{
    "disease_id": "DOID:0110603", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014657", 
            "name": "ciliary dyskinesia, primary, 32, without situs inversus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014657", 
            "name": "RSPH3 primary ciliary dyskinesia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014657", 
            "name": "ciliary dyskinesia, primary, 32; CILD32"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014657", 
            "name": "ciliary dyskinesia, primary, type 32"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014657", 
            "name": "primary ciliary dyskinesia caused by mutation in RSPH3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014657", 
            "name": "primary ciliary dyskinesia 32 without situs inversus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014657", 
            "name": "ciliary dyskinesia, primary, 32"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014657", 
            "name": "primary ciliary dyskinesia type 32"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014657", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014657", 
            "name": "CILD32"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110603", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110603", 
            "name": "CILD32"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110603", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110603", 
            "name": "primary ciliary dyskinesia 32 without situs inversus"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110603", 
        "description": "A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with near absence of radial spokes, respiratory distress in term neonates, impaired mucociliary clearance, chronic respiratory infections, bronchiectasis, and infertility and has_material_basis_in homozygous or compound heterozygous mutation in the RSPH3 gene on chromosome 6q25.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110603", 
        "name": "primary ciliary dyskinesia 32"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110603#disease-associations", 
            "id": "0110603", 
            "database": "Alliance of Genome Resources"
        }
    ]
}