{
    "disease_id": "DOID:0070599",
    "recommended_name": {
        "id": "DOID:0070599",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070599",
        "name": "X-linked spermatogenic failure 8",
        "description": "A spermatogenic failure characterized by sperm with head and midpiece defects, deformed and detached acrosomes, and markedly reduced progressive motility that has_material_basis_in hemizygous mutation in the CYLC1 gene on chromosome Xq21.1."
    },
    "synonyms": [
        {
            "id": "DOID:0070599",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070599",
            "name": "SPGFX8",
            "description": ""
        },
        {
            "id": "MONDO:0970943",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0970943",
            "name": "spermatogenic failure, X-linked, 8",
            "description": ""
        },
        {
            "id": "MIM:301119",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/301119",
            "name": "Spermatogenic failure, X-linked, 8",
            "description": "Spermatogenic failure, X-linked, 8"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070599"
    ],
    "unlinked_id_list": []
}