{
    "disease_id": "DOID:0110285", 
    "crossref_internal": {
        "protein": [
            "Q15149-1"
        ]
    }, 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013390", 
            "resource": "MONDO", 
            "description": "", 
            "name": "muscular dystrophy, limb-girdle, type 2Q; LGMD2Q", 
            "id": "MONDO:0013390"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013390", 
            "resource": "MONDO", 
            "description": "", 
            "name": "limb-girdle muscular dystrophy type 2Q", 
            "id": "MONDO:0013390"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013390", 
            "resource": "MONDO", 
            "description": "", 
            "name": "muscular dystrophy, limb-girdle, type 2Q", 
            "id": "MONDO:0013390"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013390", 
            "resource": "MONDO", 
            "description": "", 
            "name": "LGMD2Q", 
            "id": "MONDO:0013390"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013390", 
            "resource": "MONDO", 
            "description": "", 
            "name": "autosomal recessive limb-girdle muscular dystrophy due to plectin deficiency", 
            "id": "MONDO:0013390"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110285", 
            "resource": "Disease Ontology", 
            "description": "", 
            "name": "LGMD2Q", 
            "id": "DOID:0110285"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110285", 
            "resource": "Disease Ontology", 
            "description": "", 
            "name": "muscular dystrophy, limb-girdle, type 2Q", 
            "id": "DOID:0110285"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110285", 
            "resource": "Disease Ontology", 
            "description": "", 
            "name": "autosomal recessive limb-girdle muscular dystrophy due to plectin deficiency", 
            "id": "DOID:0110285"
        }, 
        {
            "url": "https://www.omim.org/entry/613723", 
            "resource": "MIM", 
            "description": "", 
            "name": "Muscular dystrophy, limb-girdle, autosomal recessive 17", 
            "id": "MIM:613723"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110285", 
        "resource": "Disease Ontology", 
        "description": "An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the PLEC1 gene.", 
        "name": "autosomal recessive limb-girdle muscular dystrophy type 2Q", 
        "id": "DOID:0110285"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613723", 
            "id": "613723", 
            "database": "MIM"
        }
    ]
}