Disease #03182 (LCA13;RP53 (Leber congenital amaurosis, type 13 (LCA13, retinitis pigmentosa, type 53 (RP53))), OMIM:612712)
| Official abbreviation |
LCA13;RP53 |
| Name |
Leber congenital amaurosis, type 13 (LCA13, retinitis pigmentosa, type 53 (RP53)) |
| OMIM ID |
612712 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant, Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
RDH12 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|