Disease #05794 (CSS7 (Coffin-Siris syndrome, type 7 (CSS7)), OMIM:618027)
| Official abbreviation |
CSS7 |
| Name |
Coffin-Siris syndrome, type 7 (CSS7) |
| OMIM ID |
618027 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
DPF2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-07-25 09:00:44 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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