{
    "disease_id": "DOID:0070136", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013751", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013751", 
            "name": "cutis laxa, autosomal dominant 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013751", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013751", 
            "name": "FBLN5 autosomal dominant cutis laxa"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013751", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013751", 
            "name": "cutis laxa, autosomal dominant 2; ADCL2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013751", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013751", 
            "name": "autosomal dominant cutis laxa caused by mutation in FBLN5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013751", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013751", 
            "name": "ADCL2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013751", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013751", 
            "name": "cutis laxa, autosomal dominant type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070136", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070136", 
            "name": "ADCL2"
        }, 
        {
            "url": "https://www.omim.org/entry/614434", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:614434", 
            "name": "Cutis laxa, autosomal dominant, 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070136", 
        "description": "An autosomal dominant cutis laxa that has_material_basis_in heterozygous mutation in the FBLN5 gene on chromosome 14q32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070136", 
        "name": "autosomal dominant cutis laxa 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614434", 
            "id": "614434", 
            "database": "MIM"
        }
    ]
}