{
    "disease_id": "DOID:0080554", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0080554", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080554", 
            "name": "congenital disorder of glycosylation 1b"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "(15q24.1).", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "MPI-CDG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "SLSJ syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "congenital disorder of glycosylation, type IB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "CDG 1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "congenital disorder of glycosylation type IB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "congenital disorder of glycosylation, type IB; CDG1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "MPI-CDG (CDG-Ib)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "carbohydrate-deficient glycoprotein syndrome type 1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "Mpi deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "CDG1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "phosphomannose isomerase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "Mannosephosphate isomerase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "carbohydrate deficient glycoprotein syndrome type IB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "Saguenay Lac Saint Jean syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "CDG syndrome type IB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "CDG gastrointestinal type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "Protein-losing enteropathy-hepatic fibrosis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "CDG, gastrointestinal type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "congenital disorder of glycosylation type 1b"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "Slsj syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "Saguenay-Lac Saint-Jean syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "CDG-Ib"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011257", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011257", 
            "name": "CDG Ib"
        }, 
        {
            "url": "https://www.omim.org/entry/602579", 
            "description": "Congenital disorder of glycosylation 1B", 
            "resource": "MIM", 
            "id": "MIM:602579", 
            "name": "Congenital disorder of glycosylation 1B"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080554", 
        "description": "A congenital disorder of glycosylation I that is characterized by protein-losing enteropathy, cyclic vomiting, profound hypoglycemia, failure to thrive, liver fibrosis, protein-losing enteropathy with hypoalbuminaemia, life-threatening intestinal bleeding of diffuse origin, protein C and S deficiency, low anti-thrombine III levels and has_material_basis_in compound heterozygous mutation in the gene encoding mannosephosphate isomerase on chromosome 15q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080554", 
        "name": "congenital disorder of glycosylation Ib"
    }
}