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- B2afe4a6e607b6130c745f4737d7724d0 hasDbXref "Orphanet:364" @default.
- B2afe4a6e607b6130c745f4737d7724d0 type Axiom @default.
- B2afe4a6e607b6130c745f4737d7724d0 annotatedProperty IAO_0000115 @default.
- B2afe4a6e607b6130c745f4737d7724d0 annotatedSource MONDO_0002413 @default.
- B2afe4a6e607b6130c745f4737d7724d0 annotatedTarget "Glycogenosis due to glucose-6-phosphatase (G6P) deficiency or glycogen storage disease, (GSD), type 1, is a group of inherited metabolic diseases, including types a and b, and characterized by poor tolerance to fasting, growth retardation and hepatomegaly resulting from accumulation of glycogen and fat in the liver." @default.