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Fetal anomalies v0.3396 MYH7 Zornitza Stark Marked gene: MYH7 as ready
Fetal anomalies v0.3396 MYH7 Zornitza Stark Gene: myh7 has been classified as Green List (High Evidence).
Fetal anomalies v0.3396 MYH7 Zornitza Stark Phenotypes for gene: MYH7 were changed from Cardiomyopathy, hypertrophic, 1, OMIM:192600; Laing early-onset distal myopathy, MONDO:0008050; Left ventricular noncompaction 5, OMIM:613426; Cardiomyopathy, dilated, 1S, OMIM:613426; Hypertrophic cardiomyopathy 1, MONDO:0008647; Laing distal myopathy, OMIM:160500; Dilated cardiomyopathy 1S, MONDO:0013262 to Ebstein anomaly; Laing distal myopathy, MIM# 160500
Fetal anomalies v0.3395 MYH7 Zornitza Stark Publications for gene: MYH7 were set to 22859017; 26337809; 25547560
Fetal anomalies v0.3394 MYH7 Zornitza Stark Mode of pathogenicity for gene: MYH7 was changed from to Other
Fetal anomalies v0.3393 MYH7 Zornitza Stark Classified gene: MYH7 as Green List (high evidence)
Fetal anomalies v0.3393 MYH7 Zornitza Stark Gene: myh7 has been classified as Green List (High Evidence).
Fetal anomalies v0.0 MYH7 Zornitza Stark gene: MYH7 was added
gene: MYH7 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp
Mode of inheritance for gene: MYH7 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: MYH7 were set to 22859017; 26337809; 25547560
Phenotypes for gene: MYH7 were set to Cardiomyopathy, hypertrophic, 1, OMIM:192600; Laing early-onset distal myopathy, MONDO:0008050; Left ventricular noncompaction 5, OMIM:613426; Cardiomyopathy, dilated, 1S, OMIM:613426; Hypertrophic cardiomyopathy 1, MONDO:0008647; Laing distal myopathy, OMIM:160500; Dilated cardiomyopathy 1S, MONDO:0013262