{
    "disease_id": "DOID:0110617", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012088", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012088", 
            "name": "primary ciliary dyskinesia type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012088", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012088", 
            "name": "CILD5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012088", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012088", 
            "name": "ciliary dyskinesia, primary, 5; CILD5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012088", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012088", 
            "name": "HYDIN primary ciliary dyskinesia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012088", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012088", 
            "name": "primary ciliary dyskinesia 5 without situs inversus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012088", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012088", 
            "name": "ciliary dyskinesia, primary, 5, without situs inversus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012088", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012088", 
            "name": "primary ciliary dyskinesia caused by mutation in HYDIN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012088", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012088", 
            "name": "ciliary dyskinesia, primary, type 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012088", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012088", 
            "name": "ciliary dyskinesia, primary, 5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110617", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110617", 
            "name": "CILD5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110617", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110617", 
            "name": "primary ciliary dyskinesia 5 without situs inversus"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110617", 
        "description": "A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with early onset of a progressive decline in lung function and has_material_basis_in homozygous mutation in the HYDIN gene on chromosome 16q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110617", 
        "name": "primary ciliary dyskinesia 5"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110617#disease-associations", 
            "id": "0110617", 
            "database": "Alliance of Genome Resources"
        }
    ]
}