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