Disease #01544 (RB1 (retinoblastoma, type 1), OMIM:180200)
| Official abbreviation |
RB1 |
| Name |
retinoblastoma, type 1 |
| OMIM ID |
180200 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant, Somatic mutation |
| Individuals reported having this disease |
67 |
| Phenotype entries for this disease |
66 |
| Associated with 1 gene |
RB1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2025-01-14 18:01:23 +01:00 (CET) |
Individuals
|