{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009285", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "gamma-glutamyltranspeptidase deficiency"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009285", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009285", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009285", 
            "name": "GGT1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009285", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009285", 
            "name": "GGT deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009285", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009285", 
            "name": "glutathionuria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009285", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009285", 
            "name": "inborn glutathione hydrolase activity disorder"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009285", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009285", 
            "name": "GTG deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009285", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009285", 
            "name": "inborn error of glutathione hydrolase activity"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009285", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009285", 
            "name": "gamma-glutamyltransferase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111257", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111257", 
            "name": "GGT deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111257", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111257", 
            "name": "GGT1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111257", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111257", 
            "name": "GTG deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111257", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111257", 
            "name": "gamma-glutamyl transferase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111257", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111257", 
            "name": "glutathionuria"
        }, 
        {
            "url": "https://www.omim.org/entry/231950", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:231950", 
            "name": "Glutathionuria"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111257", 
        "description": "An amino acid metabolic disorder characterized by accumulation of glutathione in the plasma and urine that has_material_basis_in homozygous or compound heterozygous mutation in GGT1 on 22q11.23.", 
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        "id": "DOID:0111257", 
        "name": "gamma-glutamyl transpeptidase deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/231950", 
            "id": "231950", 
            "database": "MIM"
        }
    ]
}