{
    "disease_id": "DOID:0111150", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007514", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007514", 
            "name": "ectopia lentis 1, isolated, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007514", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007514", 
            "name": "ectopia lentis 1, isolated, autosomal dominant; ECTOL1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007514", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007514", 
            "name": "isolated ectopia lentis caused by mutation in FBN1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007514", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007514", 
            "name": "FBN1 isolated ectopia lentis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007514", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007514", 
            "name": "ECTOL1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111150", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111150", 
            "name": "ECTOL1"
        }, 
        {
            "url": "https://www.omim.org/entry/129600", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:129600", 
            "name": "Ectopia lentis 1, isolated, autosomal dominant"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111150", 
        "description": "An isolated ectopia lentis that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111150", 
        "name": "autosomal dominant isolated ectopia lentis 1"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/129600", 
            "id": "129600", 
            "database": "MIM"
        }
    ]
}