Disease #00297 (GCPS (cephalopolysyndactyly, Greig syndrome (GCPS)), OMIM:175700)
| Official abbreviation |
GCPS |
| Name |
cephalopolysyndactyly, Greig syndrome (GCPS) |
| OMIM ID |
175700 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
GLI3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-01-17 17:17:13 +01:00 (CET) |
| Date last edited |
N/A |
|