{
    "disease_id": "DOID:0070255", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009953", 
            "name": "leukocyte adhesion deficiency type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009953", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009953", 
            "name": "SLC35C1-CDG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009953", 
            "name": "leukocyte adhesion deficiency, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009953", 
            "name": "CDG syndrome type IIc"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009953", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009953", 
            "name": "LAD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009953", 
            "name": "congenital disorder of glycosylation, type IIc; CDG2C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009953", 
            "name": "Rambam-Hasharon syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009953", 
            "name": "lad-II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009953", 
            "name": "congenital disorder of glycosylation, type IIc"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009953", 
            "name": "CDGIIc"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009953", 
            "name": "CDG-IIc"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009953", 
            "name": "RHS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009953", 
            "name": "sialyl-Lewis X defect"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009953", 
            "name": "lad-type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009953", 
            "name": "CDG2C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009953", 
            "name": "CDG IIc"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009953", 
            "name": "leukocyte adhesion deficiency, type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009953", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009953", 
            "name": "CDG 2C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070255", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070255", 
            "name": "CDG IIc"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070255", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070255", 
            "name": "CDG2C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070255", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070255", 
            "name": "CDGIIc"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070255", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070255", 
            "name": "Rambam-Hasharon syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070255", 
        "description": "A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of SLC35C1 on chromosome 11p11.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070255", 
        "name": "congenital disorder of glycosylation type IIc"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070255#disease-associations", 
            "id": "0070255", 
            "database": "Alliance of Genome Resources"
        }
    ]
}