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Summary Literature (0)
DOID:0050631 - Allan-Herndon-Dudley syndrome

Disease Ontology Definition:A syndrome that has_material_basis_in mutation in the MCT8 gene on chromosome Xq13.

Synonyms: AHDS, ALLAN-HERNDON SYNDROME

Xenbase Genes : slc16a2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010354 - Allan-Herndon-Dudley syndrome


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): syndrome (is_a), X-linked monogenic disease (is_a)