{
    "disease_id": "DOID:0110617",
    "recommended_name": {
        "id": "DOID:0110617",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110617",
        "name": "primary ciliary dyskinesia 5",
        "description": "A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with early onset of a progressive decline in lung function and has_material_basis_in homozygous mutation in the HYDIN gene on chromosome 16q22."
    },
    "synonyms": [
        {
            "id": "DOID:0110617",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110617",
            "name": "CILD5",
            "description": ""
        },
        {
            "id": "DOID:0110617",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110617",
            "name": "primary ciliary dyskinesia 5 without situs inversus",
            "description": ""
        },
        {
            "id": "MONDO:0012088",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012088",
            "name": "primary ciliary dyskinesia 5",
            "description": "Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the HYDIN gene."
        },
        {
            "id": "MONDO:0012088",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012088",
            "name": "CILD5",
            "description": ""
        },
        {
            "id": "MONDO:0012088",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012088",
            "name": "HYDIN primary ciliary dyskinesia",
            "description": ""
        },
        {
            "id": "MONDO:0012088",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012088",
            "name": "ciliary dyskinesia, primary, type 5",
            "description": ""
        },
        {
            "id": "MONDO:0012088",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012088",
            "name": "primary ciliary dyskinesia caused by mutation in HYDIN",
            "description": ""
        },
        {
            "id": "MONDO:0012088",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012088",
            "name": "primary ciliary dyskinesia type 5",
            "description": ""
        },
        {
            "id": "MONDO:0012088",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012088",
            "name": "ciliary dyskinesia, primary, 5",
            "description": ""
        },
        {
            "id": "MIM:608647",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/608647",
            "name": "Ciliary dyskinesia, primary, 5",
            "description": "Ciliary dyskinesia, primary, 5"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110617"
    ],
    "unlinked_id_list": []
}