{
    "disease_id": "DOID:0110281", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011170", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011170", 
            "name": "LGMD2G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011170", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011170", 
            "name": "autosomal recessive limb-girdle muscular dystrophy caused by mutation in TCAP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011170", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011170", 
            "name": "muscular dystrophy, limb-girdle, type 2G; LGMD2G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011170", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011170", 
            "name": "limb-girdle muscular dystrophy, type 2G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011170", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011170", 
            "name": "muscular dystrophy, limb-girdle, type 2G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011170", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011170", 
            "name": "TCAP autosomal recessive limb-girdle muscular dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011170", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011170", 
            "name": "limb-girdle muscular dystrophy due to telethonin deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110281", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110281", 
            "name": "LGMD2G"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110281", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110281", 
            "name": "muscular dystrophy, limb-girdle, type 2G"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110281", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110281", 
            "name": "limb-girdle muscular dystrophy due to telethonin deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110281", 
        "description": "An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in mutation in the gene encoding telethonin (TCAP).", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110281", 
        "name": "autosomal recessive limb-girdle muscular dystrophy type 2G"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110281#disease-associations", 
            "id": "0110281", 
            "database": "Alliance of Genome Resources"
        }
    ]
}