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Fetal anomalies v0.1963 IDH1 Zornitza Stark Marked gene: IDH1 as ready
Fetal anomalies v0.1963 IDH1 Zornitza Stark Gene: idh1 has been classified as Red List (Low Evidence).
Fetal anomalies v0.1963 IDH1 Zornitza Stark Phenotypes for gene: IDH1 were changed from Maffucci syndrome 614569; Ollier disease/ Dyschondroplasia 166000; Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria 614875 to Ollier disease MONDO:0008145; Maffucci syndrome MONDO:0013808
Fetal anomalies v0.1962 IDH1 Zornitza Stark Publications for gene: IDH1 were set to 22057234; 22057236; 22025298; 24049096
Fetal anomalies v0.1961 IDH1 Zornitza Stark Mode of inheritance for gene: IDH1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to Other
Fetal anomalies v0.1960 IDH1 Zornitza Stark Classified gene: IDH1 as Red List (low evidence)
Fetal anomalies v0.1960 IDH1 Zornitza Stark Gene: idh1 has been classified as Red List (Low Evidence).
Fetal anomalies v0.1933 IDH1 Ain Roesley reviewed gene: IDH1: Rating: RED; Mode of pathogenicity: None; Publications: 34393643, 34588213, 34624834, 34720940; Phenotypes: Ollier disease MONDO:0008145, Maffucci syndromeMONDO:0013808; Mode of inheritance: Other; Current diagnostic: yes
Fetal anomalies v0.0 IDH1 Zornitza Stark gene: IDH1 was added
gene: IDH1 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp
Mode of inheritance for gene: IDH1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: IDH1 were set to 22057234; 22057236; 22025298; 24049096
Phenotypes for gene: IDH1 were set to Maffucci syndrome 614569; Ollier disease/ Dyschondroplasia 166000; Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria 614875