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Interstitial Lung Disease v0.246 FGFR2 Zornitza Stark Marked gene: FGFR2 as ready
Interstitial Lung Disease v0.246 FGFR2 Zornitza Stark Gene: fgfr2 has been classified as Amber List (Moderate Evidence).
Interstitial Lung Disease v0.246 FGFR2 Zornitza Stark Phenotypes for gene: FGFR2 were changed from to Ectrodactyly, pulmonary acinar dysplasia
Interstitial Lung Disease v0.245 FGFR2 Zornitza Stark Publications for gene: FGFR2 were set to
Interstitial Lung Disease v0.244 FGFR2 Zornitza Stark Mode of inheritance for gene: FGFR2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Interstitial Lung Disease v0.243 FGFR2 Zornitza Stark Classified gene: FGFR2 as Amber List (moderate evidence)
Interstitial Lung Disease v0.243 FGFR2 Zornitza Stark Gene: fgfr2 has been classified as Amber List (Moderate Evidence).
Interstitial Lung Disease v0.183 FGFR2 Suzanna Lindsey-Temple reviewed gene: FGFR2: Rating: AMBER; Mode of pathogenicity: None; Publications: PMID: 27323706; Phenotypes: Crouzon, Apert, Antley-Bixler, Pfeiffer - respiratory distress of the newborn associated with upper airway obstruction/ tracheal anomalies.; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Interstitial Lung Disease v0.0 FGFR2 Zornitza Stark gene: FGFR2 was added
gene: FGFR2 was added to Interstitial Lung Disease_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: FGFR2 was set to Unknown