{
    "disease_id": "DOID:0112176",
    "recommended_name": {
        "id": "DOID:0112176",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0112176",
        "name": "spermatogenic failure 48",
        "description": "A spermatogenic failure that is characterized by impaired spermatogenesis, primarily occurring at meiosis that has_material_basis_in homozygous or compound heterozygous mutation in M1AP on chromosome 2p13.1."
    },
    "synonyms": [
        {
            "id": "DOID:0112176",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112176",
            "name": "SPGF48",
            "description": ""
        },
        {
            "id": "MONDO:0030846",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030846",
            "name": "spermatogenic failure 48",
            "description": ""
        },
        {
            "id": "MONDO:0030846",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030846",
            "name": "SPGF48",
            "description": ""
        },
        {
            "id": "MONDO:0030846",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030846",
            "name": "spermatogenic failure 48",
            "description": ""
        },
        {
            "id": "MIM:619108",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619108",
            "name": "Spermatogenic failure 48",
            "description": "Spermatogenic failure 48"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112176"
    ],
    "unlinked_id_list": []
}