{
    "disease_id": "DOID:0110294", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014142", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014142", 
            "name": "LGMD2T"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014142", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014142", 
            "name": "muscular dystrophy-dystroglycanopathy limb-girdle GMPPB-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014142", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014142", 
            "name": "muscular dystrophy, limb-girdle, type 2T"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014142", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014142", 
            "name": "muscular dystrophy-dystroglycanopathy (limb-girdle) type C14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014142", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014142", 
            "name": "muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014142", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014142", 
            "name": "autosomal recessive limb-girdle muscular dystrophy caused by mutation in GMPPB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014142", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014142", 
            "name": "muscular dystrophy limb-girdle type 2T"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014142", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014142", 
            "name": "GMPPB autosomal recessive limb-girdle muscular dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014142", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014142", 
            "name": "limb-girdle muscular dystrophy type 2T"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014142", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014142", 
            "name": "muscular dystrophy-dystroglycanopathy, limb-girdle, GMPPB-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014142", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014142", 
            "name": "muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14; MDDGC14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014142", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014142", 
            "name": "MDDGC14"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110294", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110294", 
            "name": "LGMD2T"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110294", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110294", 
            "name": "MDDGC14"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110294", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110294", 
            "name": "muscular dystrophy limb-girdle type 2T"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110294", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110294", 
            "name": "muscular dystrophy-dystroglycanopathy (limb-girdle) type C14"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110294", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110294", 
            "name": "muscular dystrophy-dystroglycanopathy limb-girdle GMPPB-related"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110294", 
        "description": "An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the GMPPB gene encoding the beta subunit of GDP-mannose pyrophosphorylase on chromosome 3p21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110294", 
        "name": "autosomal recessive limb-girdle muscular dystrophy type 2T"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110294#disease-associations", 
            "id": "0110294", 
            "database": "Alliance of Genome Resources"
        }
    ]
}