{
    "disease_id": "DOID:0111851",
    "recommended_name": {
        "id": "DOID:0111851",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111851",
        "name": "primary ciliary dyskinesia 44",
        "description": "A primary ciliary dyskinesia characterized by recurrent sinopulmonary infections, defective mucociliary clearance, short respiratory epithelial cell motile cilia with decreased motility, and absence of situs inversus that has_material_basis_in homozygous or compound heterozygous mutation in the NEK10 gene on chromosome 3p24.1."
    },
    "synonyms": [
        {
            "id": "DOID:0111851",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111851",
            "name": "CILD44",
            "description": ""
        },
        {
            "id": "DOID:0111851",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111851",
            "name": "primary ciliary dyskinesia 44 without situs inversus",
            "description": ""
        },
        {
            "id": "MONDO:0032914",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032914",
            "name": "ciliary dyskinesia, primary, 44",
            "description": ""
        },
        {
            "id": "MONDO:0032914",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032914",
            "name": "CILD44",
            "description": ""
        },
        {
            "id": "MIM:618781",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618781",
            "name": "Ciliary dyskinesia, primary, 44",
            "description": "Ciliary dyskinesia, primary, 44"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111851"
    ],
    "unlinked_id_list": []
}