{
    "disease_id": "DOID:0110597",
    "recommended_name": {
        "id": "DOID:0110597",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110597",
        "name": "primary ciliary dyskinesia 22",
        "description": "A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer and inner dynein arm defect, recurrent respiratory infections, persistent rhinosinusitis, otitis media, chronic cough, variable presence of situs abnormalities, and has_material_basis_in homozygous or compound heterozygous mutation in the ZMYND10 gene on chromosome 3p21."
    },
    "synonyms": [
        {
            "id": "DOID:0110597",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110597",
            "name": "CILD22",
            "description": ""
        },
        {
            "id": "DOID:0110597",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110597",
            "name": "primary ciliary dyskinesia 22 with or without situs inversus",
            "description": ""
        },
        {
            "id": "MONDO:0014192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014192",
            "name": "primary ciliary dyskinesia 22",
            "description": "Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the ZMYND10 gene."
        },
        {
            "id": "MONDO:0014192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014192",
            "name": "CILD22",
            "description": ""
        },
        {
            "id": "MONDO:0014192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014192",
            "name": "ZMYND10 primary ciliary dyskinesia",
            "description": ""
        },
        {
            "id": "MONDO:0014192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014192",
            "name": "ciliary dyskinesia, primary, type 22",
            "description": ""
        },
        {
            "id": "MONDO:0014192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014192",
            "name": "primary ciliary dyskinesia caused by mutation in ZMYND10",
            "description": ""
        },
        {
            "id": "MONDO:0014192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014192",
            "name": "primary ciliary dyskinesia type 22",
            "description": ""
        },
        {
            "id": "MONDO:0014192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014192",
            "name": "ciliary dyskinesia, primary, 22",
            "description": ""
        },
        {
            "id": "MIM:615444",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615444",
            "name": "Ciliary dyskinesia, primary, 22",
            "description": "Ciliary dyskinesia, primary, 22"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110597"
    ],
    "unlinked_id_list": []
}