{"Name":"Mosaic trisomy 13","DiseaseID__c":"GARD:0010869","id":10869,"encodedName":"mosaic-trisomy-13","IsDeleted":false,"Disease_Name_Full__c":"Mosaic trisomy 13","Xref_IDs__c":"CN306867; MEDGEN:990817; MONDO:0700034","USA_Estimate__c":null,"No_of_Specialist_Tagsa__c":1,"No_of_ClinGen_records__c":0,"No_of_GeneReviews__c":0,"No_of_HHS_records__c":0,"World_Estimate__c":null,"No_of_HRSA_records__c":0,"Evidence_Based_Score__c":0,"No_of_Disease_Descriptions__c":1,"Disease_Characteristics_Score__c":3,"No_of_Age_at_Onset__c":0,"Description_Source__c":"MONDO:0700034","Disease_Description__c":"Trisomy 13 in which the presence of an extra copy of chromosome 13 is present only in some of the cells of the organism.","GARD_Name__c":"Mosaic trisomy 13","GARD_Synonym__c":"trisomy 13 mosaicism","Curated_Disease_Description_Source__c":"MONDO:0700034","Curated_Disease_Description__c":"Trisomy 13 in which the presence of an extra copy of chromosome 13 is present only in some of the cells of the organism.","Curated_USA_Estimate_Source__c":null,"Curated_USA_Estimate__c":null,"Age_at_Onset_Snippet_Text__c":null,"SourceID__c":null,"Deprecated__c":"No","Disease_Concept_Type__c":"Rare Disease Entity","MONDO_ID__c":"MONDO:0700034","ORPHANET_ID__c":null,"Replaced_By_ID__c":null,"Display_Spanish_Disease_Name__c":null,"Spanish_Description_Source__c":null,"Spanish_Description__c":null,"Spanish_Disease_Name__c":null,"Spanish_GARD_Synonym__c":null,"Category_Linearization__c":null,"icd10_id__c":null,"mesh_id__c":null,"omim_id__c":null,"snomed_id__c":null,"umls_id__c":null,"GARD_Disease__c":[{"Curated_Disease_Description__c":"Trisomy 13 in which the presence of an extra copy of chromosome 13 is present only in some of the cells of the organism.","Curated_Disease_Description_Source__c":"MONDO:0700034","GARD_Synonym__c":"trisomy 13 mosaicism","Name":"Mosaic trisomy 13","estimateUsa":""}],"Organization_Supported_Diseases__c":[{"Account_Name__c":"Chromosome Disorder Outreach","Website__c":"https://chromodisorder.org/"},{"Account_Name__c":"Unique","Website__c":"https://rarechromo.org/"},{"Account_Name__c":"Support Organization for Trisomy 18, 13, and Related Disorders","Website__c":"https://trisomy.org/"},{"Account_Name__c":"Hope For Trisomy","Website__c":"https://www.hopefortrisomy13and18.org/"}],"GARD_Disease_Tag__c":[{"Tag_Name__c":"Retinal","Tag_Category__c":"Account;Specialist","curated_tag_name":"Retinal disorders"}],"External_Identifier_Disease__c":[{"URL__c":"https://www.ncbi.nlm.nih.gov/medgen/?term=990817","Source__c":"CN306867","Xref__c":"MEDGEN:990817"},{"URL__c":"https://uts.nlm.nih.gov/uts/umls/concept/CN306867","Source__c":"CN306867","Xref__c":"CN306867"},{"URL__c":"http://purl.obolibrary.org/obo/MONDO_0700034","Source__c":"GARD:0010869","Xref__c":"MONDO:0700034"}],"tags":{"Account":["Retinal"],"Specialist":["Retinal"]},"synonyms":["trisomy 13 mosaicism"]}