{
    "disease_id": "DOID:0070269",
    "recommended_name": {
        "id": "DOID:0070269",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070269",
        "name": "congenital disorder of glycosylation type IIq",
        "description": "A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of the COG2 gene on chromosome 1q42.2."
    },
    "synonyms": [
        {
            "id": "DOID:0070269",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070269",
            "name": "CDG IIq",
            "description": ""
        },
        {
            "id": "DOID:0070269",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070269",
            "name": "CDG2Q",
            "description": ""
        },
        {
            "id": "DOID:0070269",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070269",
            "name": "COG2-CDG",
            "description": ""
        },
        {
            "id": "DOID:0070269",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070269",
            "name": "COG2-related congenital disorder of glycosylation",
            "description": ""
        },
        {
            "id": "DOID:0070269",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070269",
            "name": "CDGIIq",
            "description": ""
        },
        {
            "id": "MONDO:0054559",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054559",
            "name": "congenital disorder of glycosylation, type IIq",
            "description": ""
        },
        {
            "id": "MONDO:0054559",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054559",
            "name": "COG2-CDG",
            "description": ""
        },
        {
            "id": "MONDO:0054559",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054559",
            "name": "COG2-related congenital disorder of glycosylation",
            "description": ""
        },
        {
            "id": "MONDO:0054559",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054559",
            "name": "CDG Iiq",
            "description": ""
        },
        {
            "id": "MONDO:0054559",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054559",
            "name": "CDG2Q",
            "description": ""
        },
        {
            "id": "MIM:617395",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617395",
            "name": "Congenital disorder of glycosylation 2Q",
            "description": "Congenital disorder of glycosylation 2Q"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070269"
    ],
    "unlinked_id_list": []
}