{
    "disease_id": "DOID:0080677", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008490", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008490", 
            "name": "Stickler syndrome type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008490", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008490", 
            "name": "Pierre Robin syndrome with fetal chondrodysplasia Stickler syndrome, Nonocular type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008490", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008490", 
            "name": "Stickler syndrome, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008490", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008490", 
            "name": "STICKLER syndrome, type III; STL3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008490", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008490", 
            "name": "Stickler syndrome nonocular type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008490", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008490", 
            "name": "OSMED, heterozygous"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008490", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008490", 
            "name": "STICKLER syndrome, type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008490", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008490", 
            "name": "OSMEDA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008490", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008490", 
            "name": "otospondylomegaepiphyseal dysplasia, autosomal dominant; OSMEDA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008490", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008490", 
            "name": "COL11A2 Stickler syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008490", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008490", 
            "name": "STL3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008490", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008490", 
            "name": "Stickler syndrome, non-ocular type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008490", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008490", 
            "name": "Stickler syndrome caused by mutation in COL11A2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008490", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008490", 
            "name": "Stickler syndrome, type III, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008490", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008490", 
            "name": "Pierre Robin syndrome with fetal chondrodysplasia Stickler syndrome, Nonocular type, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008490", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008490", 
            "name": "Stickler syndrome, Nonocular type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080677", 
        "description": "An osteochondrodysplasia that is characterized by by autosomal dominant inheritance of mutations in the COL11A2 gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080677", 
        "name": "otospondylomegaepiphyseal dysplasia, autosomal dominant"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/184840", 
            "id": "184840", 
            "database": "MIM"
        }
    ]
}