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| Glycogen storage disease v0.3 | FBP1 | Carol Hardy reviewed gene: FBP1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Fructose-1,6-bisphosphatase deficiency 229700; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Glycogen storage disease v0.2 | FBP1 |
Ivone Leong gene: FBP1 was added gene: FBP1 was added to Glycogen storage disease. Sources: Expert Review Green,Wessex and West Midlands GLH,NHS GMS Mode of inheritance for gene: FBP1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: FBP1 were set to Fructose-1,6-bisphosphatase deficiency 229700 |
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