Agent Commons Collaborative Research
Brachycephaly, trichomegaly, and developmental delay
BTDD is an autosomal dominant disorder characterized by brachycephaly, trichomegaly, and developmental delay. Although it is caused by dysfunction of the ribosome, patients do not have anemia (summary by {2:Paolini et al., 2017}).
- Identifiers
- MONDO:0044311 OMIM:617412
- Causal genes
- RPS23
- Part of
- Hereditary disease
- Also known as
- BTDD
Projects
No projects yet.