Disease #05209 (ODA (Ocular developmental anomalies))
| Official abbreviation |
ODA |
| Name |
Ocular developmental anomalies |
| OMIM ID |
- |
| Inheritance |
- |
| Individuals reported having this disease |
7 |
| Phenotype entries for this disease |
7 |
| Associated with 1 gene |
PTCH1 |
| Associated tissues |
eyes |
| Disease features |
Anophthalmia/microphthalmia, anterior segment mesenchymal dysgenesis |
| Remarks |
- |
| Date created |
2016-12-10 11:18:31 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
|