{
    "disease_id": "DOID:0112335",
    "recommended_name": {
        "id": "DOID:0112335",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112335",
        "name": "spermatogenic failure 54",
        "description": "A spermatogenic failure characterized by male infertility due to oligoteratoasthenozoospermia, with markedly reduced sperm counts and severely reduced or absent sperm motility that has_material_basis_in homozygous or compound heterozygous mutation in the CATIP gene on chromosome 2q35."
    },
    "synonyms": [
        {
            "id": "DOID:0112335",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112335",
            "name": "SPGF54",
            "description": ""
        },
        {
            "id": "MONDO:0023664",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0023664",
            "name": "spermatogenic failure 54",
            "description": ""
        },
        {
            "id": "MONDO:0023664",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0023664",
            "name": "SPGF54",
            "description": ""
        },
        {
            "id": "MIM:619379",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619379",
            "name": "Spermatogenic failure 54",
            "description": "Spermatogenic failure 54"
        }
    ]
}
