{
    "disease_id": "DOID:0111929", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054728", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054728", 
            "name": "SPGF24"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0054728", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0054728", 
            "name": "spermatogenic failure 24; SPGF24"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111929", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111929", 
            "name": "SPGF24"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111929", 
        "description": "A spermatogenic failure characterized by multiple morphologic abnormalities of the flagella, malformed sperm heads, and very low sperm counts that has_material_basis_in homozygous or compound heterozygous mutation in CFAP69 on chromosome 7q21.13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111929", 
        "name": "spermatogenic failure 24"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/617959", 
            "id": "617959", 
            "database": "MIM"
        }
    ]
}