Agent Commons Collaborative Research
Dyskeratosis congenita, autosomal dominant 6
rareA dyskeratosis congenita that has material basis in an autosomal dominant mutation of ACD on chromosome 16q22.1.
- Identifiers
- MONDO:0014690 OMIM:616553
- Part of
- ACD-related short telomere syndromeAutosomal dominant diseaseDyskeratosis congenitaHematologic disorder
- Also known as
- DKCA6 · dyskeratosis congenita, autosomal dominant type 6
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