{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014271", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014271", 
            "name": "STT3B-CDG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014271", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014271", 
            "name": "congenital disorder of glycosylation type 1x"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014271", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014271", 
            "name": "CDG IX"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014271", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014271", 
            "name": "CDG-Ix"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014271", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014271", 
            "name": "carbohydrate deficient glycoprotein syndrome type IX"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014271", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014271", 
            "name": "CDG1X"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014271", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014271", 
            "name": "CDG syndrome type IX"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014271", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014271", 
            "name": "congenital disorder of glycosylation type IX"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014271", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014271", 
            "name": "congenital disorder of glycosylation, type IX; CDG1X"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014271", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014271", 
            "name": "congenital disorder of glycosylation, type IX"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080573", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080573", 
            "name": "congenital disorder of glycosylation 1x"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080573", 
        "description": "A congenital disorder of glycosylation I that is characterized by intrauterine growth retardation, microcephaly, failure to thrive, developmental delay, intellectual disability, hypotonia, seizures, optic nerve atrophy and respiratory difficulties and has_material_basis_in homozygous mutation in the STT3B gene on chromosome 3p23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080573", 
        "name": "congenital disorder of glycosylation Ix"
    }, 
    "evidence": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014271", 
            "id": "0014271", 
            "database": "MONDO"
        }, 
        {
            "url": "https://www.omim.org/entry/615597", 
            "id": "615597", 
            "database": "MIM"
        }
    ]
}