{
    "disease_id": "DOID:0050546", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013400", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013400", 
            "name": "46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013400", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013400", 
            "name": "cholesterol side-chain Cleavage deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013400", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013400", 
            "name": "XY sex reversal-adrenal failure syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013400", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013400", 
            "name": "p450scc deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013400", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013400", 
            "name": "XY sex reversal-adrenal failure"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013400", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013400", 
            "name": "adrenal insufficiency, congenital, with 46,XY SEX reversal, partial or complete"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013400", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013400", 
            "name": "46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050546", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050546", 
            "name": "P450scc DEFICIENCY"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050546", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050546", 
            "name": "ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIAL OR COMPLETE"
        }, 
        {
            "url": "https://www.omim.org/entry/613743", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:613743", 
            "name": "Adrenal insufficiency, congenital, with 46,XY sex reversal"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050546", 
        "description": "An adrenal gland disease that is characterized by cortisol deficiency, hypoaldosteronism and excessive or insufficient sex hormones, has_material_basis_in the mutation in the gene for 21-hydroxylase, 11beta-hydroxylase, 3beta-hydroxysteroid, 17alpha-hydroxylase or 20,22-desmolase.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050546", 
        "name": "congenital adrenal insufficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613743", 
            "id": "613743", 
            "database": "MIM"
        }
    ]
}