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Structural eye disease v1.152 GRN Arina Puzriakova Phenotypes for gene: GRN were changed from CEROID LIPOFUSCINOSIS, NEURONAL, 11, 614706; Eye Disorders to Ceroid lipofuscinosis, neuronal, 11, OMIM:614706
Structural eye disease v0.76 GRN Nicola Ragge reviewed gene: GRN: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: CEROID LIPOFUSCINOSIS, NEURONAL, 11, 614706; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Structural eye disease v0.38 GRN Ivone Leong reviewed gene: GRN: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: CEROID LIPOFUSCINOSIS, NEURONAL, 11, 614706; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Structural eye disease v0.15 GRN Ivone Leong Source NHS GMS was added to GRN.
Mode of inheritance for gene GRN was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes CEROID LIPOFUSCINOSIS, NEURONAL, 11, 614706 for gene: GRN
Structural eye disease v0.2 GRN Ellen McDonagh gene: GRN was added
gene: GRN was added to Structural eye disease. Sources: Expert Review Red
Mode of inheritance for gene: GRN was set to
Phenotypes for gene: GRN were set to Eye Disorders