{
    "disease_id": "DOID:0110274", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009675", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009675", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009675", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009675", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009675", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009675", 
            "name": "limb-girdle muscular dystrophy type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009675", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009675", 
            "name": "myositis, eosinophilic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009675", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009675", 
            "name": "calpainopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009675", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009675", 
            "name": "muscular dystrophy, Pelvofemoral"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009675", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009675", 
            "name": "muscular dystrophy limb girdle type 2A, erb type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009675", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009675", 
            "name": "Leyden-Moebius muscular dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009675", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009675", 
            "name": "limb-girdle muscular dystrophy due to calpain deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009675", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009675", 
            "name": "muscular dystrophy, limb-girdle, type 2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009675", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009675", 
            "name": "CAPN3 autosomal recessive limb-girdle muscular dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009675", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009675", 
            "name": "LGMD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009675", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009675", 
            "name": "LGMD2A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009675", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009675", 
            "name": "pelvofemoral muscular dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009675", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009675", 
            "name": "autosomal recessive limb-girdle muscular dystrophy caused by mutation in CAPN3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009675", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009675", 
            "name": "muscular dystrophy, limb-girdle, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009675", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009675", 
            "name": "primary calpainopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009675", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009675", 
            "name": "limb-girdle muscular dystrophy type 2A"
        }, 
        {
            "url": "https://www.omim.org/entry/253600", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:253600", 
            "name": "Muscular dystrophy, limb-girdle, autosomal recessive 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110274", 
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        "resource": "Disease Ontology", 
        "id": "DOID:0110274", 
        "name": "autosomal recessive limb-girdle muscular dystrophy"
    }, 
    "evidence": [
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            "id": "253600", 
            "database": "MIM"
        }
    ]
}