Disease #00947 (SHFM3 (split-hand/foot malformation, type 3, gene duplication syndrome (SHFM3)), OMIM:246560)
| Official abbreviation |
SHFM3 |
| Name |
split-hand/foot malformation, type 3, gene duplication syndrome (SHFM3) |
| OMIM ID |
246560 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
10 |
| Phenotype entries for this disease |
10 |
| Associated with 0 genes |
- |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
linked to FGF8 Cova ESHG2020 PL2.5 |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-10-18 22:36:33 +02:00 (CEST) |
Individuals
|