{
    "disease_id": "DOID:0111933", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010392", 
            "name": "glycogen storage disease due to phosphoglycerate kinase 1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010392", 
            "name": "glycogenosis due to phosphoglycerate kinase 1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010392", 
            "name": "PGK deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010392", 
            "name": "Pgk1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010392", 
            "name": "Phosphoglycerate kinase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010392", 
            "name": "glycogen storage disease caused by mutation in PGK1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010392", 
            "name": "GSD due to phosphoglycerate kinase 1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010392", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010392", 
            "name": "PGK1 glycogen storage disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111933", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111933", 
            "name": "PGK1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111933", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111933", 
            "name": "GSD due to phosphoglycerate kinase 1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111933", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111933", 
            "name": "glycogen storage disease due to phosphoglycerate kinase 1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111933", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111933", 
            "name": "glycogenosis due to phosphoglycerate kinase 1 deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111933", 
        "description": "A glucose metabolism disease characterized by impaired ability to break down glucose resulting in the variable presentation of hemolytic anemia, myopathy, and neurologic anomalies that has_material_basis_in hemizygous or homozygous mutation in PGK1 on chromosome Xq21.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111933", 
        "name": "phosphoglycerate kinase 1 deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111933#disease-associations", 
            "id": "0111933", 
            "database": "Alliance of Genome Resources"
        }
    ]
}