{
    "disease_id": "DOID:0070130", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007411", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007411", 
            "name": "cutis laxa, autosomal dominant 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007411", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007411", 
            "name": "ELN autosomal dominant cutis laxa"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007411", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007411", 
            "name": "ADCL1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007411", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007411", 
            "name": "autosomal dominant cutis laxa caused by mutation in ELN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007411", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007411", 
            "name": "cutis laxa, autosomal dominant type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007411", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007411", 
            "name": "cutis laxa, autosomal dominant 1; ADCL1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070130", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070130", 
            "name": "ADCL1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070130", 
        "description": "An autosomal dominant cutis laxa that has_material_basis_in heterozygous mutations in the ELN gene on chromosome 7q11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070130", 
        "name": "autosomal dominant cutis laxa 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070130#disease-associations", 
            "id": "0070130", 
            "database": "Alliance of Genome Resources"
        }
    ]
}