{
    "disease_id": "DOID:0080038", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009940", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009940", 
            "name": "Pyknodysostosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009940", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009940", 
            "name": "PKND"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009940", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009940", 
            "name": "Pycd"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080038", 
        "description": "An osteochondrodysplasia that has_material_basis_in a mutation in the CTSK gene which results_in dwarfism, brittle bones, osteopetrosis, shortening of the distal phalanges.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080038", 
        "name": "pycnodysostosis"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080038#disease-associations", 
            "id": "0080038", 
            "database": "Alliance of Genome Resources"
        }
    ]
}