{
    "disease_id": "DOID:0110286",
    "recommended_name": {
        "id": "DOID:0110286",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110286",
        "name": "obsolete autosomal recessive limb-girdle muscular dystrophy type 2R",
        "description": ""
    },
    "synonyms": [
        {
            "id": "MONDO:0014129",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014129",
            "name": "autosomal recessive limb-girdle muscular dystrophy type 2R",
            "description": "Autosomal recessive limb-girdle muscular dystrophy type 2R (LGMD2R) is a form of limb-girdle muscular dystrophy characterized by the adolescent or early adulthood-onset of progressive proximal muscle weakness and mild facial muscle weakness, with patients becoming wheelchair bound in their fourth to fifth decade of life. Mild, bilateral winged scapula, incomplete right bundle branch block, and a sinus rhythm with very rare ventricular extrasystoles have also been reported."
        },
        {
            "id": "MONDO:0014129",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014129",
            "name": "DES autosomal recessive limb-girdle muscular dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0014129",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014129",
            "name": "autosomal recessive limb-girdle muscular dystrophy caused by mutation in DES",
            "description": ""
        },
        {
            "id": "MONDO:0014129",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014129",
            "name": "muscular dystrophy, limb-girdle, type 2R; LGMD2R",
            "description": ""
        },
        {
            "id": "MONDO:0014129",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014129",
            "name": "autosomal recessive limb-girdle muscular dystrophy due to desmin deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0014129",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014129",
            "name": "LGMD2R",
            "description": ""
        },
        {
            "id": "MONDO:0014129",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014129",
            "name": "muscular dystrophy, limb-girdle, type 2R",
            "description": ""
        }
    ]
}