{
    "disease_id": "DOID:0050759", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011266", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011266", 
            "name": "CNBP myotonic dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011266", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011266", 
            "name": "myotonic myopathy, proximal"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011266", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011266", 
            "name": "dystrophia myotonica type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011266", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011266", 
            "name": "myotonic dystrophy 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011266", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011266", 
            "name": "myotonic dystrophy caused by mutation in CNBP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011266", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011266", 
            "name": "DM2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011266", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011266", 
            "name": "proximal myotonic dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011266", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011266", 
            "name": "proximal myotonic myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011266", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011266", 
            "name": "PROMM"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011266", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011266", 
            "name": "dystrophia myotonica 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011266", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011266", 
            "name": "ricker disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011266", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011266", 
            "name": "myotonic dystrophy 2; DM2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011266", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011266", 
            "name": "ricker syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050759", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050759", 
            "name": "proximal myotonic myopathy"
        }, 
        {
            "url": "https://www.omim.org/entry/602668", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:602668", 
            "name": "Dystrophia myotonica 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050759", 
        "description": "A myotonic disease that is characterized by myotonia and progressive, proximal muscle wasting and weakness affecting the skeletal and smooth muscles of the neck, shoulders, elbows and hips and has_material_basis_in the autosomal dominant inheritance of the CNBP (ZNF9) gene containing an expansion of a CCTG repeat in intron one.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050759", 
        "name": "myotonic dystrophy type 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/602668", 
            "id": "602668", 
            "database": "MIM"
        }
    ]
}