{
    "disease_id": "DOID:11723", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010679", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010679", 
            "name": "muscular dystrophy, Duchenne type; DMD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010679", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010679", 
            "name": "DMD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010679", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010679", 
            "name": "muscular dystrophy, Duchenne"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010679", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010679", 
            "name": "muscular dystrophy, pseudohypertrophic progressive, Duchenne type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010679", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010679", 
            "name": "muscular dystrophy, Duchenne type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010679", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010679", 
            "name": "severe dystrophinopathy, Duchenne type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:11723", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:11723", 
            "name": "Muscular dystrophy, Duchenne"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:11723", 
        "description": "A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy.", 
        "resource": "Disease Ontology", 
        "id": "DOID:11723", 
        "name": "Duchenne muscular dystrophy"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/11723#disease-associations", 
            "id": "11723", 
            "database": "Alliance of Genome Resources"
        }
    ]
}