{
    "disease_id": "DOID:0110613",
    "recommended_name": {
        "id": "DOID:0110613",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110613",
        "name": "primary ciliary dyskinesia 16",
        "description": "A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with absence of ciliary outer dynein arms, early infantile onset of respiratory distress, and variable occurrence of situs inversus and has_material_basis_in homozygous mutation in the DNAL1 gene on chromosome 14q24.3."
    },
    "synonyms": [
        {
            "id": "DOID:0110613",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110613",
            "name": "primary ciliary dyskinesia 16 with or without situs inversus",
            "description": ""
        },
        {
            "id": "DOID:0110613",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110613",
            "name": "CILD16",
            "description": ""
        },
        {
            "id": "MONDO:0013525",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013525",
            "name": "primary ciliary dyskinesia 16",
            "description": "Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the DNAL1 gene."
        },
        {
            "id": "MONDO:0013525",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013525",
            "name": "CILD16",
            "description": ""
        },
        {
            "id": "MONDO:0013525",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013525",
            "name": "DNAL1 primary ciliary dyskinesia",
            "description": ""
        },
        {
            "id": "MONDO:0013525",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013525",
            "name": "ciliary dyskinesia, primary, type 16",
            "description": ""
        },
        {
            "id": "MONDO:0013525",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013525",
            "name": "primary ciliary dyskinesia caused by mutation in DNAL1",
            "description": ""
        },
        {
            "id": "MONDO:0013525",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013525",
            "name": "primary ciliary dyskinesia type 16",
            "description": ""
        },
        {
            "id": "MONDO:0013525",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013525",
            "name": "ciliary dyskinesia, primary, 16",
            "description": ""
        },
        {
            "id": "MIM:614017",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614017",
            "name": "Ciliary dyskinesia, primary, 16",
            "description": "Ciliary dyskinesia, primary, 16"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110613"
    ],
    "unlinked_id_list": []
}