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Mitochondrial neurogastrointestinal encephalopathy v1.2 TYMP Achchuthan Shanmugasundram Added comment: Comment on phenotypes: This gene has been associated with relevant phenotypes in OMIM (MIM #603041) and the OMIM record was last accessed on 20 December 2025.
Mitochondrial neurogastrointestinal encephalopathy v1.2 TYMP Achchuthan Shanmugasundram Phenotypes for gene: TYMP were changed from to Mitochondrial DNA depletion syndrome 1 (MNGIE type), OMIM:603041; mitochondrial DNA depletion syndrome 1, MONDO:0011283
Mitochondrial neurogastrointestinal encephalopathy v1.1 Sarah Leigh Panel version 1.0 has been signed off on 2023-09-14
Mitochondrial neurogastrointestinal encephalopathy v1.0 Sarah Leigh promoted panel to version 1.0
Mitochondrial neurogastrointestinal encephalopathy v0.3 Sarah Leigh Panel types changed to GMS Rare Disease; GMS signed-off
Mitochondrial neurogastrointestinal encephalopathy v0.2 Achchuthan Shanmugasundram Panel status changed from internal to public
Mitochondrial neurogastrointestinal encephalopathy v0.1 TYMP Achchuthan Shanmugasundram reviewed gene: TYMP: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial neurogastrointestinal encephalopathy v0.1 TYMP Achchuthan Shanmugasundram gene: TYMP was added
gene: TYMP was added to Mitochondrial neurogastrointestinal encephalopathy. Sources: NHS GMS,Expert Review Green
Mode of inheritance for gene: TYMP was set to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial neurogastrointestinal encephalopathy v0.0 Achchuthan Shanmugasundram Added Panel Mitochondrial neurogastrointestinal encephalopathy
Set list of related panels to R394
Set panel types to: GMS Rare Disease