{
    "disease_id": "DOID:0110637", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012138", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012138", 
            "name": "MDDGB6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012138", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012138", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012138", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012138", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6; MDDGB6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012138", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012138", 
            "name": "congenital muscular dystrophy large-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012138", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012138", 
            "name": "congenital muscular dystrophy type 1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012138", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012138", 
            "name": "muscular dystrophy, congenital, type 1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012138", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012138", 
            "name": "muscular dystrophy, congenital, large-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012138", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012138", 
            "name": "MDC1D"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110637", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110637", 
            "name": "MDC1D"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110637", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110637", 
            "name": "MDDGB6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110637", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110637", 
            "name": "congenital muscular dystrophy LARGE-related"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110637", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110637", 
            "name": "congenital muscular dystrophy type 1D"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110637", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110637", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110637", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110637", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110637", 
        "description": "A congenital muscular dystrophy characterized by autosomal recessive inheritance of muscular dystrophy with mental retardation and structural brain abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the LARGE gene on chromosome 22q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110637", 
        "name": "muscular dystrophy-dystroglycanopathy type B6"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110637#disease-associations", 
            "id": "0110637", 
            "database": "Alliance of Genome Resources"
        }
    ]
}