{
    "disease_id": "DOID:0080572", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014270", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014270", 
            "name": "STT3A-CDG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014270", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014270", 
            "name": "congenital disorder of glycosylation type 1w"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014270", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014270", 
            "name": "CDG-Iw"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014270", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014270", 
            "name": "CDG1W"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014270", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014270", 
            "name": "CDG Iw"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014270", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014270", 
            "name": "CDG syndrome type Iw"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014270", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014270", 
            "name": "congenital disorder of glycosylation type Iw"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014270", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014270", 
            "name": "congenital disorder of glycosylation, type Iw; CDG1W"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014270", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014270", 
            "name": "congenital disorder of glycosylation, type Iw"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080572", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080572", 
            "name": "congenital disorder of glycosylation 1w"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080572", 
        "description": "A congenital disorder of glycosylation I that is characterized by developmental delay, intellectual disability, failure to thrive, hypotonia and seizures and has_material_basis_in homozygous mutation in the STT3A gene on chromosome 11q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080572", 
        "name": "congenital disorder of glycosylation Iw"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080572#disease-associations", 
            "id": "0080572", 
            "database": "Alliance of Genome Resources"
        }
    ]
}