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Severe Paediatric Disorders v0.17 CCT5 Louise Daugherty Mode of inheritance for gene CCT5 was changed from to BIALLELIC, autosomal or pseudoautosomal
Severe Paediatric Disorders v0.12 CCT5 Louise Daugherty reviewed gene: CCT5: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 CCT5 Louise Daugherty Publications for gene CCT5 were updated from to 30847515
Severe Paediatric Disorders v0.10 CCT5 Louise Daugherty Added phenotypes Neuropathy, hereditary sensory, with spastic paraplegia, 256840 for gene: CCT5
Severe Paediatric Disorders v0.9 CCT5 Louise Daugherty Added phenotypes Neuropathy, hereditary sensory, with spastic paraplegia, 256840 for gene: CCT5
Severe Paediatric Disorders v0.9 CCT5 Louise Daugherty Added phenotypes Neuropathy, hereditary sensory, with spastic paraplegia, 256840 for gene: CCT5
Severe Paediatric Disorders v0.8 CCT5 Louise Daugherty Added phenotypes Neuropathy, hereditary sensory, with spastic paraplegia, 256840 for gene: CCT5
Severe Paediatric Disorders v0.7 CCT5 Louise Daugherty Source Next Generation Children Project was added to CCT5.
Severe Paediatric Disorders v0.5 CCT5 Louise Daugherty Source Expert Review Green was added to CCT5.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 CCT5 Louise Daugherty gene: CCT5 was added
gene: CCT5 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: CCT5 was set to