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| Glycogen storage disease v0.3 | AGL | Emma Ashton reviewed gene: AGL: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Glycogen storage disease v0.3 | AGL | Carol Hardy reviewed gene: AGL: Rating: GREEN; Mode of pathogenicity: ; Publications: 20301788; Phenotypes: Glycogen storage disease IIIa, 232400, Glycogen storage disease IIIb, 232400; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Glycogen storage disease v0.2 | AGL |
Ivone Leong gene: AGL was added gene: AGL was added to Glycogen storage disease. Sources: Expert Review Green,London North GLH,Wessex and West Midlands GLH,NHS GMS Mode of inheritance for gene: AGL was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: AGL were set to 20301788 Phenotypes for gene: AGL were set to Glycogen storage disease IIIb, 232400; Glycogen storage disease IIIa, 232400 |
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