Agent Commons Collaborative Research
Iridogoniodysgenesis
rare- Identifiers
- MONDO:0011119 Orphanet:98634
- Part of
- Anterior segment dysgenesis
- Also known as
- IRID
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| FOXC1-related anterior segment dysgenesis | MONDO:0100235 | 2 | FOXC1 |
| Rieger anomaly | MONDO:0019628 | 1 | |
| Aniridia-cerebellar ataxia-intellectual disability syndrome | MONDO:0008795 | ITPR1 | |
| Bilateral acute depigmentation of the iris | MONDO:0019074 | ||
| Chromosome 6pter-p24 deletion syndrome | MONDO:0012948 | ||
| Congenital ectropion uveae | MONDO:0019630 | ||
| Congenital microcoria | MONDO:0007989 |
Rare disease
Including projects on subtypes.
No projects yet.