{
    "disease_id": "DOID:0110625", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014030", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014030", 
            "name": "primary ciliary dyskinesia type 20"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014030", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014030", 
            "name": "CCDC114 primary ciliary dyskinesia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014030", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014030", 
            "name": "ciliary dyskinesia, primary, 20"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014030", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014030", 
            "name": "primary ciliary dyskinesia 20 with or without situs inversus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014030", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014030", 
            "name": "CILD20"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014030", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014030", 
            "name": "ciliary dyskinesia, primary, 20, with or without situs inversus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014030", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014030", 
            "name": "primary ciliary dyskinesia caused by mutation in CCDC114"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014030", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014030", 
            "name": "ciliary dyskinesia, primary, 20; CILD20"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014030", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014030", 
            "name": "ciliary dyskinesia, primary, type 20"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110625", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110625", 
            "name": "CILD20"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110625", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110625", 
            "name": "primary ciliary dyskinesia 20 with or without situs inversus"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110625", 
        "description": "A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer dynein arm defect, infantile onset of chronic sinopulmonary infections, and variable occurence of laterality defects and has_material_basis_in homozygous or compound heterozygous mutation in the CCDC114 gene on chromosome 19q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110625", 
        "name": "primary ciliary dyskinesia 20"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110625#disease-associations", 
            "id": "0110625", 
            "database": "Alliance of Genome Resources"
        }
    ]
}