{
    "disease_id": "DOID:0111930",
    "recommended_name": {
        "id": "DOID:0111930",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111930",
        "name": "spermatogenic failure 29",
        "description": "A spermatogenic failure characterized by nonobstructive azoospermia or oligozoospermia, immotile sperm, and sperm acrosome and head-neck junction abnormalities that has_material_basis_in homozygous or compound geterozygous mutation in SPINK2 on chromosome 4q12."
    },
    "synonyms": [
        {
            "id": "DOID:0111930",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111930",
            "name": "SPGF29",
            "description": ""
        },
        {
            "id": "MONDO:0054733",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054733",
            "name": "spermatogenic failure 29",
            "description": ""
        },
        {
            "id": "MONDO:0054733",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054733",
            "name": "spermatogenic failure 29; SPGF29",
            "description": ""
        },
        {
            "id": "MONDO:0054733",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0054733",
            "name": "SPGF29",
            "description": ""
        },
        {
            "id": "MIM:618091",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618091",
            "name": "Spermatogenic failure 29",
            "description": "Spermatogenic failure 29"
        }
    ]
}