{
    "disease_id": "DOID:0070259", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012637", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012637", 
            "name": "COG1-CDG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012637", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012637", 
            "name": "CDG IIg"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012637", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012637", 
            "name": "congenital disorder of glycosylation, type IIg"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012637", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012637", 
            "name": "congenital disorder of glycosylation, type IIg; CDG2G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012637", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012637", 
            "name": "CDG syndrome type IIg"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012637", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012637", 
            "name": "congenital disorder of glycosylation type 2g"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012637", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012637", 
            "name": "COG1-CDG (CDG-IIg)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012637", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012637", 
            "name": "CDG 2G"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012637", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012637", 
            "name": "CDG-IIg"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012637", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012637", 
            "name": "carbohydrate deficient glycoprotein syndrome type IIg"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012637", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012637", 
            "name": "Cdgii/Cog1 Cerebrocostomandibular-like syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012637", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012637", 
            "name": "CDG2G"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070259", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070259", 
            "name": "Carbohydrate deficient glycoprotein syndrome type IIg"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070259", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070259", 
            "name": "CDG IIg"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070259", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070259", 
            "name": "CDG2G"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070259", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070259", 
            "name": "CDGII/COG1 cerebrocostomandibular-like syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070259", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070259", 
            "name": "CDGIIg"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070259", 
        "description": "A congenital disorder of glycosylation type II that has_material_basis_in a mutation of COG1 on chromosome 17q25.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070259", 
        "name": "congenital disorder of glycosylation type IIg"
    }, 
    "evidence": [
        {
            "url": "https://glycosmos.org/glycogenes/show?source=kegg&gene_id=9382", 
            "id": "9382", 
            "database": "GlyCosmos"
        }
    ]
}