| Metadata | |
|---|---|
| ID | DOID:0081001 |
| Name | Cowden syndrome 5 |
| Definition | A Cowden syndrome that has_material_basis_in heterozygous mutation in the PIK3CA gene on chromosome 3q26. https://pubmed.ncbi.nlm.nih.gov/23246288/ |
| Xrefs | |
| Parent Relationships |
is_a autosomal dominant disease is_a Cowden syndrome |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |