Disease #00476 (SHEP3 (pigmentation, eye, blue/green - skin, light/dark/freckling, type 3 (SHEP-3, skin/hair/eye pigmentation)), OMIM:601800)
| Official abbreviation |
SHEP3 |
| Name |
pigmentation, eye, blue/green - skin, light/dark/freckling, type 3 (SHEP-3, skin/hair/eye pigmentation) |
| OMIM ID |
601800 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
TYR |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-07-24 21:43:22 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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