Allan-Herndon-Dudley syndrome

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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: ALLAN-HERNDON SYNDROME, AHDS

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

MIM:

MIM:300523 - allan-herndon-dudley syndrome; ahds

MIM:300523 - allan-herndon-dudley syndrome; ahds

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), X-linked recessive disease (is_a)