{
    "disease_id": "DOID:0070261",
    "recommended_name": {
        "id": "DOID:0070261",
        "resource": "Disease Ontology",
        "url": "http://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 COG5 on chromosome 7q22.3."
    },
    "synonyms": [
        {
            "id": "DOID:0070261",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070261",
            "name": "Carbohydrate deficient glycoprotein syndrome type IIi",
            "description": ""
        },
        {
            "id": "DOID:0070261",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070261",
            "name": "CDG IIi",
            "description": ""
        },
        {
            "id": "DOID:0070261",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070261",
            "name": "CDG syndrome type IIi",
            "description": ""
        },
        {
            "id": "DOID:0070261",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070261",
            "name": "CDG2I",
            "description": ""
        },
        {
            "id": "DOID:0070261",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070261",
            "name": "CDGIIdi",
            "description": ""
        },
        {
            "id": "DOID:0070261",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070261",
            "name": "COG5-CDG",
            "description": ""
        },
        {
            "id": "DOID:0070261",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070261",
            "name": "Congenital disorder of glycosylation type 2i",
            "description": ""
        },
        {
            "id": "MONDO:0013325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013325",
            "name": "COG5-CDG",
            "description": "COG5-CDG is an extremely rare form of CDG syndrome (see this term) 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 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": "congenital disorder of glycosylation type III",
            "description": ""
        },
        {
            "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": "congenital disorder of glycosylation, 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": "CDG syndrome type 3",
            "description": ""
        },
        {
            "id": "MONDO:0013325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013325",
            "name": "congenital disorder of glycosylation, type III; CDG2I",
            "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": "CDG-III",
            "description": ""
        },
        {
            "id": "MONDO:0013325",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013325",
            "name": "COG5-CDG (CDG-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"
        }
    ]
}