Dyskeratosis congenita, autosomal recessive 2

MONDO:0013519

A dyskeratosis congenita that has material basis in an autosomal recessive mutation of NOLA2 on chromosome 5q35.3.

Also known as: DKCB2, dyskeratosis congenita, autosomal recessive 2, dyskeratosis congenita, autosomal recessive type 2, autosomal recessive dyskeratosis congenita 2

43 clinical trials for this condition and its sub-types.

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