{
    "disease_id": "DOID:0060427",
    "recommended_name": {
        "id": "DOID:0060427",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060427",
        "name": "chromosome Xp21 deletion syndrome",
        "description": "A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome Xp21 region."
    },
    "synonyms": [
        {
            "id": "DOID:0060427",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060427",
            "name": "Xp21 microdeletion syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060427",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060427",
            "name": "complex glycerol kinase deficiency",
            "description": ""
        },
        {
            "id": "DOID:0060427",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060427",
            "name": "monosomy Xp21",
            "description": ""
        },
        {
            "id": "MONDO:0010399",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010399",
            "name": "chromosome Xp21 deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010399",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010399",
            "name": "chromosome Xp21 deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010399",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010399",
            "name": "complex glycerol kinase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010399",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010399",
            "name": "Xp21 microdeletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010399",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010399",
            "name": "monosomy Xp21",
            "description": ""
        },
        {
            "id": "MONDO:0010399",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010399",
            "name": "Xp21 contiguous gene deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010399",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010399",
            "name": "Complex Glycerol kinase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010399",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010399",
            "name": "Del(X)(p21)",
            "description": ""
        },
        {
            "id": "MONDO:0010399",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010399",
            "name": "Glycerol kinase deficiency-contiguous gene syndrome",
            "description": ""
        }
    ]
}