{
    "disease_id": "DOID:0110306", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012193", 
            "name": "autosomal dominant limb-girdle muscular dystrophy type 1G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012193", 
            "name": "HNRNPDL autosomal dominant limb-girdle muscular dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012193", 
            "name": "autosomal dominant limb-girdle muscular dystrophy caused by mutation in HNRNPDL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012193", 
            "name": "muscular dystrophy limb-girdle type 1G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012193", 
            "name": "limb-girdle muscular dystrophy, type 1G; LGMD1G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012193", 
            "name": "limb-girdle muscular dystrophy, type 1G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012193", 
            "name": "limb-girdle muscular dystrophy type 1G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012193", 
            "name": "LGMD1G"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110306", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110306", 
            "name": "LGMD1G"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110306", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110306", 
            "name": "autosomal dominant limb-girdle muscular dystrophy type 1G"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110306", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110306", 
            "name": "muscular dystrophy limb-girdle type 1G"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110306", 
        "description": "An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in heterozygous mutation in the HNRNPDL gene on chromosome 4q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110306", 
        "name": "autosomal dominant limb-girdle muscular dystrophy type 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110306#disease-associations", 
            "id": "0110306", 
            "database": "Alliance of Genome Resources"
        }
    ]
}