{
    "disease_id": "DOID:0080353", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010358", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010358", 
            "name": "hypophosphatemic rickets, X-linked recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010358", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010358", 
            "name": "X-linked hypophosphatemic rickets caused by mutation in CLCN5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010358", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010358", 
            "name": "CLCN5 X-linked hypophosphatemic rickets"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080353", 
        "description": "A rickets that has_material_basis_in mutation in the CLCN5 gene on chromosome Xp11.22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080353", 
        "name": "X-linked recessive hypophosphatemic rickets"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080353#disease-associations", 
            "id": "0080353", 
            "database": "Alliance of Genome Resources"
        }
    ]
}