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Dyskeratosis congenita, autosomal recessive 6

MONDO:0014600

Any dyskeratosis congenita in which the cause of the disease is a mutation in the PARN gene.

Also known as: DKCB6, PARN dyskeratosis congenita, dyskeratosis congenita caused by mutation in PARN, dyskeratosis congenita, autosomal recessive 6, dyskeratosis congenita, autosomal recessive type 6, autosomal recessive dyskeratosis congenita 6

32 clinical trials for this condition and its sub-types, 0 tagged with Dyskeratosis congenita, autosomal recessive 6 itself.

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