{
    "disease_id": "DOID:0110293", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013440", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013440", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013440", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013440", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013440", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013440", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013440", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013440", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013440", 
            "name": "autosomal recessive limb-girdle muscular dystrophy caused by mutation in DAG1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013440", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013440", 
            "name": "muscular dystrophy-dystroglycanopathy, limb-girdle, Dag1-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013440", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013440", 
            "name": "muscular dystrophy, limb-girdle, type 2P"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013440", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013440", 
            "name": "LGMD2P"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110293", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110293", 
            "name": "LGMD2P"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110293", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110293", 
            "name": "MDDGC9"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110293", 
            "name": "muscular dystrophy-dystroglycanopathy (limb-girdle) type C9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110293", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110293", 
            "name": "muscular dystrophy-dystroglycanopathy limb-girdle DAG1-related"
        }, 
        {
            "url": "https://www.omim.org/entry/613818", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:613818", 
            "name": "Muscular dystrophy-dystroglycanopathy limb-girdle C9"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110293", 
        "description": "An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the gene encoding alpha-dystroglycan (DAG1) on chromosome 3p21.", 
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        "id": "DOID:0110293", 
        "name": "autosomal recessive limb-girdle muscular dystrophy type 2P"
    }, 
    "evidence": [
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            "id": "613818", 
            "database": "MIM"
        }
    ]
}