{
    "disease_id": "DOID:0070247", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021569", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021569", 
            "name": "Emery-Dreifuss muscular dystrophy 2, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021569", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021569", 
            "name": "scapuloilioperoneal atrophy with cardiopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021569", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021569", 
            "name": "Emery-Dreifuss muscular dystrophy, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021569", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021569", 
            "name": "EMD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021569", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021569", 
            "name": "Hauptmann-Thannhauser muscular dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021569", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021569", 
            "name": "EDMD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021569", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021569", 
            "name": "muscular dystrophy with early contractures and cardiomyopathy, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021569", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021569", 
            "name": "Emery-Dreifuss muscular dystrophy 2, autosomal dominant; EDMD2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070247", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070247", 
            "name": "muscular dystrophy with early contractures and cardiomyopathy, autosomal dominant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070247", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070247", 
            "name": "EDMD2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070247", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070247", 
            "name": "EMD2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070247", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070247", 
            "name": "Hauptmann-Thannhauser muscular dystrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070247", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070247", 
            "name": "scapuloilioperoneal atrophy with cardiopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070247", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070247", 
            "name": "Emery-Dreifuss muscular dystrophy 2, autosomal dominant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070247", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070247", 
            "name": "Emery-Dreifuss muscular dystrophy, autosomal dominant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070247", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070247", 
            "name": "autosomal dominant limb-girdle muscular dystrophy type 1B"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070247", 
        "description": "An Emery-Dreifuss muscular dystrophy that has_material_basis_in an autosomal dominant mutation of LMNA on chromosome 1q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070247", 
        "name": "autosomal dominant Emery-Dreifuss muscular dystrophy 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070247#disease-associations", 
            "id": "0070247", 
            "database": "Alliance of Genome Resources"
        }
    ]
}