{
    "disease_id": "DOID:0070265", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010478", 
            "name": "SLC35A2-CDG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010478", 
            "name": "CDG2M"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010478", 
            "name": "epileptic encephalopathy, early infantile, 22; EIEE22"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010478", 
            "name": "congenital disorder of glycosylation, type IIm; CDG2M"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010478", 
            "name": "CDG syndrome type IIm"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010478", 
            "name": "congenital disorder of glycosylation type 2m"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010478", 
            "name": "congenital disorder of glycosylation, type IIm"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010478", 
            "name": "CDG IIm"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010478", 
            "name": "CDG-IIm"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010478", 
            "name": "epileptic encephalopathy, early infantile, 22"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010478", 
            "name": "EIEE22"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070265", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070265", 
            "name": "Congenital disorder of glycosylation type 2m"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070265", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070265", 
            "name": "SLC35A2-CDG"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070265", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070265", 
            "name": "epileptic encephalopathy, early infantile, 22"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070265", 
        "description": "A congenital disorder of glycosylation type II that is characterized by infantile onset seizures, hypsarrhythmia, hypotonia, and severe intellectual disability with lack of speech and that has_material_basis_in X-linked dominant inheritance of hemizygous or heterozygous mutation in the SLC35A2 gene on chromosome Xp11.23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070265", 
        "name": "congenital disorder of glycosylation type IIm"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070265#disease-associations", 
            "id": "0070265", 
            "database": "Alliance of Genome Resources"
        }
    ]
}