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DOID:0081002 - Cowden syndrome 6
Disease Ontology Definition:A Cowden syndrome that has_material_basis_in heterozygous mutation in the AKT1 gene on chromosome 14q32.3.
Synonyms:
Xenbase Genes : akt1
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Cowden syndrome (is_a)