Dyskeratosis congenita, autosomal dominant 1

MONDO:0007485

A 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, 0 tagged with Dyskeratosis congenita, autosomal dominant 1 itself.

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↑ Telomere syndrome (92) ↑ Dyskeratosis congenita (12)

Including sub-types (34) Tagged with Dyskeratosis congenita, autosomal dominant 1 (0)

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