{
    "disease_id": "DOID:0111534", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008152", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008152", 
            "name": "multicentric carpo-tarsal osteolysis with or without nephropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008152", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008152", 
            "name": "multicentric osteolysis nephropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008152", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008152", 
            "name": "Carnevale canun Mendoza syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008152", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008152", 
            "name": "MCTO"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008152", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008152", 
            "name": "idiopathic multicentric osteolysis with or without nephropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008152", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008152", 
            "name": "multicentric carpotarsal osteolysis syndrome; MCTO"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008152", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008152", 
            "name": "osteolysis, hereditary, of carpal bones with or without nephropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008152", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008152", 
            "name": "multicentric osteolysis, autosomal dominant"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111534", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111534", 
            "name": "idiopathic multicentric osteolysis with or without nephropathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111534", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111534", 
            "name": "MCTO"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111534", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111534", 
            "name": "autosomal dominant multicentric osteolysis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111534", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111534", 
            "name": "multicentric osteolysis nephropathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111534", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111534", 
            "name": "multicentric carpo-tarsal osteolysis with or without nephropathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111534", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111534", 
            "name": "hereditary osteolysis of carpal bones with or without nephropathy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111534", 
        "description": "A syndrome characterized by progressive loss of bone, typically involving the capsal and tarsal bones, and in many cases chronic renal failure that has_material_basis_in heterozygous mutation in MAFB on chromosome 20q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111534", 
        "name": "multicentric carpotarsal osteolysis syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111534#disease-associations", 
            "id": "0111534", 
            "database": "Alliance of Genome Resources"
        }
    ]
}