{
    "disease_id": "DOID:0112352",
    "recommended_name": {
        "id": "DOID:0112352",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112352",
        "name": "spermatogenic failure 58",
        "description": "A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella and immotile or severely reduced progressive motility of sperm that has_material_basis_in homozygous or compound heterozygous mutation in the IFT74 gene on chromosome 9p21.2."
    },
    "synonyms": [
        {
            "id": "DOID:0112352",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112352",
            "name": "SPGF58",
            "description": ""
        },
        {
            "id": "MONDO:0030463",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030463",
            "name": "spermatogenic failure 58",
            "description": ""
        },
        {
            "id": "MONDO:0030463",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030463",
            "name": "SPGF58",
            "description": ""
        },
        {
            "id": "MIM:619585",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619585",
            "name": "Spermatogenic failure 58",
            "description": "Spermatogenic failure 58"
        }
    ]
}