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Leukodystrophy - paediatric v0.151 SPG11 Zornitza Stark Publications for gene: SPG11 were set to
Leukodystrophy - paediatric v0.150 SPG11 Zornitza Stark changed review comment from: Complex SPG with central involvement, including white matter changes.
Sources: Expert list; to: Complex SPG with central involvement, including white matter changes. Variable age of onset, including in childhood.
Sources: Expert list
Leukodystrophy - paediatric v0.150 SPG11 Zornitza Stark edited their review of gene: SPG11: Changed publications: 18067136; Changed phenotypes: Spastic paraplegia 11, autosomal recessive, MIM# 604360
Leukodystrophy - paediatric v0.150 SPG11 Zornitza Stark Marked gene: SPG11 as ready
Leukodystrophy - paediatric v0.150 SPG11 Zornitza Stark Gene: spg11 has been classified as Green List (High Evidence).
Leukodystrophy - paediatric v0.150 SPG11 Zornitza Stark Classified gene: SPG11 as Green List (high evidence)
Leukodystrophy - paediatric v0.150 SPG11 Zornitza Stark Gene: spg11 has been classified as Green List (High Evidence).
Leukodystrophy - paediatric v0.149 SPG11 Zornitza Stark gene: SPG11 was added
gene: SPG11 was added to Leukodystrophy - paediatric. Sources: Expert list
Mode of inheritance for gene: SPG11 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: SPG11 were set to Spastic paraplegia 11, autosomal recessive, MIM# 604360
Review for gene: SPG11 was set to GREEN
Added comment: Complex SPG with central involvement, including white matter changes.
Sources: Expert list