{
    "disease_id": "DOID:0112109",
    "recommended_name": {
        "id": "DOID:0112109",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0112109",
        "name": "spermatogenic failure 44",
        "description": "A spermatogenic failure characterized by high prevalence of acephalic sperm and reduced progressive motility of sperm that has_material_basis_in homozygous or compound heterozygous mutation in the CEP112 gene on chromosome 17q24.1."
    },
    "synonyms": [
        {
            "id": "DOID:0112109",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112109",
            "name": "SPGF44",
            "description": ""
        },
        {
            "id": "MONDO:0033622",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033622",
            "name": "spermatogenic failure 44",
            "description": ""
        },
        {
            "id": "MONDO:0033622",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033622",
            "name": "SPGF44",
            "description": ""
        },
        {
            "id": "MIM:619044",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619044",
            "name": "Spermatogenic failure 44",
            "description": "Spermatogenic failure 44"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112109"
    ],
    "unlinked_id_list": []
}