{
    "disease_id": "DOID:0111512", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007979", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007979", 
            "name": "METCDS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007979", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007979", 
            "name": "METACHONDROMATOSIS; METCDS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111512", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111512", 
            "name": "METCDS"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111512", 
        "description": "An osteochondrodysplasia characterized by the presence of both multiple multiple enchondromas and exostoses that has_material_basis_in heterozygous mutation in PTPN11 on chromosome 12q24.13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111512", 
        "name": "metachondromatosis"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111512#disease-associations", 
            "id": "0111512", 
            "database": "Alliance of Genome Resources"
        }
    ]
}