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Fetal anomalies v0.1618 ALDH5A1 Zornitza Stark Marked gene: ALDH5A1 as ready
Fetal anomalies v0.1618 ALDH5A1 Zornitza Stark Gene: aldh5a1 has been classified as Red List (Low Evidence).
Fetal anomalies v0.1618 ALDH5A1 Zornitza Stark Phenotypes for gene: ALDH5A1 were changed from SUCCINATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY to Succinic semialdehyde dehydrogenase deficiency, MIM# 271980
Fetal anomalies v0.1617 ALDH5A1 Zornitza Stark Publications for gene: ALDH5A1 were set to
Fetal anomalies v0.1616 ALDH5A1 Zornitza Stark changed review comment from: Over 50 unrelated families reported. Intellectual disability is part of the phenotype, which also includes developmental delay, hypotonia, ataxia, seizures, hyperkinetic behaviour, aggression, and sleep disturbances.; to: Over 50 unrelated families reported. Typically presents post-natally with intellectual disability, hypotonia, ataxia, seizures, hyperkinetic behaviour, aggression, and sleep disturbances.
Fetal anomalies v0.1616 ALDH5A1 Zornitza Stark edited their review of gene: ALDH5A1: Changed rating: RED
Fetal anomalies v0.0 ALDH5A1 Zornitza Stark gene: ALDH5A1 was added
gene: ALDH5A1 was added to Fetal anomalies. Sources: Expert Review Red,Genomics England PanelApp
Mode of inheritance for gene: ALDH5A1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: ALDH5A1 were set to SUCCINATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY