{
    "disease_id": "DOID:0111776", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013120", 
            "name": "46,XY gonadal dysgenesis, complete, Cbx2-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013120", 
            "name": "SRXY5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013120", 
            "name": "46,XY SEX reversal 5; SRXY5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013120", 
            "name": "46,XY Sex reversal type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013120", 
            "name": "disorder of Sex development, 46,XY, Cbx2-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013120", 
            "name": "Sex reversal, XY, Cbx2-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013120", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013120", 
            "name": "46,XY Sex reversal, Cbx2-related"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111776", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111776", 
            "name": "SRXY5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111776", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111776", 
            "name": "46,XY gonadal dysgenesis, complete, CBX2-related"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111776", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111776", 
            "name": "46,XY sex reversal, CBX2-related"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111776", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111776", 
            "name": "disorder of sex development, 46,XY, CBX2-related"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111776", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111776", 
            "name": "sex reversal, XY, CBX2-related"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111776", 
        "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 homozygous or compound heterozygous mutation in CBX2 on chromosome 17q25.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111776", 
        "name": "46,XY sex reversal 5"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613080", 
            "id": "613080", 
            "database": "MIM"
        }
    ]
}