Disease #05986 (ODLURO (O'Donnell-Luria-Rodan syndrome), OMIM:618512)
| Official abbreviation |
ODLURO |
| Name |
O'Donnell-Luria-Rodan syndrome |
| OMIM ID |
618512 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
MLL5 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-11-08 09:24:31 +01:00 (CET) |
| Date last edited |
2022-06-28 19:36:48 +02:00 (CEST) |
Individuals
|