{
    "disease_id": "DOID:0110622",
    "recommended_name": {
        "id": "DOID:0110622",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110622",
        "name": "primary ciliary dyskinesia 9",
        "description": "A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer dynein arm defect, neonatal respiratory distress, sinusitis, otitis, bronchiectasis, and variable occurence of laterality defects and has_material_basis_in homozygous mutation in the DNAI2 gene on chromosome 17q25."
    },
    "synonyms": [
        {
            "id": "DOID:0110622",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110622",
            "name": "CILD9",
            "description": ""
        },
        {
            "id": "DOID:0110622",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110622",
            "name": "primary ciliary dyskinesia 9 with or without situs inversus",
            "description": ""
        },
        {
            "id": "MONDO:0012906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012906",
            "name": "primary ciliary dyskinesia 9",
            "description": "Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the DNAI2 gene."
        },
        {
            "id": "MONDO:0012906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012906",
            "name": "ciliary dyskinesia, primary, type 9",
            "description": ""
        },
        {
            "id": "MONDO:0012906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012906",
            "name": "CILD9",
            "description": ""
        },
        {
            "id": "MONDO:0012906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012906",
            "name": "ciliary dyskinesia, primary, 9",
            "description": ""
        },
        {
            "id": "MONDO:0012906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012906",
            "name": "DNAI2 primary ciliary dyskinesia",
            "description": ""
        },
        {
            "id": "MONDO:0012906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012906",
            "name": "primary ciliary dyskinesia caused by mutation in DNAI2",
            "description": ""
        },
        {
            "id": "MONDO:0012906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012906",
            "name": "primary ciliary dyskinesia 9 with or without situs inversus",
            "description": ""
        },
        {
            "id": "MONDO:0012906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012906",
            "name": "ciliary dyskinesia, primary, 9, with or without situs inversus",
            "description": ""
        },
        {
            "id": "MONDO:0012906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012906",
            "name": "primary ciliary dyskinesia type 9",
            "description": ""
        },
        {
            "id": "MONDO:0012906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012906",
            "name": "ciliary dyskinesia, primary, 9; CILD9",
            "description": ""
        },
        {
            "id": "MIM:612444",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612444",
            "name": "Ciliary dyskinesia, primary, 9",
            "description": "Ciliary dyskinesia, primary, 9"
        }
    ]
}