{
    "disease_id": "DOID:0110627", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014211", 
            "name": "primary ciliary dyskinesia caused by mutation in CFAP298"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014211", 
            "name": "ciliary dyskinesia, primary, 26"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014211", 
            "name": "ciliary dyskinesia, primary, 26; CILD26"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014211", 
            "name": "ciliary dyskinesia, primary, 26, with or without situs inversus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014211", 
            "name": "CILD26"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014211", 
            "name": "primary ciliary dyskinesia type 26"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014211", 
            "name": "CFAP298 primary ciliary dyskinesia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014211", 
            "name": "ciliary dyskinesia, primary, type 26"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014211", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014211", 
            "name": "primary ciliary dyskinesia 26 with or without situs inversus"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110627", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110627", 
            "name": "CILD26"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110627", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110627", 
            "name": "primary ciliary dyskinesia 26 with or without situs inversus"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110627", 
        "description": "A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with inner and outer dynein arm defect, neonatal respiratory distress, recurrent upper and lower airway disease, bronchiectasis, and variable occurence of laterality defects and has_material_basis_in homozygous or compound heterozygous mutation in the C21ORF59 gene on chromosome 21q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110627", 
        "name": "primary ciliary dyskinesia 26"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110627#disease-associations", 
            "id": "0110627", 
            "database": "Alliance of Genome Resources"
        }
    ]
}