{
    "disease_id": "DOID:0111732", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010803", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010803", 
            "name": "Eiken skeletal dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010803", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010803", 
            "name": "bone modeling defect of hands and feet"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111732", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111732", 
            "name": "Eiken skeletal dysplasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111732", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111732", 
            "name": "bone modeling defect of hands and feet"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111732", 
        "description": "A bone development disease characterized by severely delayed ossification primarily of the epiphyses, pelvis, hands, and feet and abnormal bone modeling of the hands and feet that has_material_basis_in homozygous or compound heterozygous mutation in PTHR1 on chromosome 3p21.31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111732", 
        "name": "Eiken syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111732#disease-associations", 
            "id": "0111732", 
            "database": "Alliance of Genome Resources"
        }
    ]
}