{
    "disease_id": "DOID:0112259",
    "recommended_name": {
        "id": "DOID:0112259",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112259",
        "name": "Leydig cell hypoplasia",
        "description": "A pseudohermaphroditism that has_material_basis_in homozygous or compound heterozygous mutation in the LHCGR gene on chromosome 2p16.3."
    },
    "synonyms": [
        {
            "id": "DOID:0112259",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112259",
            "name": "46,XY disorder of sex development due to LH resistance or LHB deficiency",
            "description": ""
        },
        {
            "id": "DOID:0112259",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112259",
            "name": "46,XY DSD due to LH resistance or LHB deficiency",
            "description": ""
        },
        {
            "id": "DOID:0112259",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112259",
            "name": "46,XY DSD due to luteinizing hormone resistance or luteinizing hormone beta subunit deficiency",
            "description": ""
        },
        {
            "id": "DOID:0112259",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112259",
            "name": "46,XY disorder of sex development due to luteinizing hormone resistance or luteinizing hormone beta subunit deficiency",
            "description": ""
        }
    ],
    "children": [
        {
            "id": "DOID:0112260",
            "label": "Leydig cell hypoplasia type I",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0112259",
        "DOID:0112260"
    ],
    "unlinked_id_list": []
}