{
    "disease_id": "DOID:0111850", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010517", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010517", 
            "name": "ciliary dyskinesia, primary, 36, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010517", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010517", 
            "name": "ciliary dyskinesia, primary, 36, with or without situs inversus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010517", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010517", 
            "name": "PIH1D3 primary ciliary dyskinesia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010517", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010517", 
            "name": "primary ciliary dyskinesia caused by mutation in PIH1D3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010517", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010517", 
            "name": "CILD36"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010517", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010517", 
            "name": "ciliary dyskinesia, primary, 36, X-linked; CILD36"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111850", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111850", 
            "name": "CILD36"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111850", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111850", 
            "name": "X-linked primary ciliary dyskinesia 36"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111850", 
        "description": "A primary ciliary dyskinesia characterized by absence of outer dynein arms, defects in inner dynein arms, chronic airway disease and recurrent sinopulmonary infections, male infertility, and laterality defects in about half of patients that has_material_basis_in hemizygous mutation in PIH1D3 on chromosome Xq22.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111850", 
        "name": "primary ciliary dyskinesia 36"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111850#disease-associations", 
            "id": "0111850", 
            "database": "Alliance of Genome Resources"
        }
    ]
}