{
    "disease_id": "DOID:0070259",
    "recommended_name": {
        "id": "DOID:0070259",
        "resource": "Disease Ontology",
        "url": "http://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 COG1 on chromosome 17q25.1."
    },
    "synonyms": [
        {
            "id": "DOID:0070259",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070259",
            "name": "Carbohydrate deficient glycoprotein syndrome type IIg",
            "description": ""
        },
        {
            "id": "DOID:0070259",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070259",
            "name": "CDG IIg",
            "description": ""
        },
        {
            "id": "DOID:0070259",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070259",
            "name": "CDG2G",
            "description": ""
        },
        {
            "id": "DOID:0070259",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070259",
            "name": "CDGII/COG1 cerebrocostomandibular-like syndrome",
            "description": ""
        },
        {
            "id": "DOID:0070259",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070259",
            "name": "CDGIIg",
            "description": ""
        },
        {
            "id": "DOID:0070259",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070259",
            "name": "Congenital disorder of glycosylation type IIg",
            "description": ""
        },
        {
            "id": "MONDO:0012637",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012637",
            "name": "COG1-CDG",
            "description": "COG1-CDG is an extremely rare form of CDG syndrome (see this term) 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 IIg",
            "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": "congenital disorder of glycosylation type IIg",
            "description": ""
        },
        {
            "id": "MONDO:0012637",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012637",
            "name": "congenital disorder of glycosylation, type IIg; CDG2G",
            "description": ""
        },
        {
            "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": "congenital disorder of glycosylation type 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": "CDG 2G",
            "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": "carbohydrate deficient glycoprotein syndrome type IIg",
            "description": ""
        },
        {
            "id": "MONDO:0012637",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012637",
            "name": "Cdgii/Cog1 Cerebrocostomandibular-like syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012637",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012637",
            "name": "CDG2G",
            "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"
        }
    ]
}