{
    "disease_id": "DOID:0080353",
    "recommended_name": {
        "id": "DOID:0080353",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080353",
        "name": "X-linked recessive hypophosphatemic rickets",
        "description": "A rickets that has_material_basis_in mutation in the CLCN5 gene on chromosome Xp11.22."
    },
    "synonyms": [
        {
            "id": "MONDO:0010358",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010358",
            "name": "hypophosphatemic rickets, X-linked recessive",
            "description": "Any X-linked hypophosphatemic rickets in which the cause of the disease is a mutation in the CLCN5 gene."
        },
        {
            "id": "MONDO:0010358",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010358",
            "name": "CLCN5 X-linked hypophosphatemic rickets",
            "description": ""
        },
        {
            "id": "MONDO:0010358",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010358",
            "name": "X-linked hypophosphatemic rickets caused by mutation in CLCN5",
            "description": ""
        },
        {
            "id": "MONDO:0010358",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010358",
            "name": "hypophosphatemic rickets, X-linked recessive",
            "description": ""
        },
        {
            "id": "MIM:300554",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300554",
            "name": "Hypophosphatemic rickets, X-linked recessive",
            "description": "Hypophosphatemic rickets, X-linked recessive"
        }
    ]
}