{
    "disease_id": "DOID:0070168",
    "recommended_name": {
        "id": "DOID:0070168",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070168",
        "name": "spermatogenic failure 3",
        "description": "A spermatogenic failure that is characterized by autosomal dominant inheritance of nonobstructive asthenozoospermia that has_material_basis_in heterozygous mutation in the SLC26A8 gene on chromosome 6p21."
    },
    "synonyms": [
        {
            "id": "DOID:0070168",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070168",
            "name": "SPGF3",
            "description": ""
        },
        {
            "id": "MONDO:0011720",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011720",
            "name": "spermatogenic failure 3",
            "description": "Any azoospermia in which the cause of the disease is a mutation in the SLC26A8 gene."
        },
        {
            "id": "MONDO:0011720",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011720",
            "name": "SLC26A8 azoospermia",
            "description": ""
        },
        {
            "id": "MONDO:0011720",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011720",
            "name": "azoospermia caused by mutation in SLC26A8",
            "description": ""
        },
        {
            "id": "MONDO:0011720",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011720",
            "name": "spermatogenic failure 3",
            "description": ""
        },
        {
            "id": "MONDO:0011720",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011720",
            "name": "spermatogenic failure type 3",
            "description": ""
        },
        {
            "id": "MONDO:0011720",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011720",
            "name": "SPGF3",
            "description": ""
        },
        {
            "id": "MIM:606766",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/606766",
            "name": "Spermatogenic failure 3",
            "description": "Spermatogenic failure 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070168"
    ],
    "unlinked_id_list": []
}