{
    "disease_id": "DOID:0060405",
    "recommended_name": {
        "id": "DOID:0060405",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060405",
        "name": "chromosome 17q23.1-q23.2 deletion syndrome",
        "description": "A chromosomal deletion syndrome that has_material_basis_in a chromosome 17q23.1-q23.2 deletion and that is characterized by characterized by developmental delay, microcephaly, short stature, heart defects and limb abnormalities."
    },
    "synonyms": [
        {
            "id": "DOID:0060405",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060405",
            "name": "17q23.1-q23.2 microdeletion syndrome",
            "description": ""
        },
        {
            "id": "DOID:0060405",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060405",
            "name": "17q23.1q23.2 microdeletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013238",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013238",
            "name": "chromosome 17q23.1-q23.2 deletion syndrome",
            "description": "17q23.1q23.2 microdeletion syndrome is a recently described syndrome characterized by developmental delay, microcephaly, short stature, heart defects and limb abnormalities."
        },
        {
            "id": "MONDO:0013238",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013238",
            "name": "17q23.1q23.2 microdeletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013238",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013238",
            "name": "Del(17)(q23.1q23.2)",
            "description": ""
        },
        {
            "id": "MONDO:0013238",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013238",
            "name": "monosomy 17q23.1-q23.2",
            "description": ""
        },
        {
            "id": "MONDO:0013238",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013238",
            "name": "monosomy 17q23.1q23.2",
            "description": ""
        },
        {
            "id": "MONDO:0013238",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013238",
            "name": "17q23.1-q23.2 microdeletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013238",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013238",
            "name": "chromosome 17q23.1-q23.2 deletion syndrome",
            "description": ""
        }
    ]
}