{
    "disease_id": "DOID:0070255",
    "recommended_name": {
        "id": "DOID:0070255",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070255",
        "name": "congenital disorder of glycosylation type IIc",
        "description": "A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of the SLC35C1 gene on chromosome 11p11.2."
    },
    "synonyms": [
        {
            "id": "DOID:0070255",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070255",
            "name": "CDG IIc",
            "description": ""
        },
        {
            "id": "DOID:0070255",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070255",
            "name": "CDG2C",
            "description": ""
        },
        {
            "id": "DOID:0070255",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070255",
            "name": "CDGIIc",
            "description": ""
        },
        {
            "id": "DOID:0070255",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070255",
            "name": "Rambam-Hasharon syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009953",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009953",
            "name": "leukocyte adhesion deficiency type II",
            "description": "Leukocyte adhesion deficiency type II (LAD-II) is a form of LAD characterized by recurrent bacterial infections, severe growth delay and severe intellectual deficit."
        },
        {
            "id": "MONDO:0009953",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009953",
            "name": "CDG IIc",
            "description": ""
        },
        {
            "id": "MONDO:0009953",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009953",
            "name": "CDG syndrome type IIc",
            "description": ""
        },
        {
            "id": "MONDO:0009953",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009953",
            "name": "CDG-IIc",
            "description": ""
        },
        {
            "id": "MONDO:0009953",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009953",
            "name": "CDG2C",
            "description": ""
        },
        {
            "id": "MONDO:0009953",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009953",
            "name": "CDGIIc",
            "description": ""
        },
        {
            "id": "MONDO:0009953",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009953",
            "name": "LAD-II",
            "description": ""
        },
        {
            "id": "MONDO:0009953",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009953",
            "name": "LAD2",
            "description": ""
        },
        {
            "id": "MONDO:0009953",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009953",
            "name": "RHS",
            "description": ""
        },
        {
            "id": "MONDO:0009953",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009953",
            "name": "Rambam-Hasharon syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009953",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009953",
            "name": "SLC35C1-CDG",
            "description": ""
        },
        {
            "id": "MONDO:0009953",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009953",
            "name": "lad-II",
            "description": ""
        },
        {
            "id": "MONDO:0009953",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009953",
            "name": "lad-type II",
            "description": ""
        },
        {
            "id": "MONDO:0009953",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009953",
            "name": "leukocyte adhesion deficiency type 2",
            "description": ""
        },
        {
            "id": "MONDO:0009953",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009953",
            "name": "leukocyte adhesion deficiency type II",
            "description": ""
        },
        {
            "id": "MONDO:0009953",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009953",
            "name": "leukocyte adhesion deficiency, type II",
            "description": ""
        },
        {
            "id": "MONDO:0009953",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009953",
            "name": "sialyl-Lewis X defect",
            "description": ""
        },
        {
            "id": "MONDO:0009953",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009953",
            "name": "CDG 2C",
            "description": ""
        },
        {
            "id": "MONDO:0009953",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009953",
            "name": "SLC35C1-CDG (CDG-IIc)",
            "description": ""
        },
        {
            "id": "MONDO:0009953",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009953",
            "name": "congenital disorder of glycosylation type IIC",
            "description": ""
        },
        {
            "id": "MONDO:0009953",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009953",
            "name": "congenital disorder of glycosylation, type IIc",
            "description": ""
        },
        {
            "id": "MONDO:0009953",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009953",
            "name": "leukocyte adhesion deficiency, type 2",
            "description": ""
        },
        {
            "id": "MIM:266265",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/266265",
            "name": "Congenital disorder of glycosylation 2C",
            "description": "Congenital disorder of glycosylation 2C"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070255"
    ],
    "unlinked_id_list": []
}