{
    "disease_id": "DOID:0080572",
    "recommended_name": {
        "id": "DOID:0080572",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080572",
        "name": "congenital disorder of glycosylation Iw",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0080572",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080572",
            "name": "congenital disorder of glycosylation 1w",
            "description": ""
        },
        {
            "id": "MONDO:0014270",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014270",
            "name": "STT3A-congenital disorder of glycosylation",
            "description": "STT3A-CDG is a form of congenital disorders of N-linked glycosylation characterized by developmental delay, intellectual disability, failure to thrive, hypotonia and seizures. STT3A-CDG is caused by mutations in the gene STT3A (11q23.3)."
        },
        {
            "id": "MONDO:0014270",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014270",
            "name": "CDG syndrome type Iw",
            "description": ""
        },
        {
            "id": "MONDO:0014270",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014270",
            "name": "CDG-Iw",
            "description": ""
        },
        {
            "id": "MONDO:0014270",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014270",
            "name": "CDG1W",
            "description": ""
        },
        {
            "id": "MONDO:0014270",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014270",
            "name": "STT3A-CDG",
            "description": ""
        },
        {
            "id": "MONDO:0014270",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014270",
            "name": "STT3A-congenital disorder of glycosylation",
            "description": ""
        },
        {
            "id": "MONDO:0014270",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014270",
            "name": "congenital disorder of glycosylation type 1w",
            "description": ""
        },
        {
            "id": "MONDO:0014270",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014270",
            "name": "congenital disorder of glycosylation type Iw",
            "description": ""
        },
        {
            "id": "MONDO:0014270",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014270",
            "name": "congenital disorder of glycosylation, type Iw, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0014270",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014270",
            "name": "congenital disorder of glycosylation, type Iw",
            "description": ""
        },
        {
            "id": "MIM:615596",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615596",
            "name": "Congenital disorder of glycosylation 1W, autosomal recessive",
            "description": "Congenital disorder of glycosylation 1W, autosomal recessive"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080572"
    ],
    "unlinked_id_list": []
}