{
    "disease_id": "DOID:0080675", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011493", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011493", 
            "name": "Stickler syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011493", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011493", 
            "name": "Stickler syndrome, vitreous type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011493", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011493", 
            "name": "Stickler syndrome caused by mutation in COL11A1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011493", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011493", 
            "name": "Stickler syndrome type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011493", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011493", 
            "name": "STICKLER syndrome, type II; STL2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011493", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011493", 
            "name": "STL 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011493", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011493", 
            "name": "STICKLER syndrome, type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011493", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011493", 
            "name": "Stickler syndrome, beaded vitreous type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011493", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011493", 
            "name": "STL2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011493", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011493", 
            "name": "Stickler syndrome, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011493", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011493", 
            "name": "COL11A1 Stickler syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080675", 
        "description": "A Stickler syndrome that has_material_basis_in heterozygous mutation in the COL11A1 gene on chromosome 1p21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080675", 
        "name": "Stickler syndrome 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080675#disease-associations", 
            "id": "0080675", 
            "database": "Alliance of Genome Resources"
        }
    ]
}