{
    "disease_id": "DOID:0080556", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010998", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010998", 
            "name": "ALG3-CDG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010998", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010998", 
            "name": "CDG1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010998", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010998", 
            "name": "CDG 1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010998", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010998", 
            "name": "CDGS4 (formerly)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010998", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010998", 
            "name": "carbohydrate-deficient glycoprotein syndrome type IV (formerly)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010998", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010998", 
            "name": "CDG Id"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010998", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010998", 
            "name": "CDG syndrome type Id"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010998", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010998", 
            "name": "Cdgs, type IV, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010998", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010998", 
            "name": "congenital disorder of glycosylation type Id"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010998", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010998", 
            "name": "Cdgs, type IV"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010998", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010998", 
            "name": "CDGId"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010998", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010998", 
            "name": "congenital disorder of glycosylation, type Id; CDG1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010998", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010998", 
            "name": "mannosyltransferase 6 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010998", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010998", 
            "name": "congenital disorder of glycosylation, type Id"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010998", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010998", 
            "name": "carbohydrate-deficient glycoprotein syndrome, type IV, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010998", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010998", 
            "name": "congenital disorder of glycosylation type 1d"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010998", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010998", 
            "name": "carbohydrate deficient glycoprotein syndrome type Id"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010998", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010998", 
            "name": "carbohydrate-deficient glycoprotein syndrome, type IV"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010998", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010998", 
            "name": "CDG-Id"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010998", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010998", 
            "name": "ALG3-CDG (CDG-Id)"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080556", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080556", 
            "name": "congenital disorder of glycosylation 1d"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080556", 
        "description": "A congenital disorder of glycosylation I that is characterized by severe neurologic involvement associated with dysmorphism and visual impairment and has_material_basis_in homozygous or compound heterozygous mutation in the ALG3 gene on chromosome 3q27.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080556", 
        "name": "congenital disorder of glycosylation Id"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080556#disease-associations", 
            "id": "0080556", 
            "database": "Alliance of Genome Resources"
        }
    ]
}