{
    "disease_id": "DOID:0111912",
    "recommended_name": {
        "id": "DOID:0111912",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111912",
        "name": "spermatogenic failure 41",
        "description": "A spermatogenic failure characterized by oligozoospermia and multiple morphologic abnormalities of the flagella that has_material_basis_in homozygous or compound heterozygous mutation in the CFAP70 gene on chromosome 10q22.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111912",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111912",
            "name": "SPGF41",
            "description": ""
        },
        {
            "id": "MONDO:0032863",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032863",
            "name": "spermatogenic failure 41",
            "description": ""
        },
        {
            "id": "MONDO:0032863",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032863",
            "name": "SPGF41",
            "description": ""
        },
        {
            "id": "MIM:618670",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618670",
            "name": "Spermatogenic failure 41",
            "description": "Spermatogenic failure 41"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111912"
    ],
    "unlinked_id_list": []
}