Disease #04581 (WNCHRS (Winchester? syndrome (WNCHRS)), OMIM:277950)
| Official abbreviation |
WNCHRS |
| Name |
Winchester? syndrome (WNCHRS) |
| OMIM ID |
277950 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
MMP14 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:23 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|