{
    "disease_id": "DOID:0111774", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009301", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009301", 
            "name": "46,XY Sex reversal, partial or complete, Dhh-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009301", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009301", 
            "name": "46,XY gonadal dysgenesis, partial or complete, Dhh-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009301", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009301", 
            "name": "SRXY7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009301", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009301", 
            "name": "46,XY SEX reversal 7; SRXY7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009301", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009301", 
            "name": "46,XY Sex reversal type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009301", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009301", 
            "name": "gonadal dysgenesis, XY, Male-limited"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111774", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111774", 
            "name": "46,XY gonadal dysgenesis, partial or complete, DHH-related"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111774", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111774", 
            "name": "GDXYM"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111774", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111774", 
            "name": "46,XY sex reversal, partial or complete, DHH-related"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111774", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111774", 
            "name": "SRXY7"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111774", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111774", 
            "name": "gonadal dysgenesis, XY, male limited"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111774", 
        "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 DHH on chromosome 12q13.12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111774", 
        "name": "46,XY sex reversal 7"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111774#disease-associations", 
            "id": "0111774", 
            "database": "Alliance of Genome Resources"
        }
    ]
}