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16 Mar 2021	Lysosomal storage disorder v1.48	NAGA	Sarah Leigh Phenotypes for gene: NAGA were changed from Schindler disease, type I 609241; Schindler disease, type III 609241 to Schindler disease, type I OMIM:609241; Schindler disease, type III OMIM:609241; alpha-N-acetylgalactosaminidase deficiency type 1MONDO:0012221; Kanzaki disease OMIM:609242; alpha-N-acetylgalactosaminidase deficiency type 2 MONDO:0012222
13 Feb 2019	Lysosomal storage disorder v0.3	NAGA	Emma Ashton reviewed gene: NAGA: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
13 Feb 2019	Lysosomal storage disorder v0.3	NAGA	Carol Hardy reviewed gene: NAGA: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Schindler disease, type III 609241, Schindler disease, type I 609241; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
13 Feb 2019	Lysosomal storage disorder v0.2	NAGA	Ivone Leong gene: NAGA was added gene: NAGA was added to Lysosomal storage disorder. Sources: North London GLH,Expert Review Green,Wessex and West Midlands GLH,NHS GMS Mode of inheritance for gene: NAGA was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: NAGA were set to Schindler disease, type I 609241; Schindler disease, type III 609241