{
    "disease_id": "DOID:0070256",
    "recommended_name": {
        "id": "DOID:0070256",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070256",
        "name": "congenital disorder of glycosylation type IId",
        "description": "A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of the B4GALT1 gene on chromosome 9p21.1."
    },
    "synonyms": [
        {
            "id": "DOID:0070256",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070256",
            "name": "CDG IId",
            "description": ""
        },
        {
            "id": "DOID:0070256",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070256",
            "name": "CDG2D",
            "description": ""
        },
        {
            "id": "DOID:0070256",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070256",
            "name": "CDGIId",
            "description": ""
        },
        {
            "id": "MONDO:0011772",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011772",
            "name": "B4GALT1-congenital disorder of glycosylation",
            "description": "B4GALT1-CDG is a congenital disorder of glycosylation characterized by macrocephaly due to Dandy-Walker malformation, hydrocephaly, hypotonia, myopathy and coagulation anomalies. To date, only one case has been reported. The syndrome is associated with mutations in the GALT1 gene (localized to region q13 of chromosome 9) leading to a deficiency in the Golgi apparatus enzyme beta-1,4-galactosyl transferase."
        },
        {
            "id": "MONDO:0011772",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011772",
            "name": "B4GALT1-CDG",
            "description": ""
        },
        {
            "id": "MONDO:0011772",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011772",
            "name": "B4GALT1-congenital disorder of glycosylation",
            "description": ""
        },
        {
            "id": "MONDO:0011772",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011772",
            "name": "Beta-1,4-galactosyltransferase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011772",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011772",
            "name": "CDG syndrome type IId",
            "description": ""
        },
        {
            "id": "MONDO:0011772",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011772",
            "name": "CDG-IId",
            "description": ""
        },
        {
            "id": "MONDO:0011772",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011772",
            "name": "CDG2D",
            "description": ""
        },
        {
            "id": "MONDO:0011772",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011772",
            "name": "carbohydrate deficient glycoprotein syndrome type IId",
            "description": ""
        },
        {
            "id": "MONDO:0011772",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011772",
            "name": "congenital disorder of glycosylation type 2d",
            "description": ""
        },
        {
            "id": "MONDO:0011772",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011772",
            "name": "congenital disorder of glycosylation type IId",
            "description": ""
        },
        {
            "id": "MONDO:0011772",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011772",
            "name": "B4GALT1-CDG (CDG-IId)",
            "description": ""
        },
        {
            "id": "MONDO:0011772",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011772",
            "name": "CDG 2D",
            "description": ""
        },
        {
            "id": "MONDO:0011772",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011772",
            "name": "congenital disorder of glycosylation, type IId",
            "description": ""
        },
        {
            "id": "MIM:607091",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607091",
            "name": "Congenital disorder of glycosylation 2D",
            "description": "Congenital disorder of glycosylation 2D"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070256"
    ],
    "unlinked_id_list": []
}