{
    "disease_id": "DOID:0110627",
    "recommended_name": {
        "id": "DOID:0110627",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110627",
        "name": "primary ciliary dyskinesia 26",
        "description": "A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with inner and outer dynein arm defect, neonatal respiratory distress, recurrent upper and lower airway disease, bronchiectasis, and variable occurence of laterality defects and has_material_basis_in homozygous or compound heterozygous mutation in the C21ORF59 gene on chromosome 21q22."
    },
    "synonyms": [
        {
            "id": "DOID:0110627",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110627",
            "name": "CILD26",
            "description": ""
        },
        {
            "id": "DOID:0110627",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110627",
            "name": "primary ciliary dyskinesia 26 with or without situs inversus",
            "description": ""
        },
        {
            "id": "MONDO:0014211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014211",
            "name": "primary ciliary dyskinesia 26",
            "description": "Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the CFAP298 gene."
        },
        {
            "id": "MONDO:0014211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014211",
            "name": "CFAP298 primary ciliary dyskinesia",
            "description": ""
        },
        {
            "id": "MONDO:0014211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014211",
            "name": "CILD26",
            "description": ""
        },
        {
            "id": "MONDO:0014211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014211",
            "name": "ciliary dyskinesia, primary, type 26",
            "description": ""
        },
        {
            "id": "MONDO:0014211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014211",
            "name": "primary ciliary dyskinesia caused by mutation in CFAP298",
            "description": ""
        },
        {
            "id": "MONDO:0014211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014211",
            "name": "primary ciliary dyskinesia type 26",
            "description": ""
        },
        {
            "id": "MONDO:0014211",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014211",
            "name": "ciliary dyskinesia, primary, 26",
            "description": ""
        },
        {
            "id": "MIM:615500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615500",
            "name": "Ciliary dyskinesia, primary, 26",
            "description": "Ciliary dyskinesia, primary, 26"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110627"
    ],
    "unlinked_id_list": []
}