{
    "disease_id": "DOID:0070264", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013810", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013810", 
            "name": "COG6-CGD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013810", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013810", 
            "name": "CDG IIL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013810", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013810", 
            "name": "CDG syndrome type IIL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013810", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013810", 
            "name": "congenital disorder of glycosylation type 2l"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013810", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013810", 
            "name": "congenital disorder of glycosylation, type IIL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013810", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013810", 
            "name": "CDGIIl"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013810", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013810", 
            "name": "CDG2L"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013810", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013810", 
            "name": "CDG-IIL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013810", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013810", 
            "name": "COG6-CDG (CDG-IIL)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013810", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013810", 
            "name": "congenital disorder of glycosylation, type IIL; CDG2L"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070264", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070264", 
            "name": "CDG IIl"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070264", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070264", 
            "name": "CDG syndrome type IIL"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070264", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070264", 
            "name": "CDG2L"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070264", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070264", 
            "name": "CDGIIdl"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070264", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070264", 
            "name": "COG6-CGD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070264", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070264", 
            "name": "Congenital disorder of glycosylation type 2l"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070264", 
        "description": "A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of COG6 on chromosome 13q14.11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070264", 
        "name": "congenital disorder of glycosylation type IIl"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070264#disease-associations", 
            "id": "0070264", 
            "database": "Alliance of Genome Resources"
        }
    ]
}