{
    "disease_id": "DOID:0110295", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014474", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014474", 
            "name": "muscular dystrophy limb-girdle type 2U"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014474", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014474", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014474", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014474", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014474", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014474", 
            "name": "LGMD2U"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014474", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014474", 
            "name": "muscular dystrophy, limb-girdle, type 2U"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014474", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014474", 
            "name": "autosomal recessive limb-girdle muscular dystrophy caused by mutation in ISPD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014474", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014474", 
            "name": "muscular dystrophy-dystroglycanopathy (limb-girdle) type C7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014474", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014474", 
            "name": "muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7; MDDGC7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014474", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014474", 
            "name": "autosomal recessive limb-girdle muscular dystrophy due to ISPD deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110295", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110295", 
            "name": "autosomal recessive limb-girdle muscular dystrophy due to ISPD deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110295", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110295", 
            "name": "LGMD2U"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110295", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110295", 
            "name": "MDDGC7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110295", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110295", 
            "name": "muscular dystrophy limb-girdle type 2U"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110295", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110295", 
            "name": "muscular dystrophy-dystroglycanopathy (limb-girdle) type C7"
        }, 
        {
            "url": "https://www.omim.org/entry/616052", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:616052", 
            "name": "Muscular dystrophy-dystroglycanopathy limb-girdle C7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110295", 
        "description": "An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the ISPD gene on chromosome 7p21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110295", 
        "name": "autosomal recessive limb-girdle muscular dystrophy type 2U"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616052", 
            "id": "616052", 
            "database": "MIM"
        }
    ]
}