Disease #00420 (STGD-1 (Stargardt disease, type 1 (STGD-1)), OMIM:248200)
| Official abbreviation |
STGD-1 |
| Name |
Stargardt disease, type 1 (STGD-1) |
| OMIM ID |
248200 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 2 genes |
ABCA4, CNGB3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-06-16 23:00:12 +02:00 (CEST) |
| Date last edited |
N/A |
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