{
    "disease_id": "DOID:0080026", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0044206", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0044206", 
            "name": "Nance-Insley syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0044206", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0044206", 
            "name": "OSMEDB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0044206", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0044206", 
            "name": "chondrodystrophy with sensorineural deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0044206", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0044206", 
            "name": "Nance-Sweeney chondrodysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0044206", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0044206", 
            "name": "OSMED"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0044206", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0044206", 
            "name": "otospondylomegaepiphyseal dysplasia, autosomal recessive; OSMEDB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0044206", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0044206", 
            "name": "Weissenbacher-Zweymuller syndrome, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0044206", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0044206", 
            "name": "Weissenbacher-Zweymuller syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080026", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080026", 
            "name": "OSMEDB"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080026", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080026", 
            "name": "CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080026", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080026", 
            "name": "NANCE-INSLEY SYNDROME"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080026", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080026", 
            "name": "NANCE-SWEENEY CHONDRODYSPLASIA"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080026", 
        "description": "An osteochondrodysplasia that results from mutations autosomal recessive inheritance of mutations in the COL11A2 gene which results_in enlargement of the located_in epiphysis in located_in hand and located_in foot, distinct facial features, platyspondyly and hearing loss.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080026", 
        "name": "otospondylomegaepiphyseal dysplasia, autosomal recessive"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/215150", 
            "id": "215150", 
            "database": "MIM"
        }
    ]
}