{
    "disease_id": "DOID:0110608", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013979", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013979", 
            "name": "CILD19"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013979", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013979", 
            "name": "ciliary dyskinesia, primary, type 19"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013979", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013979", 
            "name": "primary ciliary dyskinesia type 19"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013979", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013979", 
            "name": "primary ciliary dyskinesia caused by mutation in LRRC6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013979", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013979", 
            "name": "ciliary dyskinesia, primary, 19; CILD19"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013979", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013979", 
            "name": "ciliary dyskinesia, primary, 19"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013979", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013979", 
            "name": "primary ciliary dyskinesia 19 with or without situs inversus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013979", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013979", 
            "name": "ciliary dyskinesia, primary, 19, with or without situs inversus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013979", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013979", 
            "name": "LRRC6 primary ciliary dyskinesia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110608", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110608", 
            "name": "CILD19"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110608", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110608", 
            "name": "primary ciliary dyskinesia 19 with or without situs inversus"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110608", 
        "description": "A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer and inner dynein arm defect, chronic sinopulmonary infections, asthenospermia, and immotile cilia and has_material_basis_in homozygous mutation in the LRRC6 on chromosome 8q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110608", 
        "name": "primary ciliary dyskinesia 19"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110608#disease-associations", 
            "id": "0110608", 
            "database": "Alliance of Genome Resources"
        }
    ]
}