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Paediatric motor neuronopathies v1.57 HSPB1 Ivone Leong Phenotypes for gene: HSPB1 were changed from to Neuropathy, distal hereditary motor, type IIB, OMIM:608634; Charcot-Marie-Tooth disease, axonal, type 2F, OMIM:606595
Paediatric motor neuronopathies HSPB1 Arianna Tucci marked HSPB1 as ready
Paediatric motor neuronopathies HSPB1 Arianna Tucci reviewed HSPB1
Paediatric motor neuronopathies HSPB1 Alice Gardham classified HSPB1 as amber
Paediatric motor neuronopathies HSPB1 Alice Gardham marked HSPB1 as ready
Paediatric motor neuronopathies HSPB1 Alice Gardham classified HSPB1 as red
Paediatric motor neuronopathies HSPB1 Alice Gardham commented on HSPB1