-tumors, to study how these cancers work and test new treatments. The goal is to better…
Sponsor: University of California, San Francisco • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:28 UTC