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Congenital myopathy v3.56 LGI4 Arina Puzriakova Phenotypes for gene: LGI4 were changed from Arthrogryposis Multiplex Congenita; Arthrogryposis multiplex congenita, neurogenic, with myelin defect, 617468; AMCNMY to Arthrogryposis multiplex congenita 1, neurogenic, with myelin defect, OMIM:617468
Congenital myopathy v1.221 LGI4 Louise Daugherty Source NHS GMS was added to LGI4.
Phenotypes for gene: LGI4 were changed from Arthrogryposis Multiplex Congenita; Arthrogryposis multiplex congenita, neurogenic, with myelin defect, 617468; AMCNMY to Arthrogryposis Multiplex Congenita; Arthrogryposis multiplex congenita, neurogenic, with myelin defect, 617468; AMCNMY
Congenital myopathy v1.199 LGI4 Louise Daugherty Classified gene: LGI4 as Red List (low evidence)
Congenital myopathy v1.199 LGI4 Louise Daugherty Added comment: Comment on list classification: Changed from Green to Red. Updated rating from Anna Sarkozy as a result of GLH Test Group prior to sign off, gene not for CMY
Congenital myopathy v1.199 LGI4 Louise Daugherty Gene: lgi4 has been classified as Red List (Low Evidence).
Congenital myopathy LGI4 Louise Daugherty classified LGI4 as green
Congenital myopathy LGI4 Louise Daugherty added LGI4 to panel
Congenital myopathy LGI4 Louise Daugherty reviewed LGI4