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Severe Paediatric Disorders v0.12 CPT1C Louise Daugherty reviewed gene: CPT1C: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 CPT1C Louise Daugherty Publications for gene CPT1C were updated from to 30847515
Severe Paediatric Disorders v0.10 CPT1C Louise Daugherty Added phenotypes ?Spastic paraplegia 73, autosomal dominant, 616282 for gene: CPT1C
Severe Paediatric Disorders v0.9 CPT1C Louise Daugherty Added phenotypes ?Spastic paraplegia 73, autosomal dominant, 616282 for gene: CPT1C
Severe Paediatric Disorders v0.9 CPT1C Louise Daugherty Added phenotypes ?Spastic paraplegia 73, autosomal dominant, 616282 for gene: CPT1C
Severe Paediatric Disorders v0.8 CPT1C Louise Daugherty Added phenotypes ?Spastic paraplegia 73, autosomal dominant, 616282 for gene: CPT1C
Severe Paediatric Disorders v0.8 CPT1C Louise Daugherty Mode of inheritance for gene CPT1C was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes ?Spastic paraplegia 73, autosomal dominant, 616282 for gene: CPT1C
Severe Paediatric Disorders v0.7 CPT1C Louise Daugherty Source Next Generation Children Project was added to CPT1C.
Severe Paediatric Disorders v0.5 CPT1C Louise Daugherty Source Expert Review Amber was added to CPT1C.
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Severe Paediatric Disorders v0.4 CPT1C Louise Daugherty gene: CPT1C was added
gene: CPT1C was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: CPT1C was set to