{
    "disease_id": "DOID:0070143", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0070143", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070143", 
            "name": "De Barsy syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070143", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070143", 
            "name": "cutis laxa-corneal clouding-intellectual disability syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070143", 
        "description": "A cutis laxa characterized by a progeria-like appearance, ophthalmologic abnormalities, large and late-closing fontanel, joint hyperlaxity, athetoid movements, hyperreflexia, growth retardation, intellectual deficit, developmental delay, corneal clouding, and cataract.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070143", 
        "name": "autosomal recessive cutis laxa type III"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070143#disease-associations", 
            "id": "0070143", 
            "database": "Alliance of Genome Resources"
        }
    ]
}