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Fetal anomalies v0.3192 FIG4 Zornitza Stark Marked gene: FIG4 as ready
Fetal anomalies v0.3192 FIG4 Zornitza Stark Gene: fig4 has been classified as Green List (High Evidence).
Fetal anomalies v0.3192 FIG4 Zornitza Stark Phenotypes for gene: FIG4 were changed from Charcot-Marie-Tooth disease, type 4J, OMIM:611228; Charcot-Marie-Tooth disease type 4J, MONDO:0012640; Yunis-Varon syndrome, OMIM:216340; Yunis-Varon syndrome, MONDO:0008995; ?Polymicrogyria, bilateral temporooccipital, OMIM:612691; Bilateral parasagittal parieto-occipital polymicrogyria, MONDO:0012986 to Yunis-Varon syndrome, OMIM:216340; Yunis-Varon syndrome, MONDO:0008995; ?Polymicrogyria, bilateral temporooccipital, OMIM:612691; Bilateral parasagittal parieto-occipital polymicrogyria, MONDO:0012986
Fetal anomalies v0.3191 FIG4 Zornitza Stark Publications for gene: FIG4 were set to
Fetal anomalies v0.3190 FIG4 Zornitza Stark Classified gene: FIG4 as Green List (high evidence)
Fetal anomalies v0.3190 FIG4 Zornitza Stark Gene: fig4 has been classified as Green List (High Evidence).
Fetal anomalies v0.0 FIG4 Zornitza Stark gene: FIG4 was added
gene: FIG4 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp
Mode of inheritance for gene: FIG4 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: FIG4 were set to Charcot-Marie-Tooth disease, type 4J, OMIM:611228; Charcot-Marie-Tooth disease type 4J, MONDO:0012640; Yunis-Varon syndrome, OMIM:216340; Yunis-Varon syndrome, MONDO:0008995; ?Polymicrogyria, bilateral temporooccipital, OMIM:612691; Bilateral parasagittal parieto-occipital polymicrogyria, MONDO:0012986