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
|