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the AGL gene, which encodes the glycogen debrancher enzyme, on chromosome 1p21." }, "synonyms": [ { "id": "DOID:2748", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2748", "name": "Glycogen storage disease, type III", "description": "" }, { "id": "DOID:2748", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2748", "name": "amylo 1,6 glucosidase deficiency", "description": "" }, { "id": "DOID:2748", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2748", "name": "deficiency of debranching enzyme", "description": "" }, { "id": "DOID:2748", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2748", "name": "deficiency of dextrin", "description": "" }, { "id": "DOID:2748", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:2748", "name": "Glycogen storage disease 3", "description": "" }, { "id": "MONDO:0009291", "resource": "MONDO", "url": 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"https://monarchinitiative.org/disease/MONDO:0009291", "name": "GDE deficiency", "description": "" }, { "id": "MONDO:0009291", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009291", "name": "GSD due to glycogen debranching enzyme deficiency", "description": "" }, { "id": "MONDO:0009291", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009291", "name": "GSD type 3", "description": "" }, { "id": "MONDO:0009291", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009291", "name": "GSDIII", "description": "" }, { "id": "MONDO:0009291", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009291", "name": "amylo 1,6 glucosidase deficiency", "description": "" }, { "id": "MONDO:0009291", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009291", "name": "amylo-1,6-glucosidase deficiency", "description": "" }, { "id": "MONDO:0009291", "resource": "MONDO", "url": 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