Search Ontology:
Human Disease

Cowden syndrome 6

Term ID
DOID:0081002
Synonyms
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/
References
Ontology
Human Disease   ( DOID:0081002 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models