Disease #04512 (SRS3;GRDF (Silver-Russell syndrome, type 3), OMIM:616489)
| Official abbreviation |
SRS3;GRDF |
| Name |
Silver-Russell syndrome, type 3 |
| OMIM ID |
616489 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
IGF2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
| Date last edited |
2026-08-05 16:18:48 +02:00 (CEST) |
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