{
    "disease_id": "DOID:0110292", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013161", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013161", 
            "name": "LGMD2O"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013161", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013161", 
            "name": "muscular dystrophy, limb-girdle, type 2O"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013161", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013161", 
            "name": "autosomal recessive limb-girdle muscular dystrophy caused by mutation in POMGNT1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013161", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013161", 
            "name": "POMGNT1 autosomal recessive limb-girdle muscular dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013161", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013161", 
            "name": "muscular dystrophy-dystroglycanopathy (limb-girdle) type C3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013161", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013161", 
            "name": "muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3; MDDGC3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013161", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013161", 
            "name": "MDDGC3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013161", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013161", 
            "name": "muscular dystrophy-dystroglycanopathy limb-girdle POMGNT1-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013161", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013161", 
            "name": "muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013161", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013161", 
            "name": "muscular dystrophy-dystroglycanopathy, limb-girdle, POMGNT1-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013161", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013161", 
            "name": "limb-girdle muscular dystrophy type 2O"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110292", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110292", 
            "name": "muscular dystrophy-dystroglycanopathy limb-girdle POMGNT1-related"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110292", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110292", 
            "name": "LGMD2O"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110292", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110292", 
            "name": "MDDGC3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110292", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110292", 
            "name": "muscular dystrophy-dystroglycanopathy (limb-girdle) type C3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110292", 
        "description": "An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the gene encoding protein O-mannose beta-1,2-N-acetylglucosaminyltransferase (POMGNT1) on chromosome 1p34.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110292", 
        "name": "autosomal recessive limb-girdle muscular dystrophy type 2O"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110292#disease-associations", 
            "id": "0110292", 
            "database": "Alliance of Genome Resources"
        }
    ]
}