{
    "disease_id": "DOID:0110288", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014788", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014788", 
            "name": "muscular dystrophy, limb-girdle, type 2W"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014788", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014788", 
            "name": "LGMD2W"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014788", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014788", 
            "name": "LIMS2 autosomal recessive limb-girdle muscular dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014788", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014788", 
            "name": "muscular dystrophy, limb-girdle, type 2W; LGMD2W"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014788", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014788", 
            "name": "autosomal recessive limb-girdle muscular dystrophy caused by mutation in LIMS2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110288", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110288", 
            "name": "LGMD2W"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110288", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110288", 
            "name": "muscular dystrophy, limb-girdle, type 2W"
        }, 
        {
            "url": "https://www.omim.org/entry/616827", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:616827", 
            "name": "Muscular dystrophy, autosomal recessive, with cardiomyopathy and triangular tongue"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110288", 
        "description": "An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in compound heterozygous mutation in the LIM zinc finger domain containing 2 gene (LIMS2) on chromosome 2q14.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110288", 
        "name": "autosomal recessive limb-girdle muscular dystrophy type 2W"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616827", 
            "id": "616827", 
            "database": "MIM"
        }
    ]
}