{
    "disease_id": "DOID:0110620",
    "recommended_name": {
        "id": "DOID:0110620",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110620",
        "name": "primary ciliary dyskinesia 35",
        "description": "A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with absent outer dynein arms, immotile cilia, variable occurence of laterality defects and recurrent upper and lower respiratory infections and has_material_basis_in homozygous mutation in the TTC25 gene on chromosome 17q21."
    },
    "synonyms": [
        {
            "id": "DOID:0110620",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110620",
            "name": "primary ciliary dyskinesia 35 with or without situs inversus",
            "description": ""
        },
        {
            "id": "DOID:0110620",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110620",
            "name": "CILD35",
            "description": ""
        },
        {
            "id": "MONDO:0014910",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014910",
            "name": "primary ciliary dyskinesia 35",
            "description": "Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the TTC25 gene."
        },
        {
            "id": "MONDO:0014910",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014910",
            "name": "CILD35",
            "description": ""
        },
        {
            "id": "MONDO:0014910",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014910",
            "name": "TTC25 primary ciliary dyskinesia",
            "description": ""
        },
        {
            "id": "MONDO:0014910",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014910",
            "name": "ciliary dyskinesia, primary, 35",
            "description": ""
        },
        {
            "id": "MONDO:0014910",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014910",
            "name": "ciliary dyskinesia, primary, type 35",
            "description": ""
        },
        {
            "id": "MONDO:0014910",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014910",
            "name": "primary ciliary dyskinesia caused by mutation in TTC25",
            "description": ""
        },
        {
            "id": "MONDO:0014910",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014910",
            "name": "primary ciliary dyskinesia type 35",
            "description": ""
        },
        {
            "id": "MIM:617092",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617092",
            "name": "Ciliary dyskinesia, primary, 35",
            "description": "Ciliary dyskinesia, primary, 35"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110620"
    ],
    "unlinked_id_list": []
}