{
    "disease_id": "DOID:0060363", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010613", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010613", 
            "name": "inborn glycerol kinase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010613", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010613", 
            "name": "rare inborn error of glycerol kinase activity"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010613", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010613", 
            "name": "glycerol kinase deficiency; GKD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010613", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010613", 
            "name": "GK1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010613", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010613", 
            "name": "GKD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010613", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010613", 
            "name": "inborn error of glycerol kinase activity"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010613", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010613", 
            "name": "inborn glycerol kinase activity disorder"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010613", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010613", 
            "name": "hyperglycerolemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010613", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010613", 
            "name": "GK deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060363", 
        "description": "An inherited metabolic disorder characterized_by wide range of phenotypic variability; patients can have severe metabolic and CNS abnormalities, while others possess hyperglycerolemia and glyceroluria with no other apparent phenotype and that has_material_basis_in mutation in the GK gene on chromosome Xp21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060363", 
        "name": "glycerol kinase deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060363#disease-associations", 
            "id": "0060363", 
            "database": "Alliance of Genome Resources"
        }
    ]
}