{
    "disease_id": "DOID:0112260",
    "recommended_name": {
        "id": "DOID:0112260",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112260",
        "name": "Leydig cell hypoplasia type I",
        "description": "A Leydig cell hypoplasia characterized by 46,XY male pseudohermaphroditism, low testosterone and high LH levels, total lack of responsiveness to LH/CG challenge, lack of breast development, and absent development of secondary male sex characteristics that has_material_basis_in homozygous or compound heterozygous complete inactivation mutation in the LHCGR gene on chromosome 2p16.3."
    },
    "synonyms": [
        {
            "id": "DOID:0112260",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112260",
            "name": "46,XY DSD due to complete luteinizing hormone receptor inactivation",
            "description": ""
        },
        {
            "id": "DOID:0112260",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112260",
            "name": "46,XY disorder of sex development due to complete LH resistance",
            "description": ""
        },
        {
            "id": "DOID:0112260",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112260",
            "name": "46,XY disorder of sex development due to complete luteinizing hormone resistance",
            "description": ""
        },
        {
            "id": "DOID:0112260",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112260",
            "name": "46,XY DSD due to complete LH receptor inactivation",
            "description": ""
        },
        {
            "id": "DOID:0112260",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112260",
            "name": "46,XY DSD due to complete LH resistance",
            "description": ""
        },
        {
            "id": "DOID:0112260",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112260",
            "name": "46,XY DSD due to complete luteinizing hormone resistance",
            "description": ""
        },
        {
            "id": "DOID:0112260",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112260",
            "name": "46,XY disorder of sex development due to complete luteinizing hormone receptor inactivation",
            "description": ""
        },
        {
            "id": "DOID:0112260",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112260",
            "name": "Leydig cell hypoplasia due to complete luteinizing hormone resistance",
            "description": ""
        },
        {
            "id": "DOID:0112260",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112260",
            "name": "Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation",
            "description": ""
        },
        {
            "id": "DOID:0112260",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112260",
            "name": "Leydig cell hypoplasia due to complete LH receptor inactivation",
            "description": ""
        },
        {
            "id": "DOID:0112260",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112260",
            "name": "46,XY disorder of sex development due to complete LH receptor inactivation",
            "description": ""
        },
        {
            "id": "MONDO:0009384",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009384",
            "name": "Leydig cell hypoplasia, type 1",
            "description": "Any Leydig cell hypoplasia in which the cause of the disease is a mutation in the LHCGR gene."
        },
        {
            "id": "MONDO:0009384",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009384",
            "name": "LHCGR Leydig cell hypoplasia",
            "description": ""
        },
        {
            "id": "MONDO:0009384",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009384",
            "name": "Leydig cell hypoplasia caused by mutation in LHCGR",
            "description": ""
        },
        {
            "id": "MONDO:0009384",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009384",
            "name": "leydig cell hypoplasia with hypergonadotropic hypogonadism",
            "description": ""
        },
        {
            "id": "MONDO:0009384",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009384",
            "name": "leydig cell hypoplasia with pseudohermaphroditism",
            "description": ""
        },
        {
            "id": "MONDO:0009384",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009384",
            "name": "Leydig cell Hypoplasia, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0009384",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009384",
            "name": "Leydig cell agenesis",
            "description": ""
        },
        {
            "id": "MONDO:0009384",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009384",
            "name": "Leydig cell hypoplasia with male pseudohermaphroditism",
            "description": ""
        },
        {
            "id": "MONDO:0009384",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009384",
            "name": "Leydig cell hypoplasia, complete",
            "description": ""
        },
        {
            "id": "MONDO:0009384",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009384",
            "name": "Leydig cell hypoplasia, partial",
            "description": ""
        },
        {
            "id": "MONDO:0009384",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009384",
            "name": "Leydig cell hypoplasia, type I",
            "description": ""
        },
        {
            "id": "MONDO:0009384",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009384",
            "name": "hypergonadotropic hypogonadism, Male, due to Lhcgr defect",
            "description": ""
        },
        {
            "id": "MONDO:0009384",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009384",
            "name": "luteinizing hormone resistance, female",
            "description": ""
        },
        {
            "id": "MIM:238320",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/238320",
            "name": "Luteinizing hormone resistance",
            "description": "Luteinizing hormone resistance"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112260"
    ],
    "unlinked_id_list": []
}