{"Name":"Sacral hemangiomas multiple congenital abnormalities","DiseaseID__c":"GARD:0000317","id":317,"encodedName":"sacral-hemangiomas-multiple-congenital-abnormalities","IsDeleted":false,"Disease_Name_Full__c":"Sacral hemangiomas multiple congenital abnormalities","Xref_IDs__c":"C2931443; C537222; MEDGEN:419414; MONDO:0042961","USA_Estimate__c":null,"No_of_Specialist_Tagsa__c":0,"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":0,"Disease_Characteristics_Score__c":1,"No_of_Age_at_Onset__c":0,"Description_Source__c":"MEDGEN:C2931443","Disease_Description__c":null,"GARD_Name__c":"Sacral hemangiomas multiple congenital abnormalities","GARD_Synonym__c":null,"Curated_Disease_Description_Source__c":"MEDGEN:C2931443","Curated_Disease_Description__c":null,"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:0042961","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_Source__c":"MEDGEN:C2931443","Name":"Sacral hemangiomas multiple congenital abnormalities","estimateUsa":""}],"External_Identifier_Disease__c":[{"URL__c":"https://www.ncbi.nlm.nih.gov/medgen/?term=419414","Source__c":"C2931443","Xref__c":"MEDGEN:419414"},{"URL__c":"https://www.ncbi.nlm.nih.gov/mesh/C537222","Source__c":"MONDO:0042961","Xref__c":"C537222"},{"URL__c":"https://uts.nlm.nih.gov/uts/umls/concept/C2931443","Source__c":"C2931443","Xref__c":"C2931443"},{"URL__c":"http://purl.obolibrary.org/obo/MONDO_0042961","Source__c":"GARD:0000317","Xref__c":"MONDO:0042961"}],"Inheritance__c":["Autosomal dominant"],"tags":{},"synonyms":[""]}