{
    "disease_id": "DOID:0050811", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008727", 
            "name": "congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008727", 
            "name": "type II 3-beta-hydroxysteroid dehydrogenase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008727", 
            "name": "3-BETA-hydroxysteroid dehydrogenase, type II, deficiency OF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008727", 
            "name": "CAH due to 3-beta-hydroxysteroid dehydrogenase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008727", 
            "name": "adrenal hyperplasia 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008727", 
            "name": "HSD3B deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008727", 
            "name": "3b-hydroxysteroid dehydrogenase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008727", 
            "name": "3-Beta-HSD deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008727", 
            "name": "adrenal hyperplasia II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008727", 
            "name": "adrenal hyperplasia, congenital, due to 3-BETA-hydroxysteroid dehydrogenase 2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008727", 
            "name": "3-beta HSD deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008727", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008727", 
            "name": "3-Beta-hydroxysteroid dehydrogenase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050811", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050811", 
            "name": "adrenal hyperplasia 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050811", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050811", 
            "name": "congenital lipoid adrenal hyperplasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050811", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050811", 
            "name": "lipoid CAH"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050811", 
        "description": "A steroid inherited metabolic disorder that is characterized by adrenal insufficiency and variable degrees of hyper or hypo androgeny manifestations resulting from steroidogenic enzyme deficiency.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050811", 
        "name": "congenital adrenal hyperplasia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050811#disease-associations", 
            "id": "0050811", 
            "database": "Alliance of Genome Resources"
        }
    ]
}