{
    "disease_id": "DOID:0111922",
    "recommended_name": {
        "id": "DOID:0111922",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111922",
        "name": "spermatogenic failure 31",
        "description": "A spermatogenic failure characterized by oligozoospermia with a high proportion of acephalic sperm that has_material_basis_in homozygous or compound heterozygous mutation in PMFBP1 on chromosome 16q22.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111922",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111922",
            "name": "SPGF31",
            "description": ""
        },
        {
            "id": "MONDO:0020852",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020852",
            "name": "spermatogenic failure 31",
            "description": ""
        },
        {
            "id": "MONDO:0020852",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020852",
            "name": "SPGF31",
            "description": ""
        },
        {
            "id": "MONDO:0020852",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020852",
            "name": "spermatogenic failure 31; SPGF31",
            "description": ""
        },
        {
            "id": "MIM:618112",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618112",
            "name": "Spermatogenic failure 31",
            "description": "Spermatogenic failure 31"
        }
    ]
}