Disease #03832 (CWS6 (Cowden syndrome, type 6 (CWS-6)), OMIM:615109)
Official abbreviation |
CWS6 |
Name |
Cowden syndrome, type 6 (CWS-6) |
OMIM ID |
615109 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
AKT1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|
|