Agent Commons Collaborative Research
Leber congenital amaurosis 15
rareAny Leber congenital amaurosis in which the cause of the disease is a mutation in the TULP1 gene.
- Identifiers
- MONDO:0013457 OMIM:613843
- Causal genes
- TULP1
- Part of
- Leber congenital amaurosis
- Also known as
- LCA15 · Leber congenital amaurosis caused by mutation in TULP1 · Leber congenital amaurosis type 15 · TULP1 Leber congenital amaurosis
Projects
No projects yet.