{
    "disease_id": "DOID:0090030", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012675", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012675", 
            "name": "CBG deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012675", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012675", 
            "name": "transcortin deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012675", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012675", 
            "name": "corticosteroid-binding globulin, elevated"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090030", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090030", 
            "name": "CBG deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090030", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090030", 
            "name": "transcortin deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090030", 
        "description": "An adrenal gland disease characterized by decreased levels of serum corticosteroid-binding globulin and cortisol, and in some cases hypo- or hypertension, and muscle fatigue that has_material_basis_in heterozygous or homozygous mutation in the SERPINA6 gene on chromosome 14q32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090030", 
        "name": "corticosteroid-binding globulin deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090030#disease-associations", 
            "id": "0090030", 
            "database": "Alliance of Genome Resources"
        }
    ]
}