{
    "disease_id": "DOID:0080156", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010264", 
            "name": "adrenal insufficiency, progressive, and hypogonadotropic hypogonadism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010264", 
            "name": "AHC with HHG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010264", 
            "name": "AHC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010264", 
            "name": "adrenal hypoplasia, congenital, with hypogonadotropic hypogonadism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010264", 
            "name": "cytomegalic adrenocortical hypoplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010264", 
            "name": "cytomegalic congenital adrenal hypoplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010264", 
            "name": "X-linked congenital adrenal hypoplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010264", 
            "name": "AHC with isolated gonadotropin deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010264", 
            "name": "adrenal hypoplasia, congenital; AHC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010264", 
            "name": "X-linked AHC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010264", 
            "name": "mineralocorticoid deficiency, isolated"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010264", 
            "name": "Addison disease, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010264", 
            "name": "adrenal hypoplasia congenita"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010264", 
            "name": "congenital adrenal hypoplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010264", 
            "name": "adrenal hypoplasia, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010264", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010264", 
            "name": "adrenal hypoplasia, congenital, with precocious puberty"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080156", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080156", 
            "name": "congenital adrenal hypoplasia"
        }, 
        {
            "url": "https://www.omim.org/entry/300200", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:300200", 
            "name": "Adrenal hypoplasia, congenital"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080156", 
        "description": "An adrenal cortical hypofunction that is characterized by a reduction in adrenal gland function resulting from incomplete development of the adrenal cortex and has_material_basis_in the nuclear receptor NR0B1 (DAX1) gene.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080156", 
        "name": "X-linked adrenal hypoplasia congenita"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/300200", 
            "id": "300200", 
            "database": "MIM"
        }
    ]
}