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| Genetic Epilepsy v2.2 | FGFR1 | Zornitza Stark Mode of inheritance for gene: FGFR1 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v2.1 | FGFR1 | Zornitza Stark reviewed gene: FGFR1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v2.0 | FGFR1 | Gene migrated from ENSG00000077782 to ENSG00000077782 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.2663 | FGFR1 | Ain Roesley Marked gene: FGFR1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.2663 | FGFR1 | Ain Roesley Gene: fgfr1 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.2663 | FGFR1 | Ain Roesley Classified gene: FGFR1 as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.2663 | FGFR1 | Ain Roesley Gene: fgfr1 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genetic Epilepsy v0.2662 | FGFR1 |
Ain Roesley gene: FGFR1 was added gene: FGFR1 was added to Genetic Epilepsy. Sources: Literature Mode of inheritance for gene: FGFR1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Publications for gene: FGFR1 were set to 26937548; 31512363; 23812909; 26931467 Phenotypes for gene: FGFR1 were set to Hartsfield syndrome (MIM#615465) Review for gene: FGFR1 was set to GREEN gene: FGFR1 was marked as current diagnostic Added comment: Seizures is part of the phenotypic spectrum of Hartsfield Syndrome *rare reports of AR Hartsfield Sources: Literature |
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