{
    "disease_id": "DOID:4367", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009025", 
            "name": "apparent mineralocorticoid excess"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009025", 
            "name": "cortisol 11-Beta-ketoreductase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009025", 
            "name": "Ulick syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009025", 
            "name": "Ame1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009025", 
            "name": "apparent mineralocorticoid EXCESS; AME"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009025", 
            "name": "11 Beta-hydroxysteroid dehydrogenase type 2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009025", 
            "name": "AME"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009025", 
            "name": "ape"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009025", 
            "name": "11-beta-hydroxysteroid dehydrogenase deficiency type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009025", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009025", 
            "name": "AME 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:4367", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:4367", 
            "name": "Ulick syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:4367", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:4367", 
            "name": "11-beta-hydroxysteroid dehydrogenase deficiency type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:4367", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:4367", 
            "name": "cortisol 11-beta-ketoreductase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:4367", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:4367", 
            "name": "syndrome of apparent mineralocorticoid excess"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:4367", 
        "description": "A steroid inherited metabolic disorder characterized by decreased conversion of biologically active cortisol to inactive cortisone resulting in low aldosterone levels, metabolic alkalosis, hypernatremia, hypokalemia and early-onset severe hypertension that has_material_basis_in homozygous or compound heterozygous mutation in the HSD11B2 gene on chromosome 16.", 
        "resource": "Disease Ontology", 
        "id": "DOID:4367", 
        "name": "apparent mineralocorticoid excess syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/4367#disease-associations", 
            "id": "4367", 
            "database": "Alliance of Genome Resources"
        }
    ]
}