{
    "disease_id": "DOID:0070261",
    "recommended_name": {
        "id": "DOID:0070261",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070261",
        "name": "congenital disorder of glycosylation type IIi",
        "description": "A congenital disorder of glycosylation type II that has_material_basis_in a mutation of the COG5 gene on chromosome 7q22.3."
    },
    "synonyms": [
        {
            "id": "DOID:0070261",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070261",
            "name": "Carbohydrate deficient glycoprotein syndrome type IIi",
            "description": ""
        },
        {
            "id": "DOID:0070261",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070261",
            "name": "CDG IIi",
            "description": ""
        },
        {
            "id": "DOID:0070261",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070261",
            "name": "CDG syndrome type IIi",
            "description": ""
        },
        {
            "id": "DOID:0070261",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070261",
            "name": "CDG2I",
            "description": ""
        },
        {
            "id": "DOID:0070261",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070261",
            "name": "COG5-CDG",
            "description": ""
        },
        {
            "id": "DOID:0070261",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070261",
            "name": "Congenital disorder of glycosylation type 2i",
            "description": ""
        },
        {
            "id": "DOID:0070261",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070261",
            "name": "CDGIIi",
            "description": ""
        },
        {
            "id": "MONDO:0013325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013325",
            "name": "COG5-congenital disorder of glycosylation",
            "description": "COG5-CDG is an extremely rare form of CDG syndrome characterized clinically in the single reported case to date by moderate mental retardation with slow and inarticulate speech, truncal ataxia, and mild hypotonia."
        },
        {
            "id": "MONDO:0013325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013325",
            "name": "CDG syndrome type III",
            "description": ""
        },
        {
            "id": "MONDO:0013325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013325",
            "name": "CDG-III",
            "description": ""
        },
        {
            "id": "MONDO:0013325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013325",
            "name": "CDG2I",
            "description": ""
        },
        {
            "id": "MONDO:0013325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013325",
            "name": "COG5-CDG",
            "description": ""
        },
        {
            "id": "MONDO:0013325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013325",
            "name": "COG5-congenital disorder of glycosylation",
            "description": ""
        },
        {
            "id": "MONDO:0013325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013325",
            "name": "carbohydrate deficient glycoprotein syndrome type III",
            "description": ""
        },
        {
            "id": "MONDO:0013325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013325",
            "name": "congenital disorder of glycosylation type 2i",
            "description": ""
        },
        {
            "id": "MONDO:0013325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013325",
            "name": "congenital disorder of glycosylation type III",
            "description": ""
        },
        {
            "id": "MONDO:0013325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013325",
            "name": "CDG syndrome type 3",
            "description": ""
        },
        {
            "id": "MONDO:0013325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013325",
            "name": "COG5-CDG (CDG-III)",
            "description": ""
        },
        {
            "id": "MONDO:0013325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013325",
            "name": "congenital disorder of glycosylation, type III",
            "description": ""
        },
        {
            "id": "MIM:613612",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613612",
            "name": "Congenital disorder of glycosylation 2I",
            "description": "Congenital disorder of glycosylation 2I"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070261"
    ],
    "unlinked_id_list": []
}