Disease #00651
Official abbreviation |
608902 |
Name |
Disorder due cytochrome p450 CYP2D6 variant |
OMIM ID |
608902 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 0 genes |
- |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|