{
    "disease_id": "DOID:0070577",
    "recommended_name": {
        "id": "DOID:0070577",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070577",
        "name": "spermatogenic failure 78",
        "description": "A spermatogenic failure characterized by sperm with abnormal acrosome structure due to a manchette assembly defect that has_material_basis_in homozygous mutation in the IQCN gene on chromosome 19p13.11."
    },
    "synonyms": [
        {
            "id": "DOID:0070577",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070577",
            "name": "SPGF78",
            "description": ""
        },
        {
            "id": "MONDO:0859338",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0859338",
            "name": "spermatogenic failure 78",
            "description": ""
        },
        {
            "id": "MIM:620170",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620170",
            "name": "Spermatogenic failure 78",
            "description": "Spermatogenic failure 78"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070577"
    ],
    "unlinked_id_list": []
}