{
    "disease_id": "DOID:0110299", 
    "synonyms": [
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            "description": "", 
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            "description": "", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011787", 
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            "description": "", 
            "resource": "MONDO", 
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            "description": "", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011787", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011787", 
            "name": "limb-girdle muscular dystrophy type 2I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011787", 
            "name": "muscular dystrophy-dystroglycanopathy (limb-girdle) type C 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011787", 
            "name": "muscular dystrophy-dystroglycanopathy limb-girdle FRKP-related"
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        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011787", 
            "name": "muscular dystrophy limb-girdle type 2I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011787", 
            "name": "muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5; MDDGC5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011787", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011787", 
            "name": "autosomal recessive limb-girdle muscular dystrophy caused by mutation in FKRP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011787", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011787", 
            "name": "muscular dystrophy, limb-girdle, type 2I"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110299", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110299", 
            "name": "LGMD2I"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110299", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110299", 
            "name": "MDDGC5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110299", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110299", 
            "name": "muscular dystrophy limb-girdle type 2I"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110299", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110299", 
            "name": "muscular dystrophy-dystroglycanopathy limb-girdle FRKP-related"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110299", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110299", 
            "name": "Limb-girdle muscular dystrophy due to FKRP deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110299", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110299", 
            "name": "muscular dystrophy-dystroglycanopathy (limb-girdle) type C 5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110299", 
        "description": "An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding fukutin-related protein (FKRP) on chromosome 19q13.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110299", 
        "name": "autosomal recessive limb-girdle muscular dystrophy type 2I"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110299#disease-associations", 
            "id": "0110299", 
            "database": "Alliance of Genome Resources"
        }
    ]
}