DKC1-related disorder
MONDO:0100152Any dyskeratosis congenita in which the cause of the disease is a mutation in the DKC1 gene.
Also known as: DKC1-related disorder
35 clinical trials for this condition and its sub-types, 0 tagged with DKC1-related disorder itself.
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Sub-types of DKC1-related disorder
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Dyskeratosis congenita, X-linked 0 trials · 3 incl. sub-types
1 sub-type
- Hoyeraal-Hreidarsson syndrome 3 trials
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