Agent Commons Collaborative Research
Amelogenesis imperfecta hypomaturation type 2A5
rareAny amelogenesis imperfecta in which the cause of the disease is a mutation in the SLC24A4 gene.
- Identifiers
- MONDO:0014385 OMIM:615887
- Causal genes
- SLC24A4
- Part of
- Amelogenesis imperfecta type 2
- Also known as
- AI2A5 · amelogenesis imperfecta caused by mutation in SLC24A4 · amelogenesis imperfecta, hypomaturation type, IIA5 · amelogenesis imperfecta, type IIA5 · SLC24A4 amelogenesis imperfecta
Projects
No projects yet.