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Likely inborn error of metabolism v8.71 FECH Achchuthan Shanmugasundram Publications for gene: FECH were set to 27604308
Likely inborn error of metabolism v8.70 FECH Achchuthan Shanmugasundram Added comment: Comment on phenotypes: OMIM accessed on 22 October 2025
Likely inborn error of metabolism v8.70 FECH Achchuthan Shanmugasundram Phenotypes for gene: FECH were changed from Protoporphyria, erythropoietic, 1 177000 to Protoporphyria, erythropoietic, 1, OMIM:177000; protoporphyria, erythropoietic, 1, MONDO:0008319
Likely inborn error of metabolism v8.55 FECH Sharon Whatley reviewed gene: FECH: Rating: GREEN; Mode of pathogenicity: None; Publications: 7857832, 16911284, 39969427, 32873934, 38940544, 11753383, 16385445; Phenotypes: 177000; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Likely inborn error of metabolism v1.120 FECH Sarah Leigh Classified gene: FECH as Green List (high evidence)
Likely inborn error of metabolism v1.120 FECH Sarah Leigh Added comment: Comment on list classification: This gene was part of an initial gene list collated by Emma Ashton on behalf of the London North GLH, for GMS Metabolic Consensus Specialist Test Group. Additional information was not provided, such as mode of inheritance and phenotype.
Associated with phenotype in OMIM and not in Gen2Phen. At least 16 variants identified in unrelated cases.
Likely inborn error of metabolism v1.120 FECH Sarah Leigh Gene: fech has been classified as Green List (High Evidence).
Likely inborn error of metabolism v1.119 FECH Sarah Leigh Phenotypes for gene: FECH were changed from Protoporphyria, erythropoietic, 1 177000 to Protoporphyria, erythropoietic, 1 177000
Likely inborn error of metabolism v1.119 FECH Sarah Leigh Phenotypes for gene: FECH were changed from Erythropoietic protoporphyria, mild variant; Erythropoietic protoporphyria (Porphyrias with acute painful photosensitivity) to Protoporphyria, erythropoietic, 1 177000
Likely inborn error of metabolism v1.47 FECH Ivone Leong Source NHS GMS was added to FECH.
Source London North GLH was added to FECH.
Likely inborn error of metabolism v0.4 FECH Ellen McDonagh gene: FECH was added
gene: FECH was added to Inborn errors of metabolism. Sources: Expert Review Amber
Mode of inheritance for gene: FECH was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: FECH were set to 27604308
Phenotypes for gene: FECH were set to Erythropoietic protoporphyria, mild variant; Erythropoietic protoporphyria (Porphyrias with acute painful photosensitivity)