{
    "disease_id": "DOID:0070260", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012635", 
            "name": "COG8-CDG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012635", 
            "name": "congenital disorder of glycosylation type 2h"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012635", 
            "name": "congenital disorder of glycosylation, type IIh"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012635", 
            "name": "carbohydrate deficient glycoprotein syndrome type IIh"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012635", 
            "name": "CDG-IIh"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012635", 
            "name": "congenital disorder of glycosylation, type IIh; CDG2H"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012635", 
            "name": "CDG2H"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012635", 
            "name": "CDG syndrome type IIh"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012635", 
            "name": "CDG IIh"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012635", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012635", 
            "name": "COG8-CDG (CDG-IIh)"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070260", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070260", 
            "name": "CDG IIh"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070260", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070260", 
            "name": "CDG2H"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070260", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070260", 
            "name": "CDGIIdh"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070260", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070260", 
            "name": "COG8-CDG"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070260", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070260", 
            "name": "Congenital disorder of glycosylation type 2h"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070260", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070260", 
            "name": "Carbohydrate deficient glycoprotein syndrome type IIh"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070260", 
        "description": "A congenital disorder of glycosylation type II that has_material_basis_in a mutation of COG8 on chromosome 16q22.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070260", 
        "name": "congenital disorder of glycosylation type IIh"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070260#disease-associations", 
            "id": "0070260", 
            "database": "Alliance of Genome Resources"
        }
    ]
}