{
    "disease_id": "DOID:0110618", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013174", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013174", 
            "name": "primary ciliary dyskinesia type 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013174", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013174", 
            "name": "ciliary dyskinesia, primary, 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013174", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013174", 
            "name": "primary ciliary dyskinesia caused by mutation in DNAAF1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013174", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013174", 
            "name": "primary ciliary dyskinesia 13 with or without situs inversus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013174", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013174", 
            "name": "ciliary dyskinesia, primary, 13, with or without situs inversus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013174", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013174", 
            "name": "DNAAF1 primary ciliary dyskinesia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013174", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013174", 
            "name": "ciliary dyskinesia, primary, 13; CILD13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013174", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013174", 
            "name": "CILD13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013174", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013174", 
            "name": "ciliary dyskinesia, primary, type 13"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110618", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110618", 
            "name": "CILD13"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110618", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110618", 
            "name": "primary ciliary dyskinesia 13 with or without situs inversus"
        }, 
        {
            "url": "https://www.omim.org/entry/613193", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:613193", 
            "name": "Ciliary dyskinesia, primary, 13"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110618", 
        "description": "A primary ciliary dyskinesia that is characterized by inner and outer dynein arm defect, immotile cilia, and variable occurence of laterality defects and has_material_basis_in homozygous or compound heterozygous mutation in the LRRC50 gene on chromosome 16q23-q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110618", 
        "name": "primary ciliary dyskinesia 13"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613193", 
            "id": "613193", 
            "database": "MIM"
        }
    ]
}