{
    "disease_id": "DOID:0070178",
    "recommended_name": {
        "id": "DOID:0070178",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070178",
        "name": "spermatogenic failure 10",
        "description": "A spermatogenic failure that is characterized by defects in the annulus or the ring-like structure located at the distal end of the flagellar midpiece the autosomal dominant inheritance of that has_material_basis_in mutation in the SEPT12 gene on chromosome 16p13."
    },
    "synonyms": [
        {
            "id": "DOID:0070178",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070178",
            "name": "SPGF10",
            "description": ""
        },
        {
            "id": "DOID:0070178",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070178",
            "name": "Spermatogenic failure with defective sperm annulus",
            "description": ""
        },
        {
            "id": "MONDO:0013901",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013901",
            "name": "spermatogenic failure 10",
            "description": "Any azoospermia in which the cause of the disease is a mutation in the SEPT12 gene."
        },
        {
            "id": "MONDO:0013901",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013901",
            "name": "SEPT12 azoospermia",
            "description": ""
        },
        {
            "id": "MONDO:0013901",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013901",
            "name": "azoospermia caused by mutation in SEPT12",
            "description": ""
        },
        {
            "id": "MONDO:0013901",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013901",
            "name": "spermatogenic failure 10",
            "description": ""
        },
        {
            "id": "MONDO:0013901",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013901",
            "name": "spermatogenic failure type 10",
            "description": ""
        },
        {
            "id": "MONDO:0013901",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013901",
            "name": "SPGF10",
            "description": ""
        },
        {
            "id": "MIM:614822",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614822",
            "name": "Spermatogenic failure 10",
            "description": "Spermatogenic failure 10"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070178"
    ],
    "unlinked_id_list": []
}