{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013325", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013325", 
            "name": "COG5-CDG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013325", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013325", 
            "name": "CDG III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013325", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013325", 
            "name": "CDG2I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013325", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013325", 
            "name": "CDG syndrome type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013325", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013325", 
            "name": "congenital disorder of glycosylation, type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013325", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013325", 
            "name": "congenital disorder of glycosylation type 2i"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013325", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013325", 
            "name": "CDG syndrome type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013325", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013325", 
            "name": "congenital disorder of glycosylation, type III; CDG2I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013325", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013325", 
            "name": "carbohydrate deficient glycoprotein syndrome type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013325", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013325", 
            "name": "CDG-III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013325", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013325", 
            "name": "COG5-CDG (CDG-III)"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070261", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070261", 
            "name": "Carbohydrate deficient glycoprotein syndrome type IIi"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070261", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070261", 
            "name": "CDG IIi"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070261", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070261", 
            "name": "CDG syndrome type IIi"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070261", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070261", 
            "name": "CDG2I"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070261", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070261", 
            "name": "CDGIIdi"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070261", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070261", 
            "name": "COG5-CDG"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070261", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070261", 
            "name": "Congenital disorder of glycosylation type 2i"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070261", 
        "description": "A congenital disorder of glycosylation type II that has_material_basis_in a mutation of COG5 on chromosome 7q22.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070261", 
        "name": "congenital disorder of glycosylation type IIi"
    }, 
    "evidence": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013325", 
            "id": "0013325", 
            "database": "MONDO"
        }, 
        {
            "url": "https://www.omim.org/entry/613612", 
            "id": "613612", 
            "database": "MIM"
        }, 
        {
            "url": "https://panelapp.genomicsengland.co.uk/panels/25/gene/COG5/#!details", 
            "id": "COG5", 
            "database": "Genomics England"
        }
    ]
}