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Hereditary spastic paraplegia, childhood onset v2.98 KIDINS220 Arina Puzriakova Phenotypes for gene: KIDINS220 were changed from Spastic paraplegia, intellectual disability, nystagmus, and obesity, 617296 to Spastic paraplegia, intellectual disability, nystagmus, and obesity, OMIM:617296
Hereditary spastic paraplegia, childhood onset v2.58 KIDINS220 Arina Puzriakova Publications for gene: KIDINS220 were set to 27005418; 29667355
Hereditary spastic paraplegia, childhood onset v1.133 KIDINS220 Louise Daugherty Deleted their comment
Hereditary spastic paraplegia, childhood onset v1.133 KIDINS220 Louise Daugherty Phenotypes for gene: KIDINS220 were changed from Spastic paraplegia, intellectual disability, nystagmus, and obesity 617296 to Spastic paraplegia, intellectual disability, nystagmus, and obesity, 617296
Hereditary spastic paraplegia, childhood onset v1.132 KIDINS220 Louise Daugherty Publications for gene: KIDINS220 were set to
Hereditary spastic paraplegia, childhood onset v1.75 KIDINS220 Louise Daugherty Source Yorkshire and North East GLH was added to KIDINS220.
Hereditary spastic paraplegia, childhood onset v1.74 KIDINS220 Nick Beauchamp reviewed gene: KIDINS220: Rating: GREEN; Mode of pathogenicity: None; Publications: 27005418, 29667355; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Hereditary spastic paraplegia, childhood onset v1.74 KIDINS220 Louise Daugherty commented on gene: KIDINS220: Rating and review submitted on behalf of James Polke (Neurogenetics Laboratory,Institute of Neurology, London), on behalf of London North GLH for GMS Neurology specialist test group.
Hereditary spastic paraplegia, childhood onset v1.48 KIDINS220 Louise Daugherty reviewed gene: KIDINS220: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Hereditary spastic paraplegia, childhood onset v1.6 KIDINS220 James Polke reviewed gene: KIDINS220: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Spastic paraplegia, intellectual disability, nystagmus, and obesity, autosomal dominant, 617296; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Hereditary spastic paraplegia, childhood onset v1.5 KIDINS220 Louise Daugherty Source NHS GMS was added to KIDINS220.
Hereditary spastic paraplegia, childhood onset v1.4 KIDINS220 Louise Daugherty Source London North GLH was added to KIDINS220.
Hereditary spastic paraplegia, childhood onset v1.3 KIDINS220 Louise Daugherty Added phenotypes Spastic paraplegia, intellectual disability, nystagmus, and obesity 617296 for gene: KIDINS220
Hereditary spastic paraplegia, childhood onset v0.62 KIDINS220 Arianna Tucci commented on gene: KIDINS220
Hereditary spastic paraplegia, childhood onset v0.6 KIDINS220 Sarah Leigh gene: KIDINS220 was added
gene: KIDINS220 was added to Hereditary spastic paraplegia - childhood onset. Sources: Other,Expert Review Green
Mode of inheritance for gene: KIDINS220 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: KIDINS220 were set to Spastic paraplegia, intellectual disability, nystagmus, and obesity 617296