{
    "disease_id": "DOID:0070140", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0027462", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0027462", 
            "name": "autosomal recessive cutis laxa type 2c"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0027462", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0027462", 
            "name": "ARCL2C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0027462", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0027462", 
            "name": "cutis laxa, autosomal recessive, type IIC; ARCL2C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0027462", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0027462", 
            "name": "cutis laxa, autosomal recessive, type 2C"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070140", 
        "description": "An autosomal recessive cutis laxa type II classic type characterized by cardiovascular involvement that has_material_basis_in homozygous mutation in the ATP6V1E1 gene on chromosome 22q11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070140", 
        "name": "autosomal recessive cutis laxa type IIC"
    }, 
    "evidence": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0027462", 
            "id": "0027462", 
            "database": "MONDO"
        }, 
        {
            "url": "https://www.omim.org/entry/617402", 
            "id": "617402", 
            "database": "MIM"
        }
    ]
}