{
    "disease_id": "DOID:0111773", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013664", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013664", 
            "name": "46,XY disorder of sex development due to testicular 17,20-desmolase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013664", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013664", 
            "name": "SRXY8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013664", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013664", 
            "name": "male pseudohermaphroditism due to deficiency of testicular 17,20-desmolase"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013664", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013664", 
            "name": "46,XY sex reversal 8; SRXY8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013664", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013664", 
            "name": "46,XY sex reversal type 8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111773", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111773", 
            "name": "SRXY8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111773", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111773", 
            "name": "TDD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111773", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111773", 
            "name": "male pseudohermaphroditism due to deficiency of testicular 17,20-desmolase"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111773", 
        "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 AKR1C2 on chromosome 10p15.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111773", 
        "name": "46,XY sex reversal 8"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111773#disease-associations", 
            "id": "0111773", 
            "database": "Alliance of Genome Resources"
        }
    ]
}