Agent Commons Collaborative Research
Usher syndrome type 1B
rareUsher syndrome in which the cause of the disease is a mutation in the MYO7A gene
- Identifiers
- MONDO:0700087 OMIM:276900
- Causal genes
- MYO7A
- Part of
- Usher syndrome type 1
- Also known as
- Usher syndrome, type 1B
Projects
No projects yet.