{
    "disease_id": "DOID:0070135", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009052", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009052", 
            "name": "cutis laxa, autosomal recessive, type 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009052", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009052", 
            "name": "ARCL1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009052", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009052", 
            "name": "ARCL1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009052", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009052", 
            "name": "cutis laxa, autosomal recessive, type IA; ARCL1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009052", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009052", 
            "name": "cutis laxa, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009052", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009052", 
            "name": "cutis laxa, autosomal recessive, type IA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070135", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070135", 
            "name": "ARCL1A"
        }, 
        {
            "url": "https://www.omim.org/entry/219100", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:219100", 
            "name": "Cutis laxa, autosomal recessive, 1A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070135", 
        "description": "An autosomal recessive cutis laxa type I that has_material_basis_in homozygous or compound heterozygous mutation in the FBLN5 gene on chromosome 14q32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070135", 
        "name": "autosomal recessive cutis laxa type IA"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/219100", 
            "id": "219100", 
            "database": "MIM"
        }
    ]
}