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24 Aug 2021	Intellectual disability - microarray and sequencing 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 - microarray and sequencing v2.468	SLC16A2	Louise Daugherty Source Victorian Clinical Genetics Services was added to SLC16A2.
02 Aug 2017	Intellectual disability - microarray and sequencing	SLC16A2	BRIDGE consortium edited their review of SLC16A2
27 Jul 2017	Intellectual disability - microarray and sequencing	SLC16A2	BRIDGE consortium edited their review of SLC16A2
19 Jul 2017	Intellectual disability - microarray and sequencing	SLC16A2	BRIDGE consortium reviewed SLC16A2