Disease #06629 (GINGF5 (fibromatosis, gingival, type 5), OMIM:617626)
| Official abbreviation |
GINGF5 |
| Name |
fibromatosis, gingival, type 5 |
| OMIM ID |
617626 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
3 |
| Associated with 1 gene |
REST |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
2023-01-05 14:47:46 +01:00 (CET) |
Individuals
|