{
    "disease_id": "DOID:0070233", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013897", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013897", 
            "name": "aneurysm, aortic and cerebral, with arterial tortuosity and skeletal manifestations"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013897", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013897", 
            "name": "Loeys-Dietz syndrome 4; LDS4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013897", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013897", 
            "name": "Loeys-Dietz syndrome type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013897", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013897", 
            "name": "Loeys-Dietz syndrome caused by mutation in TGFB2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013897", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013897", 
            "name": "TGFB2 Loeys-Dietz syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013897", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013897", 
            "name": "LDS4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070233", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070233", 
            "name": "LDS4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070233", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070233", 
            "name": "Aneurysm, aortic and cerebral, with arterial tortuosity and skeletal manifestations"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070233", 
        "description": "A Loeys-Dietz syndrome that has_material_basis_in heterozygous mutation in the TGFB2 gene on chromosome 1q41.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070233", 
        "name": "Loeys-Dietz syndrome 4"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614816", 
            "id": "614816", 
            "database": "MIM"
        }
    ]
}