{
    "disease_id": "DOID:0111723",
    "recommended_name": {
        "id": "DOID:0111723",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111723",
        "name": "Jacobsen Syndrome",
        "description": "A chromosomal deletion syndrome that is characterized by growth retardation, psychomotor retardation, distinctive facial features, skeletal abnormalities, and isoimmune thrombocytopenia that has_material_basis_in deletion of terminal chromosome 11q."
    },
    "synonyms": [
        {
            "id": "DOID:0111723",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111723",
            "name": "Jacobsen distal 11q deletion syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111723",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111723",
            "name": "chromosome 11q deletion syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111723",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111723",
            "name": "partial 11q monosomy syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007838",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007838",
            "name": "Jacobsen syndrome",
            "description": "A multiple congenital anomaly/intellectual disability contiguous gene syndrome caused by partial deletion of the long arm of chromosome 11."
        },
        {
            "id": "MONDO:0007838",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007838",
            "name": "11q terminal deletion disorder",
            "description": ""
        },
        {
            "id": "MONDO:0007838",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007838",
            "name": "Del(11)(q23.3)",
            "description": ""
        },
        {
            "id": "MONDO:0007838",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007838",
            "name": "Del(11)(qter)",
            "description": ""
        },
        {
            "id": "MONDO:0007838",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007838",
            "name": "Jacobsen syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007838",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007838",
            "name": "Jacobsen syndrome, Isolated cases",
            "description": ""
        },
        {
            "id": "MONDO:0007838",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007838",
            "name": "distal deletion 11q",
            "description": ""
        },
        {
            "id": "MONDO:0007838",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007838",
            "name": "distal monosomy 11q",
            "description": ""
        },
        {
            "id": "MONDO:0007838",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007838",
            "name": "monosomy 11qter",
            "description": ""
        },
        {
            "id": "MONDO:0007838",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007838",
            "name": "telomeric deletion 11q",
            "description": ""
        },
        {
            "id": "MONDO:0007838",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007838",
            "name": "JBS",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
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    ],
    "unlinked_id_list": [],
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            "id": "DOID:0111723",
            "database": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111723",
            "categories": []
        },
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            "id": "MONDO:0007838",
            "database": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007838",
            "categories": []
        }
    ],
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                }
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                },
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    "glycans": [],
    "biomarkers": [],
    "association_flag": "1000",
    "record_id": "doid.0111723"
}