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
| Disease | Subtypes |
|---|---|
| Anterior segment dysgenesis 6 | |
| Glaucoma 3A |
Rare disease
Projects
Including projects on subtypes.
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