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31 Aug 2021	Intellectual disability - microarray and sequencing v3.1246	SLC25A15	Arina Puzriakova Phenotypes for gene: SLC25A15 were changed from Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome, 238970 -3; HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME (HHH SYNDROME) to Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome, OMIM:238970
29 Sep 2018	Intellectual disability - microarray and sequencing v2.468	SLC25A15	Louise Daugherty Source Victorian Clinical Genetics Services was added to SLC25A15.
02 Aug 2017	Intellectual disability - microarray and sequencing	SLC25A15	BRIDGE consortium edited their review of SLC25A15
27 Jul 2017	Intellectual disability - microarray and sequencing	SLC25A15	BRIDGE consortium edited their review of SLC25A15
19 Jul 2017	Intellectual disability - microarray and sequencing	SLC25A15	BRIDGE consortium reviewed SLC25A15