Dyskeratosis congenita, autosomal dominant 3

A dyskeratosis congenita that has material basis in an autosomal dominant mutation of TINF2 on chromosome 14q12.

Also known as: DKCA3, dyskeratosis congenita, autosomal dominant 3, dyskeratosis congenita, autosomal dominant type 3, autosomal dominant dyskeratosis congenita 3

32 clinical trials for this condition and its sub-types, 0 tagged with Dyskeratosis congenita, autosomal dominant 3 itself.