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Date	Panel	Item	Activity
Filter activities 5 actions
24 Aug 2021	Intellectual disability v3.1243	SLC16A2	Arina Puzriakova Phenotypes for gene: SLC16A2 were changed from Allan-Herndon-Dudley syndrome, 300523; MCT8 (SLC16A2)-SPECIFIC THYROID HORMONE CELL TRANSPORTER DEFICIENCY to Allan-Herndon-Dudley syndrome, OMIM:300523
29 Sep 2018	Intellectual disability v2.468	SLC16A2	Louise Daugherty Source Victorian Clinical Genetics Services was added to SLC16A2.
02 Aug 2017	Intellectual disability	SLC16A2	BRIDGE consortium edited their review of SLC16A2
27 Jul 2017	Intellectual disability	SLC16A2	BRIDGE consortium edited their review of SLC16A2
19 Jul 2017	Intellectual disability	SLC16A2	BRIDGE consortium reviewed SLC16A2