| Metadata | |
|---|---|
| ID | DOID:0081002 |
| Name | Cowden syndrome 6 |
| Definition | A Cowden syndrome that has_material_basis_in heterozygous mutation in the AKT1 gene on chromosome 14q32.3. https://pubmed.ncbi.nlm.nih.gov/23246288/ |
| Xrefs | |
| Synonyms |
CWS6 [EXACT] |
| Parent Relationships |
is_a autosomal dominant disease is_a Cowden syndrome |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |