{
    "disease_id": "DOID:0111771", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007938", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007938", 
            "name": "46,XY gonadal dysgenesis, partial or complete, with 9P24.3 deletion"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007938", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007938", 
            "name": "SRXY4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007938", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007938", 
            "name": "46,XY SEX reversal 4; SRXY4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007938", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007938", 
            "name": "46,XY Sex reversal type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007938", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007938", 
            "name": "chromosome 9P24.3 deletion syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111771", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111771", 
            "name": "SRXY4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111771", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111771", 
            "name": "chromosome 9p24.3 deletion syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111771", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111771", 
            "name": "46,XY gonadal dysgenesis, partial or complete, with 9p24.3 deletion"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111771", 
        "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 but with the absence of other features of the chromosome 9p deletion syndrome that has_material_basis_in heterozygous deletion of a region on chromosome 9p.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111771", 
        "name": "46,XY sex reversal 4"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/154230", 
            "id": "154230", 
            "database": "MIM"
        }
    ]
}