{
    "disease_id": "DOID:0110290", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014782", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014782", 
            "name": "BVES autosomal recessive limb-girdle muscular dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014782", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014782", 
            "name": "muscular dystrophy, limb-girdle, type 2X"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014782", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014782", 
            "name": "autosomal recessive limb-girdle muscular dystrophy-cardiac arrhythmia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014782", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014782", 
            "name": "muscular dystrophy, limb-girdle, type 2X; LGMD2X"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014782", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014782", 
            "name": "LGMD2X"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014782", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014782", 
            "name": "autosomal recessive limb-girdle muscular dystrophy caused by mutation in BVES"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110290", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110290", 
            "name": "LGMD2X"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110290", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110290", 
            "name": "muscular dystrophy, limb-girdle, type 2X"
        }, 
        {
            "url": "https://www.omim.org/entry/616812", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:616812", 
            "name": "Muscular dystrophy, limb-girdle, autosomal recessive 25"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110290", 
        "description": "An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the BVES gene on chromosome 6q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110290", 
        "name": "autosomal recessive limb-girdle muscular dystrophy type 2X"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616812", 
            "id": "616812", 
            "database": "MIM"
        }
    ]
}