{
    "disease_id": "DOID:0070266", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014746", 
            "name": "SLC39A8-CDG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014746", 
            "name": "CDG2N"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014746", 
            "name": "CDG syndrome type IIn"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014746", 
            "name": "congenital disorder of glycosylation type 2n"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014746", 
            "name": "CDG-IIn"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014746", 
            "name": "carbohydrate deficient glycoprotein syndrome type IIn"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014746", 
            "name": "congenital disorder of glycosylation, type IIn"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014746", 
            "name": "SLC39A8 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014746", 
            "name": "congenital disorder of glycosylation, type IIn; CDG2N"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014746", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014746", 
            "name": "CDG IIn"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070266", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070266", 
            "name": "Carbohydrate deficient glycoprotein syndrome type IIn"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070266", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070266", 
            "name": "CDG IIn"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070266", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070266", 
            "name": "CDG syndrome type IIn"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070266", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070266", 
            "name": "CDG2N"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070266", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070266", 
            "name": "CDGIIdn"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070266", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070266", 
            "name": "Congenital disorder of glycosylation type 2n"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070266", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070266", 
            "name": "SLC39A8-CDG"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070266", 
        "description": "A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of SLC39A8 on chromosome 4q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070266", 
        "name": "congenital disorder of glycosylation type IIn"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070266#disease-associations", 
            "id": "0070266", 
            "database": "Alliance of Genome Resources"
        }
    ]
}