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Severe Paediatric Disorders v1.69 ADPRHL2 Sarah Leigh Phenotypes for gene: ADPRHL2 were changed from Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures OMIM:618170; neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures MONDO:0100095 to Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures OMIM:618170; neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures MONDO:0100095
Severe Paediatric Disorders v1.68 ADPRHL2 Sarah Leigh Phenotypes for gene: ADPRHL2 were changed from Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures, 618170 to Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures OMIM:618170; neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures MONDO:0100095
Severe Paediatric Disorders v1.67 ADPRHL2 Sarah Leigh Publications for gene: ADPRHL2 were set to 30847515
Severe Paediatric Disorders v0.17 ADPRHL2 Louise Daugherty Mode of inheritance for gene ADPRHL2 was changed from to BIALLELIC, autosomal or pseudoautosomal
Severe Paediatric Disorders v0.12 ADPRHL2 Louise Daugherty edited their review of gene: ADPRHL2: Added comment: Initial gene list (NGC_genelist-20190823_GREEN_dis_moi_forCuration_20200211.xlsx) collated by Dr Courtney French (University of Cambridge University Hospital NHS Foundation), Dr Karyn Megy (Clinical Feedback Lead, NIHR BioResource - Rare Diseases Study, University of Cambridge University Hospital NHS Foundation), Dr Alba Sanchis-Juan (NIHR BioResource - Rare Diseases Study, University of Cambridge University Hospital NHS Foundation) and Lucy Raymond (Professor of Medical Genetics and Neurodevelopment, University of Cambridge University Hospital NHS Foundation). Submitted to the PanelApp resource January 2020 on behalf of the Next Generation Children Project, Addenbrookes' Hospital, Cambridge. Gene Symbol submitted: ADPRS; Recommended initial gene rating: Green List (high evidence); Phenotypes: Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures, 618170 (3); Mode of inheritance: Autosomal recessive; Changed rating: AMBER
Severe Paediatric Disorders v0.11 ADPRHL2 Louise Daugherty Publications for gene ADPRHL2 were updated from to 30847515
Severe Paediatric Disorders v0.10 ADPRHL2 Louise Daugherty Added phenotypes Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures, 618170 for gene: ADPRHL2
Severe Paediatric Disorders v0.9 ADPRHL2 Louise Daugherty Added phenotypes Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures, 618170 for gene: ADPRHL2
Severe Paediatric Disorders v0.9 ADPRHL2 Louise Daugherty Added phenotypes Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures, 618170 for gene: ADPRHL2
Severe Paediatric Disorders v0.8 ADPRHL2 Louise Daugherty Added phenotypes Neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures, 618170 for gene: ADPRHL2
Severe Paediatric Disorders v0.6 ADPRHL2 Louise Daugherty Tag new-gene-name tag was added to gene: ADPRHL2.
Severe Paediatric Disorders v0.6 ADPRHL2 Louise Daugherty commented on gene: ADPRHL2
Severe Paediatric Disorders v0.7 ADPRHL2 Louise Daugherty Source Next Generation Children Project was added to ADPRHL2.
Severe Paediatric Disorders v0.5 ADPRHL2 Louise Daugherty Source Expert Review Green was added to ADPRHL2.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 ADPRHL2 Louise Daugherty gene: ADPRHL2 was added
gene: ADPRHL2 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: ADPRHL2 was set to