{
    "disease_id": "DOID:0110282", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009683", 
            "name": "LGMD2H"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009683", 
            "name": "muscular dystrophy limb-girdle type 2H"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009683", 
            "name": "limb-girdle muscular dystrophy type 2H"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009683", 
            "name": "muscular dystrophy Hutterite type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009683", 
            "name": "muscular dystrophy, limb-girdle, type 2H; LGMD2H"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009683", 
            "name": "autosomal recessive limb-girdle muscular dystrophy caused by mutation in TRIM32"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009683", 
            "name": "sarcotubular myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009683", 
            "name": "muscular dystrophy, limb-girdle, type 2H"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009683", 
            "name": "muscular dystrophy, Hutterite type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009683", 
            "name": "TRIM32 autosomal recessive limb-girdle muscular dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009683", 
            "name": "limb-girdle muscular dystrophy due to TRIM32 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110282", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110282", 
            "name": "LGMD2H"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110282", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110282", 
            "name": "muscular dystrophy Hutterite type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110282", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110282", 
            "name": "sarcotubular myopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110282", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110282", 
            "name": "limb-girdle muscular dystrophy due to TRIM32 deficiency"
        }, 
        {
            "url": "https://www.omim.org/entry/254110", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:254110", 
            "name": "Muscular dystrophy, limb-girdle, autosomal recessive 8"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110282", 
        "description": "An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in mutation in the gene encoding tripartite motif-containing protein-32 (TRIM32) on chromosome 9q.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110282", 
        "name": "autosomal recessive limb-girdle muscular dystrophy type 2H"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/254110", 
            "id": "254110", 
            "database": "MIM"
        }
    ]
}