Disease #02047 (SHEP2 (pigmentation, skin/hair/eye, variation in, type 2 (SHEP-2)), OMIM:266300)
Official abbreviation |
SHEP2 |
Name |
pigmentation, skin/hair/eye, variation in, type 2 (SHEP-2) |
OMIM ID |
266300 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
25 |
Phenotype entries for this disease |
25 |
Associated with 1 gene |
MC1R |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|