{
    "disease_id": "DOID:0110603",
    "recommended_name": {
        "id": "DOID:0110603",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110603",
        "name": "primary ciliary dyskinesia 32",
        "description": "A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with near absence of radial spokes, respiratory distress in term neonates, impaired mucociliary clearance, chronic respiratory infections, bronchiectasis, and infertility and has_material_basis_in homozygous or compound heterozygous mutation in the RSPH3 gene on chromosome 6q25."
    },
    "synonyms": [
        {
            "id": "DOID:0110603",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110603",
            "name": "CILD32",
            "description": ""
        },
        {
            "id": "DOID:0110603",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110603",
            "name": "primary ciliary dyskinesia 32 without situs inversus",
            "description": ""
        },
        {
            "id": "MONDO:0014657",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014657",
            "name": "primary ciliary dyskinesia 32",
            "description": "Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the RSPH3 gene."
        },
        {
            "id": "MONDO:0014657",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014657",
            "name": "CILD32",
            "description": ""
        },
        {
            "id": "MONDO:0014657",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014657",
            "name": "RSPH3 primary ciliary dyskinesia",
            "description": ""
        },
        {
            "id": "MONDO:0014657",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014657",
            "name": "ciliary dyskinesia, primary, type 32",
            "description": ""
        },
        {
            "id": "MONDO:0014657",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014657",
            "name": "primary ciliary dyskinesia caused by mutation in RSPH3",
            "description": ""
        },
        {
            "id": "MONDO:0014657",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014657",
            "name": "primary ciliary dyskinesia type 32",
            "description": ""
        },
        {
            "id": "MONDO:0014657",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014657",
            "name": "ciliary dyskinesia, primary, 32",
            "description": ""
        },
        {
            "id": "MIM:616481",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616481",
            "name": "Ciliary dyskinesia, primary, 32",
            "description": "Ciliary dyskinesia, primary, 32"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110603"
    ],
    "unlinked_id_list": []
}