{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011933", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011933", 
            "name": "ALG2-CDG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011933", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011933", 
            "name": "ALG2-CDG (CDG-II)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011933", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011933", 
            "name": "congenital disorder of glycosylation, type II; CDG1I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011933", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011933", 
            "name": "CDG syndrome type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011933", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011933", 
            "name": "congenital disorder of glycosylation type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011933", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011933", 
            "name": "CDG II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011933", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011933", 
            "name": "CDG1I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011933", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011933", 
            "name": "carbohydrate-deficient glycoprotein syndrome type 1I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011933", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011933", 
            "name": "CDG 1I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011933", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011933", 
            "name": "mannosyltransferase 2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011933", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011933", 
            "name": "congenital disorder of glycosylation type 1i"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011933", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011933", 
            "name": "carbohydrate deficient glycoprotein syndrome type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011933", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011933", 
            "name": "CDG-II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011933", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011933", 
            "name": "congenital disorder of glycosylation, type II"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080561", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080561", 
            "name": "congenital disorder of glycosylation 1i"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080561", 
        "description": "A congenital disorder of glycosylation I that is characterized by iris coloboma, cataract, infantile spasms, developmental delay and abnormal coagulation factors and has_material_basis_in compound heterozygous mutation in the ALG2 gene on chromosome 9q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080561", 
        "name": "congenital disorder of glycosylation Ii"
    }, 
    "evidence": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011933", 
            "id": "0011933", 
            "database": "MONDO"
        }, 
        {
            "url": "https://www.omim.org/entry/607906", 
            "id": "607906", 
            "database": "MIM"
        }
    ]
}