Genomics England

ZFYVE26

zinc finger FYVE-type containing 26

OMIM: 612012

Panel	Mode of inheritance	Details
Filter panels9 panels
Green in DDG2P Component of the following Super Panels: - Paediatric disorders Signed-off version 8.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes SPASTIC PARAPLEGIA AUTOSOMAL RECESSIVE TYPE 15 270700
Green in Hereditary ataxia, adult onset Component of the following Super Panels: - Adult-onset neurological disorders Signed-off version 9.4	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Spastic paraplegia 15, autosomal recessive, OMIM:270700
Green in Hereditary neuropathy or pain disorder R-numbers: R78 Signed-off version 8.30	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Spastic paraplegia 15, autosomal recessive, OMIM:270700
Green in Hereditary spastic paraplegia, adult onset Component of the following Super Panels: - Adult-onset neurological disorders Signed-off version 6.13	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Spastic paraplegia 15, autosomal recessive, OMIM:270700
Green in Hereditary spastic paraplegia, childhood onset R-numbers: R61 Signed-off version 9.7	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Spastic paraplegia 15, autosomal recessive, OMIM:270700
Green in Intellectual disability Component of the following Super Panels: - Hypotonic infant - Leukodystrophy, childhood onset - Paediatric disorders Signed-off version 11.0	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Spastic paraplegia 15, autosomal recessive, OMIM:270700
Green in Leukodystrophy, adult onset R-numbers: R62 Signed-off version 7.8	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Spastic paraplegia 15, autosomal recessive, 270700
Green in Retinal disorders R-numbers: R32 Signed-off version 9.14	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Spastic paraplegia 15, autosomal recessive OMIM:270700
Green in White matter disorders and cerebral calcification - childhood onset Component of the following Super Panels: - Leukodystrophy, childhood onset - Paediatric disorders Signed-off version 8.6	BIALLELIC, autosomal or pseudoautosomal	Phenotypes Spastic paraplegia 15, autosomal recessive, OMIM:270700