Disease #07278 (SRS5 (Silver-Russell syndrome, type 5), OMIM:618908)
| Official abbreviation |
SRS5 |
| Name |
Silver-Russell syndrome, type 5 |
| OMIM ID |
618908 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
HMGA2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2026-08-05 16:16:59 +02:00 (CEST) |
| Date last edited |
N/A |
|
Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.
|