{
    "disease_id": "DOID:0070259",
    "recommended_name": {
        "id": "DOID:0070259",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070259",
        "name": "congenital disorder of glycosylation type IIg",
        "description": "A congenital disorder of glycosylation type II that has_material_basis_in a mutation of the COG1 gene on chromosome 17q25.1."
    },
    "synonyms": [
        {
            "id": "DOID:0070259",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070259",
            "name": "Carbohydrate deficient glycoprotein syndrome type IIg",
            "description": ""
        },
        {
            "id": "DOID:0070259",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070259",
            "name": "CDG IIg",
            "description": ""
        },
        {
            "id": "DOID:0070259",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070259",
            "name": "CDG2G",
            "description": ""
        },
        {
            "id": "DOID:0070259",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070259",
            "name": "CDGII/COG1 cerebrocostomandibular-like syndrome",
            "description": ""
        },
        {
            "id": "DOID:0070259",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070259",
            "name": "CDGIIg",
            "description": ""
        },
        {
            "id": "MONDO:0012637",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012637",
            "name": "COG1-congenital disorder of glycosylation",
            "description": "COG1-CDG is an extremely rare form of CDG syndrome characterized clinically in the few cases reported to date by variable signs including microcephaly, growth retardation, psychomotor retardation and facial dysmorphism."
        },
        {
            "id": "MONDO:0012637",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012637",
            "name": "CDG syndrome type IIg",
            "description": ""
        },
        {
            "id": "MONDO:0012637",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012637",
            "name": "CDG-IIg",
            "description": ""
        },
        {
            "id": "MONDO:0012637",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012637",
            "name": "CDG2G",
            "description": ""
        },
        {
            "id": "MONDO:0012637",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012637",
            "name": "COG1-CDG",
            "description": ""
        },
        {
            "id": "MONDO:0012637",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012637",
            "name": "COG1-congenital disorder of glycosylation",
            "description": ""
        },
        {
            "id": "MONDO:0012637",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012637",
            "name": "carbohydrate deficient glycoprotein syndrome type IIg",
            "description": ""
        },
        {
            "id": "MONDO:0012637",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012637",
            "name": "congenital disorder of glycosylation type 2g",
            "description": ""
        },
        {
            "id": "MONDO:0012637",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012637",
            "name": "congenital disorder of glycosylation type IIg",
            "description": ""
        },
        {
            "id": "MONDO:0012637",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012637",
            "name": "CDG 2G",
            "description": ""
        },
        {
            "id": "MONDO:0012637",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012637",
            "name": "COG1-CDG (CDG-IIg)",
            "description": ""
        },
        {
            "id": "MONDO:0012637",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012637",
            "name": "congenital disorder of glycosylation, type IIg",
            "description": ""
        },
        {
            "id": "MIM:611209",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/611209",
            "name": "Congenital disorder of glycosylation 2G",
            "description": "Congenital disorder of glycosylation 2G"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070259"
    ],
    "unlinked_id_list": []
}