{
    "disease_id": "DOID:0070267", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014789", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014789", 
            "name": "CCDC115-CDG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014789", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014789", 
            "name": "CDG syndrome type IIo"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014789", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014789", 
            "name": "congenital disorder of glycosylation type 2o"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014789", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014789", 
            "name": "congenital disorder of glycosylation, type IIo"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014789", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014789", 
            "name": "CDG2O"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014789", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014789", 
            "name": "carbohydrate deficient glycoprotein syndrome type IIo"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014789", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014789", 
            "name": "CDG-IIo"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014789", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014789", 
            "name": "congenital disorder of glycosylation, type IIo; CDG2O"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014789", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014789", 
            "name": "CDG IIo"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070267", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070267", 
            "name": "Carbohydrate deficient glycoprotein syndrome type IIo"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070267", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070267", 
            "name": "CCDC115-CDG"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070267", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070267", 
            "name": "CDG IIo"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070267", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070267", 
            "name": "CDG syndrome type IIo"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070267", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070267", 
            "name": "CDG2O"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070267", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070267", 
            "name": "CDGIIdo"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070267", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070267", 
            "name": "Congenital disorder of glycosylation type 2o"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070267", 
        "description": "A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of CCDC115 on chromosome 2q21.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070267", 
        "name": "congenital disorder of glycosylation type IIo"
    }, 
    "evidence": [
        {
            "url": "https://panelapp.genomicsengland.co.uk/panels/25/gene/CCDC115/#!details", 
            "id": "CCDC115", 
            "database": "Genomics England"
        }
    ]
}