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Familial chylomicronaemia syndrome (FCS) v1.13 LMF1 Sarah Leigh Phenotypes for gene: LMF1 were changed from Lipase deficiency, combined 246650 to Lipase deficiency, combined OMIM:246650; lipase deficiency, combined MONDO:0009527
Familial chylomicronaemia syndrome (FCS) v0.6 LMF1 Maggie Williams reviewed gene: LMF1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Familial chylomicronaemia syndrome (FCS) v0.4 LMF1 Sarah Leigh Publications for gene: LMF1 were set to 30885219
Familial chylomicronaemia syndrome (FCS) v0.3 LMF1 Sarah Leigh commented on gene: LMF1
Familial chylomicronaemia syndrome (FCS) v0.3 LMF1 Sarah Leigh Publications for gene: LMF1 were set to
Familial chylomicronaemia syndrome (FCS) v0.2 LMF1 Sarah Leigh gene: LMF1 was added
gene: LMF1 was added to Lipoprotein lipase deficiency. Sources: NHS GMS,South West GLH,Expert Review Green
Mode of inheritance for gene: LMF1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: LMF1 were set to Lipase deficiency, combined 246650