{"Name":"Multicentric osteolysis nodulosis arthropathy spectrum","DiseaseID__c":"GARD:0017610","id":17610,"encodedName":"multicentric-osteolysis-nodulosis-arthropathy-spectrum","IsDeleted":false,"Disease_Name_Full__c":"Multicentric osteolysis nodulosis arthropathy spectrum","Xref_IDs__c":"716868003; C123437; C1850155; MEDGEN:342428; MONDO:0018298; ORPHA:371428","USA_Estimate__c":null,"No_of_Specialist_Tagsa__c":3,"No_of_ClinGen_records__c":0,"No_of_GeneReviews__c":0,"No_of_HHS_records__c":1,"World_Estimate__c":null,"No_of_HRSA_records__c":0,"Evidence_Based_Score__c":1,"No_of_Disease_Descriptions__c":3,"Disease_Characteristics_Score__c":6,"No_of_Age_at_Onset__c":2,"Description_Source__c":"MONDO:0018298","Disease_Description__c":"A rare systemic or rheumatologic disease characterized by peripheral osteolysis (especially carpal and tarsal bones), interphalangeal joint erosions, subcutaneous fibrocollagenous nodules, facial dysmorphism, and a wide range of associated manifestations.","GARD_Name__c":"Multicentric osteolysis nodulosis arthropathy spectrum","GARD_Synonym__c":"mona (multicentric osteolysis nodulosis arthropathy) spectrum; 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