Disease #00466 (SHEP-7 (pigmentation, hair, blond/brown, type 7 (SHEP-7, skin/hair/eye pigmentation)), OMIM:611664)
| Official abbreviation |
SHEP-7 |
| Name |
pigmentation, hair, blond/brown, type 7 (SHEP-7, skin/hair/eye pigmentation) |
| OMIM ID |
611664 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
KITLG |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-07-21 17:01:43 +02:00 (CEST) |
| Date last edited |
N/A |
|
