{
    "disease_id": "DOID:0080564", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012117", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012117", 
            "name": "ALG9-CDG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012117", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012117", 
            "name": "congenital disorder of glycosylation type IL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012117", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012117", 
            "name": "congenital disorder of glycosylation type 1L"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012117", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012117", 
            "name": "CDG-IL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012117", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012117", 
            "name": "ALG9-CDG (CDG-IL)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012117", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012117", 
            "name": "mannosyltransferase 7-9 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012117", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012117", 
            "name": "CDG1L"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012117", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012117", 
            "name": "congenital disorder of glycosylation, type IL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012117", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012117", 
            "name": "CDG syndrome type IL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012117", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012117", 
            "name": "carbohydrate deficient glycoprotein syndrome type IL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012117", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012117", 
            "name": "carbohydrate deficient glycoprotein syndrome type 1L"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012117", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012117", 
            "name": "congenital disorder of glycosylation, type IL; CDG1L"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012117", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012117", 
            "name": "CDG 1L"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012117", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012117", 
            "name": "CDG IL"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080564", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080564", 
            "name": "congenital disorder of glycosylation 1l"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080564", 
        "description": "A congenital disorder of glycosylation I that is characterized by progressive microcephaly, hypotonia, developmental delay, drug-resistant infantile epilepsy, and hepatomegaly and has_material_basis_in homozygous mutation in the ALG9 gene on chromosome 11q23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080564", 
        "name": "congenital disorder of glycosylation Il"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080564#disease-associations", 
            "id": "0080564", 
            "database": "Alliance of Genome Resources"
        }
    ]
}