| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Mitochondrial disorders v1.438 | FGF12 | Sarah Leigh Phenotypes for gene: FGF12 were changed from Epileptic encephalopathy, early infantile, 47 617166 to Epileptic encephalopathy, early infantile, 47 617166 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mitochondrial disorders v1.437 | FGF12 | Sarah Leigh Phenotypes for gene: FGF12 were changed from to Epileptic encephalopathy, early infantile, 47 617166 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mitochondrial disorders v1.437 | FGF12 | Sarah Leigh Publications for gene: FGF12 were set to | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mitochondrial disorders v1.423 | FGF12 | Sarah Leigh reviewed gene: FGF12: Rating: RED; Mode of pathogenicity: ; Publications: 29903433, 27164707, 27872899; Phenotypes: Epileptic encephalopathy, early infantile, 47 617166; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mitochondrial disorders v1.422 | FGF12 |
Sarah Leigh gene: FGF12 was added gene: FGF12 was added to Mitochondrial disorders. Sources: Expert list Mode of inheritance for gene: FGF12 was set to |
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||