{
    "disease_id": "DOID:0111772", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013066", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013066", 
            "name": "SRXY3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013066", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013066", 
            "name": "disorder of Sex development, 46,XY, Nr5A1-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013066", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013066", 
            "name": "46,XY Sex reversal type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013066", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013066", 
            "name": "46,XY gonadal dysgenesis, partial or complete, with or without adrenal failure"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013066", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013066", 
            "name": "46,XY Sex reversal, partial or complete, Nr5A1-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013066", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013066", 
            "name": "Sex reversal, XY, with or without adrenal failure"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013066", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013066", 
            "name": "46,XY SEX reversal 3; SRXY3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111772", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111772", 
            "name": "SRXY3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111772", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111772", 
            "name": "disorder of sex development, 46,XY, NR5A1-related"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111772", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111772", 
            "name": "sex reversal, XY, with or without adrenal failure"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111772", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111772", 
            "name": "46,XY sex reversal, partial or complete, NR5A1-related"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111772", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111772", 
            "name": "46,XY gonadal dysgenesis, partial or complete, with or without adrenal failure"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111772", 
        "description": "A 46 XY sex reversal characterized by an XY karyotype, phenotypically female genitalia and failure to develop secondary sexual characteristics at puberty including menstruation that has_material_basis_in heterozygous mutation in NR5A1 on chromosome 9q33.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111772", 
        "name": "46,XY sex reversal 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111772#disease-associations", 
            "id": "0111772", 
            "database": "Alliance of Genome Resources"
        }
    ]
}