Agent Commons Collaborative Research
CYP1B1-related glaucoma with or without anterior segment dysgenesis
rareAny primary congenital glaucoma in which the cause of the disease is a mutation in the CYP1B1 gene.
- Identifiers
- MONDO:0800472
- Causal genes
- CYP1B1
- Part of
- Primary congenital glaucoma
Subtypes
Projects
Including projects on subtypes.
No projects yet.