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Muscular dystrophy and myopathy_Paediatric v0.188 MYMK Bryony Thompson Classified gene: MYMK as Green List (high evidence)
Muscular dystrophy and myopathy_Paediatric v0.188 MYMK Bryony Thompson Gene: mymk has been classified as Green List (High Evidence).
Muscular dystrophy and myopathy_Paediatric v0.187 MYMK Bryony Thompson Classified gene: MYMK as Green List (high evidence)
Muscular dystrophy and myopathy_Paediatric v0.187 MYMK Bryony Thompson Gene: mymk has been classified as Green List (High Evidence).
Muscular dystrophy and myopathy_Paediatric v0.186 MYMK Bryony Thompson Marked gene: MYMK as ready
Muscular dystrophy and myopathy_Paediatric v0.186 MYMK Bryony Thompson Gene: mymk has been classified as Red List (Low Evidence).
Muscular dystrophy and myopathy_Paediatric v0.186 MYMK Bryony Thompson gene: MYMK was added
gene: MYMK was added to Muscular dystrophy_Paediatric. Sources: Other
Mode of inheritance for gene: MYMK was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: MYMK were set to 32333597; 30065953
Phenotypes for gene: MYMK were set to Carey-Fineman-Ziter syndrome MONDO:0009700
Review for gene: MYMK was set to GREEN
gene: MYMK was marked as current diagnostic
Added comment: Carey-Fineman-Ziter syndrome is considered a congenital myopathy
Sources: Other