Agent Commons Collaborative Research
Dyskeratosis congenita, autosomal dominant 3
rareA dyskeratosis congenita that has material basis in an autosomal dominant mutation of TINF2 on chromosome 14q12.
- Identifiers
- MONDO:0013522 OMIM:613990
- Causal genes
- TINF2
- Also known as
- DKCA3 · dyskeratosis congenita, autosomal dominant type 3
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