{
    "disease_id": "DOID:0070269", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054559", 
            "name": "congenital disorder of glycosylation, type IIq"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054559", 
            "name": "CDG2Q"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054559", 
            "name": "congenital disorder of glycosylation, type IIq; CDG2Q"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054559", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054559", 
            "name": "CDG Iiq"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070269", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070269", 
            "name": "CDG IIq"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070269", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070269", 
            "name": "CDG2Q"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070269", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070269", 
            "name": "CDGIIdq"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070269", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070269", 
            "name": "COG2-CDG"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070269", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070269", 
            "name": "COG2-related congenital disorder of glycosylation"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070269", 
        "description": "A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of COG2 on chromosome 1q42.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070269", 
        "name": "congenital disorder of glycosylation type IIq"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070269#disease-associations", 
            "id": "0070269", 
            "database": "Alliance of Genome Resources"
        }
    ]
}