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Fetal anomalies v0.2067 LHX3 Zornitza Stark Marked gene: LHX3 as ready
Fetal anomalies v0.2067 LHX3 Zornitza Stark Gene: lhx3 has been classified as Red List (Low Evidence).
Fetal anomalies v0.2067 LHX3 Zornitza Stark Phenotypes for gene: LHX3 were changed from PITUITARY HORMONE DEFICIENCY COMBINED TYPE 3 to Pituitary hormone deficiency, combined, 3 (MIM#221750)
Fetal anomalies v0.2066 LHX3 Zornitza Stark Publications for gene: LHX3 were set to
Fetal anomalies v0.2065 LHX3 Zornitza Stark Classified gene: LHX3 as Red List (low evidence)
Fetal anomalies v0.2065 LHX3 Zornitza Stark Gene: lhx3 has been classified as Red List (Low Evidence).
Fetal anomalies v0.2064 LHX3 Zornitza Stark reviewed gene: LHX3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Pituitary hormone deficiency, combined, 3 (MIM#221750); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Fetal anomalies v0.0 LHX3 Zornitza Stark gene: LHX3 was added
gene: LHX3 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp
Mode of inheritance for gene: LHX3 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: LHX3 were set to PITUITARY HORMONE DEFICIENCY COMBINED TYPE 3