{
    "disease_id": "DOID:0070181",
    "recommended_name": {
        "id": "DOID:0070181",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070181",
        "name": "spermatogenic failure 23",
        "description": "An azoospermia characterized by autosomal recessive inhertitance of nonobstructive azoospermia that has_material_basis_in mutation in the TEX14 gene on chromosome 17q23."
    },
    "synonyms": [
        {
            "id": "DOID:0070181",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070181",
            "name": "SPGF23",
            "description": ""
        },
        {
            "id": "MONDO:0054727",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054727",
            "name": "spermatogenic failure 23",
            "description": ""
        },
        {
            "id": "MONDO:0054727",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054727",
            "name": "SPGF23",
            "description": ""
        },
        {
            "id": "MONDO:0054727",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054727",
            "name": "spermatogenic failure 23; SPGF23",
            "description": ""
        },
        {
            "id": "MIM:617707",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617707",
            "name": "Spermatogenic failure 23",
            "description": "Spermatogenic failure 23"
        }
    ]
}