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Fetal anomalies v0.3041 LMOD1 Zornitza Stark Marked gene: LMOD1 as ready
Fetal anomalies v0.3041 LMOD1 Zornitza Stark Gene: lmod1 has been classified as Amber List (Moderate Evidence).
Fetal anomalies v0.3041 LMOD1 Zornitza Stark Phenotypes for gene: LMOD1 were changed from Megacystis Microcolon Intestinal Hypoperistalsis Syndrome (MMIH) to Megacystis-microcolon-intestinal hypoperistalsis syndrome 3, MIM# 619362
Fetal anomalies v0.3040 LMOD1 Zornitza Stark Publications for gene: LMOD1 were set to
Fetal anomalies v0.3039 LMOD1 Zornitza Stark Classified gene: LMOD1 as Amber List (moderate evidence)
Fetal anomalies v0.3039 LMOD1 Zornitza Stark Gene: lmod1 has been classified as Amber List (Moderate Evidence).
Fetal anomalies v0.2939 LMOD1 Ain Roesley reviewed gene: LMOD1: Rating: AMBER; Mode of pathogenicity: None; Publications: 28292896; Phenotypes: Megacystis-microcolon-intestinal hypoperistalsis syndrome 3, MIM# 619362; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Fetal anomalies v0.0 LMOD1 Zornitza Stark gene: LMOD1 was added
gene: LMOD1 was added to Fetal anomalies. Sources: Expert Review Red,Genomics England PanelApp
Mode of inheritance for gene: LMOD1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: LMOD1 were set to Megacystis Microcolon Intestinal Hypoperistalsis Syndrome (MMIH)