Disease #05602 (SHFLD3 (split-hand/foot malformation with long bone deficiency, type 3 (SHFLD-3, Gollop-Wolfgang complex (GWC))), OMIM:612576)
| Official abbreviation |
SHFLD3 |
| Name |
split-hand/foot malformation with long bone deficiency, type 3 (SHFLD-3, Gollop-Wolfgang complex (GWC)) |
| OMIM ID |
612576 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
11 |
| Phenotype entries for this disease |
11 |
| Associated with 1 gene |
BHLHA9 |
| Associated tissues |
- |
| Disease features |
autosomal recessive |
| Remarks |
- |
| Date created |
2019-05-24 15:53:26 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|