{
    "disease_id": "DOID:0111927",
    "recommended_name": {
        "id": "DOID:0111927",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111927",
        "name": "spermatogenic failure 37",
        "description": "A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella, asthenoteratozoospermia, and infertility that has_material_basis_in homozygous or compound heterozygous mutation in TTC21A on chromosome 3p22.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111927",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111927",
            "name": "SPGF37",
            "description": ""
        },
        {
            "id": "MIM:618429",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618429",
            "name": "Spermatogenic failure 37",
            "description": "Spermatogenic failure 37"
        }
    ]
}