{
    "disease_id": "DOID:0110626", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011718", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011718", 
            "name": "ciliary dyskinesia, primary, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011718", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011718", 
            "name": "primary ciliary dyskinesia caused by mutation in DNAAF3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011718", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011718", 
            "name": "primary ciliary dyskinesia 2 with or without situs inversus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011718", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011718", 
            "name": "ciliary dyskinesia, primary, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011718", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011718", 
            "name": "ciliary dyskinesia, primary, 2; CILD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011718", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011718", 
            "name": "CILD2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011718", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011718", 
            "name": "ciliary dyskinesia, primary, 2, with or without situs inversus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011718", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011718", 
            "name": "DNAAF3 primary ciliary dyskinesia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011718", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011718", 
            "name": "primary ciliary dyskinesia type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110626", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110626", 
            "name": "primary ciliary dyskinesia 2 with or without situs inversus"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110626", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110626", 
            "name": "CILD2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110626", 
        "description": "A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with inner and outer dynein arm defect, otitis media, sinusitis, chronic cough, recurrent respiratory infections, and variable occurence of laterality defects and has_material_basis_in homozygous mutation in the DNAAF3 gene on chromosome 19q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110626", 
        "name": "primary ciliary dyskinesia 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110626#disease-associations", 
            "id": "0110626", 
            "database": "Alliance of Genome Resources"
        }
    ]
}