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Fetal anomalies v0.3672 GLUD1 Zornitza Stark Marked gene: GLUD1 as ready
Fetal anomalies v0.3672 GLUD1 Zornitza Stark Gene: glud1 has been classified as Red List (Low Evidence).
Fetal anomalies v0.3672 GLUD1 Zornitza Stark Phenotypes for gene: GLUD1 were changed from HYPERINSULINISM-HYPERAMMONEMIA SYNDROME to Hyperinsulinism-hyperammonemia syndrome, MIM#606762
Fetal anomalies v0.3671 GLUD1 Zornitza Stark Mode of inheritance for gene: GLUD1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Fetal anomalies v0.3670 GLUD1 Zornitza Stark changed review comment from: ID is not typically a feature.; to: Clinical presentation is typically postnatal.
Fetal anomalies v0.0 GLUD1 Zornitza Stark gene: GLUD1 was added
gene: GLUD1 was added to Fetal anomalies. Sources: Expert Review Red,Genomics England PanelApp
Mode of inheritance for gene: GLUD1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: GLUD1 were set to HYPERINSULINISM-HYPERAMMONEMIA SYNDROME