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Hereditary ataxia with onset in adulthood v1.171 FRMD4A Louise Daugherty edited their review of gene: FRMD4A: Added comment: This panel was initially created as a merge of genomic entities from the following Rare Disease 100K panels -Hereditary ataxia v1.148 - Brain channelopathy v1.46. This gene was RED and external expert review from Wessex and West Midlands GLH for GMS Neurology specialist test group for R54 agrees this gene should remain RED; Changed rating: RED
Hereditary ataxia with onset in adulthood v1.160 FRMD4A Louise Daugherty Mode of inheritance for gene: FRMD4A was changed from to BIALLELIC, autosomal or pseudoautosomal
Hereditary ataxia with onset in adulthood v1.9 FRMD4A Louise Daugherty Added phenotypes Agenesis of corpus callosum with facial anomalies and cerebellar ataxia for gene: FRMD4A
Hereditary ataxia with onset in adulthood v1.8 FRMD4A Louise Daugherty reviewed gene: FRMD4A: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Hereditary ataxia with onset in adulthood v1.7 FRMD4A Tracy Lester reviewed gene: FRMD4A: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Agenesis of corpus callosum with facial anomalies and cerebellar ataxia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Hereditary ataxia with onset in adulthood v1.2 FRMD4A Louise Daugherty Source NHS GMS was added to FRMD4A.
Hereditary ataxia with onset in adulthood v1.1 FRMD4A Louise Daugherty gene: FRMD4A was added
gene: FRMD4A was added to Hereditary ataxia - adult onset. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: FRMD4A was set to