| Metadata | |
|---|---|
| ID | DOID:0081003 |
| Name | Cowden syndrome 7 |
| Definition | A Cowden syndrome that has_material_basis_in heterozygous mutation in the SEC23B gene on chromosome 20p11. https://pubmed.ncbi.nlm.nih.gov/26522472/ |
| Xrefs | |
| Parent Relationships |
is_a autosomal dominant disease is_a Cowden syndrome |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |