{
    "disease_id": "DOID:0110608",
    "recommended_name": {
        "id": "DOID:0110608",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110608",
        "name": "primary ciliary dyskinesia 19",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0110608",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110608",
            "name": "CILD19",
            "description": ""
        },
        {
            "id": "DOID:0110608",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110608",
            "name": "primary ciliary dyskinesia 19 with or without situs inversus",
            "description": ""
        },
        {
            "id": "MONDO:0013979",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013979",
            "name": "primary ciliary dyskinesia 19",
            "description": "Any primary ciliary dyskinesia in which the cause of the disease is a mutation in the LRRC6 gene."
        },
        {
            "id": "MONDO:0013979",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013979",
            "name": "CILD19",
            "description": ""
        },
        {
            "id": "MONDO:0013979",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013979",
            "name": "ciliary dyskinesia, primary, type 19",
            "description": ""
        },
        {
            "id": "MONDO:0013979",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013979",
            "name": "primary ciliary dyskinesia type 19",
            "description": ""
        },
        {
            "id": "MONDO:0013979",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013979",
            "name": "primary ciliary dyskinesia caused by mutation in LRRC6",
            "description": ""
        },
        {
            "id": "MONDO:0013979",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013979",
            "name": "ciliary dyskinesia, primary, 19; CILD19",
            "description": ""
        },
        {
            "id": "MONDO:0013979",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013979",
            "name": "ciliary dyskinesia, primary, 19",
            "description": ""
        },
        {
            "id": "MONDO:0013979",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013979",
            "name": "primary ciliary dyskinesia 19 with or without situs inversus",
            "description": ""
        },
        {
            "id": "MONDO:0013979",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013979",
            "name": "ciliary dyskinesia, primary, 19, with or without situs inversus",
            "description": ""
        },
        {
            "id": "MONDO:0013979",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013979",
            "name": "LRRC6 primary ciliary dyskinesia",
            "description": ""
        },
        {
            "id": "MIM:614935",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614935",
            "name": "Ciliary dyskinesia, primary, 19",
            "description": "Ciliary dyskinesia, primary, 19"
        }
    ]
}