{
    "disease_id": "DOID:0112271",
    "recommended_name": {
        "id": "DOID:0112271",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112271",
        "name": "spermatogenic failure 49",
        "description": "A spermatogenic failure characterized by multiple morphologic abnormalities of the sperm flagella resulting in markedly reduced or no progressive motility that has_material_basis_in homozygous or compound heterozygous mutation in the CFAP58 gene on chromosome 10q25.1."
    },
    "synonyms": [
        {
            "id": "DOID:0112271",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112271",
            "name": "SPGF98",
            "description": ""
        },
        {
            "id": "MONDO:0030868",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030868",
            "name": "spermatogenic failure 49",
            "description": ""
        },
        {
            "id": "MONDO:0030868",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030868",
            "name": "SPGF49",
            "description": ""
        },
        {
            "id": "MONDO:0030868",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030868",
            "name": "spermatogenic failure 49",
            "description": ""
        },
        {
            "id": "MIM:619144",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619144",
            "name": "Spermatogenic failure 49",
            "description": "Spermatogenic failure 49"
        }
    ]
}