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Fetal anomalies v0.3050 LRPPRC Zornitza Stark Marked gene: LRPPRC as ready
Fetal anomalies v0.3050 LRPPRC Zornitza Stark Gene: lrpprc has been classified as Amber List (Moderate Evidence).
Fetal anomalies v0.3050 LRPPRC Zornitza Stark Phenotypes for gene: LRPPRC were changed from LEIGH SYNDROME, FRENCH-CANADIAN TYPE to Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian) MIM#220111
Fetal anomalies v0.3049 LRPPRC Zornitza Stark Publications for gene: LRPPRC were set to
Fetal anomalies v0.3048 LRPPRC Zornitza Stark Classified gene: LRPPRC as Amber List (moderate evidence)
Fetal anomalies v0.3048 LRPPRC Zornitza Stark Gene: lrpprc has been classified as Amber List (Moderate Evidence).
Fetal anomalies v0.2946 LRPPRC Ain Roesley reviewed gene: LRPPRC: Rating: AMBER; Mode of pathogenicity: None; Publications: 32972427, 26510951, 21266382; Phenotypes: Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian) MIM#220111; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Fetal anomalies v0.0 LRPPRC Zornitza Stark gene: LRPPRC was added
gene: LRPPRC was added to Fetal anomalies. Sources: Expert Review Red,Genomics England PanelApp
Mode of inheritance for gene: LRPPRC was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: LRPPRC were set to LEIGH SYNDROME, FRENCH-CANADIAN TYPE