{
    "disease_id": "DOID:10587",
    "recommended_name": {
        "id": "DOID:10587",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:10587",
        "name": "Krabbe disease",
        "description": ""
    },
    "synonyms": [
        {
            "id": "DOID:10587",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:10587",
            "name": "Diffuse globoid body sclerosis",
            "description": ""
        },
        {
            "id": "DOID:10587",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:10587",
            "name": "GLOBOID CELL LEUKOENCEPHALOPATHY",
            "description": ""
        },
        {
            "id": "DOID:10587",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:10587",
            "name": "Galactosylceramide beta-galactosidase deficiency",
            "description": ""
        },
        {
            "id": "DOID:10587",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:10587",
            "name": "Krabbe's disease",
            "description": ""
        },
        {
            "id": "DOID:10587",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:10587",
            "name": "Krabbe's leukodystrophy",
            "description": ""
        },
        {
            "id": "DOID:10587",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:10587",
            "name": "beta galactocerebrosidase deficiency",
            "description": ""
        },
        {
            "id": "DOID:10587",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:10587",
            "name": "globoid cell leukodystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0009499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009499",
            "name": "Krabbe disease",
            "description": "Krabbe disease is a lysosomal disorder that affects the white matter of the central and peripheral nervous systems. It includes infantile, late-infantile/juvenile and adult forms."
        },
        {
            "id": "MONDO:0009499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009499",
            "name": "Krabbe's disease",
            "description": ""
        },
        {
            "id": "MONDO:0009499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009499",
            "name": "Krabbe disease",
            "description": ""
        },
        {
            "id": "MONDO:0009499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009499",
            "name": "beta galactocerebrosidase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009499",
            "name": "galactosylceramide Beta-galactosidase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009499",
            "name": "globoid cell leukodystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0009499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009499",
            "name": "Krabbe leukodystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0009499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009499",
            "name": "galactocerebrosidase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009499",
            "name": "GALC deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009499",
            "name": "globoid cell leukoencephalopathy",
            "description": ""
        },
        {
            "id": "MONDO:0009499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009499",
            "name": "galactosylceramidase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009499",
            "name": "Krabbe's leukodystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0009499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009499",
            "name": "GLD",
            "description": ""
        },
        {
            "id": "MONDO:0009499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009499",
            "name": "diffuse globoid body sclerosis",
            "description": ""
        },
        {
            "id": "MONDO:0009499",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009499",
            "name": "galactosylceramide lipidosis",
            "description": ""
        },
        {
            "id": "MIM:245200",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/245200",
            "name": "Leukodystrophy, globoid cell",
            "description": "Leukodystrophy, globoid cell"
        }
    ]
}