{
    "disease_id": "DOID:0110623",
    "recommended_name": {
        "id": "DOID:0110623",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110623",
        "name": "primary ciliary dyskinesia 15",
        "description": "A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with inner dynein arm defect, axonemal disorganization, recurrent respiratory infections and has_material_basis_in homozygous or compound heterozygous mutation in the CCDC40 gene on chromosome 17q25."
    },
    "synonyms": [
        {
            "id": "DOID:0110623",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110623",
            "name": "primary ciliary dyskinesia 15 with or without situs inversus",
            "description": ""
        },
        {
            "id": "DOID:0110623",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110623",
            "name": "CILD15",
            "description": ""
        },
        {
            "id": "MONDO:0013435",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013435",
            "name": "primary ciliary dyskinesia 15",
            "description": "Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the CCDC40 gene."
        },
        {
            "id": "MONDO:0013435",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013435",
            "name": "CCDC40 primary ciliary dyskinesia",
            "description": ""
        },
        {
            "id": "MONDO:0013435",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013435",
            "name": "CILD15",
            "description": ""
        },
        {
            "id": "MONDO:0013435",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013435",
            "name": "ciliary dyskinesia, primary, type 15",
            "description": ""
        },
        {
            "id": "MONDO:0013435",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013435",
            "name": "primary ciliary dyskinesia 15",
            "description": ""
        },
        {
            "id": "MONDO:0013435",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013435",
            "name": "primary ciliary dyskinesia 15 with or without situs inversus",
            "description": ""
        },
        {
            "id": "MONDO:0013435",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013435",
            "name": "primary ciliary dyskinesia caused by mutation in CCDC40",
            "description": ""
        },
        {
            "id": "MONDO:0013435",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013435",
            "name": "primary ciliary dyskinesia type 15",
            "description": ""
        },
        {
            "id": "MONDO:0013435",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013435",
            "name": "ciliary dyskinesia, primary, 15",
            "description": ""
        },
        {
            "id": "MONDO:0013435",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013435",
            "name": "ciliary dyskinesia, primary, 15, with or without situs inversus",
            "description": ""
        },
        {
            "id": "MIM:613808",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613808",
            "name": "Ciliary dyskinesia, primary, 15",
            "description": "Ciliary dyskinesia, primary, 15"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110623"
    ],
    "unlinked_id_list": []
}