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Retinal disorders v4.7 SPG7 Sarah Leigh Classified gene: SPG7 as Amber List (moderate evidence)
Retinal disorders v4.7 SPG7 Sarah Leigh Gene: spg7 has been classified as Amber List (Moderate Evidence).
Retinal disorders v4.6 SPG7 Sarah Leigh reviewed gene: SPG7: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Retinal disorders v4.6 SPG7 Sarah Leigh Mode of inheritance for gene: SPG7 was changed from to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Retinal disorders v4.5 SPG7 Sarah Leigh Phenotypes for gene: SPG7 were changed from to Spastic paraplegia 7, autosomal recessive, OMIM:607259; hereditary spastic paraplegia 7, MONDO:0011803
Retinal disorders v1.159 SPG7 Gavin Arno reviewed gene: SPG7: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Retinal disorders v1.137 SPG7 Ivone Leong Source NHS GMS was added to SPG7.