{
    "disease_id": "DOID:0080676", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007160", 
            "name": "Stickler syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007160", 
            "name": "Stickler syndrome, type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007160", 
            "name": "Stickler syndrome, type I; STL1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007160", 
            "name": "Stickler syndrome, membranous vitreous type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007160", 
            "name": "Stickler syndrome, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007160", 
            "name": "Stickler syndrome, vitreous type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007160", 
            "name": "arthroophthalmopathy, hereditary progressive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007160", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007160", 
            "name": "STL1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080676", 
        "description": "A Stickler syndrome that has_material_basis_in heterozygous mutation in the COL2A1 gene on chromosome 12q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080676", 
        "name": "Stickler syndrome 1"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/108300", 
            "id": "108300", 
            "database": "MIM"
        }
    ]
}