{
    "disease_id": "DOID:0070258", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011342", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011342", 
            "name": "SLC35A1-CDG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011342", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011342", 
            "name": "congenital disorder of glycosylation, type IIf"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011342", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011342", 
            "name": "CDG syndrome type IIf"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011342", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011342", 
            "name": "congenital disorder of glycosylation, type IIf; CDG2F"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011342", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011342", 
            "name": "congenital disorder of glycosylation type 2f"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011342", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011342", 
            "name": "CDG2F"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011342", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011342", 
            "name": "CDG-IIf"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011342", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011342", 
            "name": "carbohydrate deficient glycoprotein syndrome type IIf"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011342", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011342", 
            "name": "CDG IIf"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011342", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011342", 
            "name": "SLC35A1-CDG (CDG-IIf)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011342", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011342", 
            "name": "CMP-sialic acid transporter deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070258", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070258", 
            "name": "Carbohydrate deficient glycoprotein syndrome type IIf"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070258", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070258", 
            "name": "CDG IIf"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070258", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070258", 
            "name": "CDG2F"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070258", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070258", 
            "name": "CDGIIdf"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070258", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070258", 
            "name": "CMP-sialic acid transporter deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070258", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070258", 
            "name": "SLC35A1-CDG"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070258", 
        "description": "A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of SLC35A1 on chromosome 6q15.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070258", 
        "name": "congenital disorder of glycosylation type IIf"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070258#disease-associations", 
            "id": "0070258", 
            "database": "Alliance of Genome Resources"
        }
    ]
}