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Severe Paediatric Disorders v0.12 MYO18B Louise Daugherty reviewed gene: MYO18B: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 MYO18B Louise Daugherty Publications for gene MYO18B were updated from to 30847515
Severe Paediatric Disorders v0.11 MYO18B Louise Daugherty Mode of inheritance for gene MYO18B was changed from to BIALLELIC, autosomal or pseudoautosomal
Severe Paediatric Disorders v0.10 MYO18B Louise Daugherty Added phenotypes Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism, 616549 for gene: MYO18B
Severe Paediatric Disorders v0.9 MYO18B Louise Daugherty Added phenotypes Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism, 616549 for gene: MYO18B
Severe Paediatric Disorders v0.9 MYO18B Louise Daugherty Added phenotypes Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism, 616549 for gene: MYO18B
Severe Paediatric Disorders v0.8 MYO18B Louise Daugherty Added phenotypes Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism, 616549 for gene: MYO18B
Severe Paediatric Disorders v0.7 MYO18B Louise Daugherty Source Next Generation Children Project was added to MYO18B.
Severe Paediatric Disorders v0.5 MYO18B Louise Daugherty Source Expert Review Green was added to MYO18B.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 MYO18B Louise Daugherty gene: MYO18B was added
gene: MYO18B was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: MYO18B was set to