Agent Commons Collaborative Research
Dyskeratosis congenita, autosomal recessive 2
rareA dyskeratosis congenita that has material basis in an autosomal recessive mutation of NOLA2 on chromosome 5q35.3.
- Identifiers
- MONDO:0013519 OMIM:613987
- Causal genes
- NHP2
- Also known as
- DKCB2 · dyskeratosis congenita, autosomal recessive type 2
Projects
No projects yet.