{
    "disease_id": "DOID:0070180",
    "recommended_name": {
        "id": "DOID:0070180",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070180",
        "name": "spermatogenic failure 11",
        "description": "A spermatogenic failure that is characterized by autosomal dominant inheritance of oligozoospermia and in some cases teratozoospermia and/or moderate asthenozoospermia that has_material_basis_in mutation in the KLHL10 gene on chromosome 17q21."
    },
    "synonyms": [
        {
            "id": "DOID:0070180",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070180",
            "name": "SPGF11",
            "description": ""
        },
        {
            "id": "MONDO:0014037",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014037",
            "name": "spermatogenic failure 11",
            "description": "Any azoospermia in which the cause of the disease is a mutation in the KLHL10 gene."
        },
        {
            "id": "MONDO:0014037",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014037",
            "name": "KLHL10 azoospermia",
            "description": ""
        },
        {
            "id": "MONDO:0014037",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014037",
            "name": "azoospermia caused by mutation in KLHL10",
            "description": ""
        },
        {
            "id": "MONDO:0014037",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014037",
            "name": "spermatogenic failure 11",
            "description": ""
        },
        {
            "id": "MONDO:0014037",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014037",
            "name": "spermatogenic failure type 11",
            "description": ""
        },
        {
            "id": "MONDO:0014037",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014037",
            "name": "SPGF11",
            "description": ""
        },
        {
            "id": "MIM:615081",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615081",
            "name": "Spermatogenic failure 11",
            "description": "Spermatogenic failure 11"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070180"
    ],
    "unlinked_id_list": []
}