{
    "disease_id": "DOID:0070266",
    "recommended_name": {
        "id": "DOID:0070266",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070266",
        "name": "congenital disorder of glycosylation type IIn",
        "description": "A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of the SLC39A8 gene on chromosome 4q24."
    },
    "synonyms": [
        {
            "id": "DOID:0070266",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070266",
            "name": "Carbohydrate deficient glycoprotein syndrome type IIn",
            "description": ""
        },
        {
            "id": "DOID:0070266",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070266",
            "name": "CDG IIn",
            "description": ""
        },
        {
            "id": "DOID:0070266",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070266",
            "name": "CDG syndrome type IIn",
            "description": ""
        },
        {
            "id": "DOID:0070266",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070266",
            "name": "CDG2N",
            "description": ""
        },
        {
            "id": "DOID:0070266",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070266",
            "name": "Congenital disorder of glycosylation type 2n",
            "description": ""
        },
        {
            "id": "DOID:0070266",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070266",
            "name": "SLC39A8-CDG",
            "description": ""
        },
        {
            "id": "DOID:0070266",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070266",
            "name": "CDGIIn",
            "description": ""
        },
        {
            "id": "MONDO:0014746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014746",
            "name": "SLC39A8-CDG",
            "description": ""
        },
        {
            "id": "MONDO:0014746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014746",
            "name": "CDG syndrome type IIn",
            "description": ""
        },
        {
            "id": "MONDO:0014746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014746",
            "name": "CDG-IIn",
            "description": ""
        },
        {
            "id": "MONDO:0014746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014746",
            "name": "CDG2N",
            "description": ""
        },
        {
            "id": "MONDO:0014746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014746",
            "name": "SLC39A8 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0014746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014746",
            "name": "carbohydrate deficient glycoprotein syndrome type IIn",
            "description": ""
        },
        {
            "id": "MONDO:0014746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014746",
            "name": "congenital disorder of glycosylation type 2n",
            "description": ""
        },
        {
            "id": "MONDO:0014746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014746",
            "name": "congenital disorder of glycosylation type IIn",
            "description": ""
        },
        {
            "id": "MONDO:0014746",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014746",
            "name": "congenital disorder of glycosylation, type IIn",
            "description": ""
        },
        {
            "id": "MIM:616721",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616721",
            "name": "Congenital disorder of glycosylation 2N",
            "description": "Congenital disorder of glycosylation 2N"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070266"
    ],
    "unlinked_id_list": []
}