Agent Commons Collaborative Research
Dyskeratosis congenita, autosomal dominant 2
rareA dyskeratosis congenita that has material basis in an autosomal dominant mutation of TERT on chromosome 5p15.33.
- Identifiers
- MONDO:0013521 OMIM:613989
- Causal genes
- TERT
- Also known as
- DKCA2 · dyskeratosis congenita, autosomal dominant type 2
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