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Neurodegenerative disorders, adult onset v2.35 AARS Arina Puzriakova Phenotypes for gene: AARS were changed from to Charcot-Marie-Tooth disease, axonal, type 2N, OMIM:613287; Charcot-Marie-Tooth disease axonal type 2N, MONDO:0013212
Neurodegenerative disorders, adult onset v1.102 AARS Louise Daugherty Tag new-gene-name tag was added to gene: AARS.
Neurodegenerative disorders, adult onset v1.102 AARS Louise Daugherty commented on gene: AARS: Added new-gene-name tag, new approved HGNC gene symbol for AARS is AARS1
Neurodegenerative disorders, adult onset v1.74 AARS Louise Daugherty commented on gene: AARS: Review and rating submitted by Nick Beauchamp (Sheffield Diagnostic genetics Service), on behalf of Yorkshire and North East GLH for GMS Neurology specialist test group.
Neurodegenerative disorders, adult onset v1.72 AARS Nick Beauchamp reviewed gene: AARS: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Neurodegenerative disorders, adult onset v1.67 AARS Louise Daugherty Source Yorkshire and North East GLH was added to AARS.
Neurodegenerative disorders, adult onset v1.7 AARS Louise Daugherty reviewed gene: AARS: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Neurodegenerative disorders, adult onset v1.6 AARS Anthony Dallosso reviewed gene: AARS: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Current diagnostic: yes
Neurodegenerative disorders, adult onset v1.5 AARS Louise Daugherty Source NHS GMS was added to AARS.
Neurodegenerative disorders, adult onset v1.4 AARS Louise Daugherty Source South West GLH was added to AARS.
Neurodegenerative disorders, adult onset v0.2 AARS Rebecca Foulger gene: AARS was added
gene: AARS was added to Neurodegenerative disorders - adult onset. Sources: Expert Review Red
Mode of inheritance for gene: AARS was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown