{
    "disease_id": "DOID:0111459", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009258", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009258", 
            "name": "galactosemia, Duarte variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009258", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009258", 
            "name": "galactosemia, classic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009258", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009258", 
            "name": "galactose-1-phosphate uridylyltransferase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009258", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009258", 
            "name": "Galt deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009258", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009258", 
            "name": "galactosemia type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009258", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009258", 
            "name": "galactosemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009258", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009258", 
            "name": "galactose-1-phosphate uridyltransferase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009258", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009258", 
            "name": "classical galactosemia, homozygous duarte-type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111459", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111459", 
            "name": "GALT deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111459", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111459", 
            "name": "galactose-1-phosphate uridyltransferase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111459", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111459", 
            "name": "galactosemia type 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111459", 
        "description": "A galactosemia that has_material_basis_in homozygous or compund heterozygous mutation in GALT on chromosome 9p13.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111459", 
        "name": "classic galactosemia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111459#disease-associations", 
            "id": "0111459", 
            "database": "Alliance of Genome Resources"
        }
    ]
}