Disease #05797 (CSS11 (Coffin-Siris syndrome, type 11 (CSS11)), OMIM:618779)
| Official abbreviation |
CSS11 |
| Name |
Coffin-Siris syndrome, type 11 (CSS11) |
| OMIM ID |
618779 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
SMARCD1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-07-25 09:07:00 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|
Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.
|