{
    "disease_id": "DOID:14213",
    "recommended_name": {
        "id": "DOID:14213",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:14213",
        "name": "hypophosphatasia",
        "description": "A syndrome characterized by disruption of mineralization of bones and teeth that has_material_basis_in mutation in ALPL on chromosome 1p36.12."
    },
    "synonyms": [
        {
            "id": "DOID:14213",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14213",
            "name": "childhood hypophosphatasia",
            "description": ""
        },
        {
            "id": "DOID:14213",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14213",
            "name": "deficiency of alkaline phosphatase",
            "description": ""
        },
        {
            "id": "DOID:14213",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14213",
            "name": "hypophospatasia, childhood",
            "description": ""
        }
    ]
}