{
    "disease_id": "DOID:0111858",
    "recommended_name": {
        "id": "DOID:0111858",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111858",
        "name": "primary ciliary dyskinesia 41",
        "description": "A primary ciliary dyskinesia characterized by hyperkinetic ciliary beat patterns, defects in ciliary orientation, chronic sinusitis, otitis media, and bronchiectasis that has_material_basis_in homozygous or compound heterozygous mutation in the GAS2L2 gene on chromosome 17q12."
    },
    "synonyms": [
        {
            "id": "DOID:0111858",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111858",
            "name": "CILD41",
            "description": ""
        },
        {
            "id": "MONDO:0032757",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032757",
            "name": "ciliary dyskinesia, primary, 41",
            "description": ""
        },
        {
            "id": "MONDO:0032757",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032757",
            "name": "CILD41",
            "description": ""
        },
        {
            "id": "MIM:618449",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618449",
            "name": "Ciliary dyskinesia, primary, 41",
            "description": "Ciliary dyskinesia, primary, 41"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111858"
    ],
    "unlinked_id_list": []
}