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Genetic Epilepsy v0.2641 PHGDH Zornitza Stark Marked gene: PHGDH as ready
Genetic Epilepsy v0.2641 PHGDH Zornitza Stark Gene: phgdh has been classified as Green List (High Evidence).
Genetic Epilepsy v0.2641 PHGDH Zornitza Stark Phenotypes for gene: PHGDH were changed from to Neu-Laxova syndrome 1, MIM# 256520; Phosphoglycerate dehydrogenase deficiency, MIM# 601815
Genetic Epilepsy v0.2640 PHGDH Zornitza Stark Publications for gene: PHGDH were set to
Genetic Epilepsy v0.2639 PHGDH Zornitza Stark Mode of inheritance for gene: PHGDH was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
Genetic Epilepsy v0.2638 PHGDH Zornitza Stark Mode of inheritance for gene: PHGDH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Genetic Epilepsy v0.2637 PHGDH Zornitza Stark changed review comment from: Well established gene-disease association, severity depends on amount of residual enzyme activity.; to: Well established gene-disease association, severity depends on amount of residual enzyme activity, seizures are part of the phenotype.
Genetic Epilepsy v0.0 PHGDH Zornitza Stark gene: PHGDH was added
gene: PHGDH was added to Genetic Epilepsy_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Epilepsy Flagship,Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: PHGDH was set to Unknown