{"Name":"Dianzani autoimmune lymphoproliferative disease","DiseaseID__c":"GARD:0009797","id":9797,"encodedName":"dianzani-autoimmune-lymphoproliferative-disease","IsDeleted":false,"Disease_Name_Full__c":"Dianzani autoimmune lymphoproliferative disease","Xref_IDs__c":"721093000; C2931071; C535950; MEDGEN:418980; MONDO:0011524; OMIM:605233; ORPHA:275523","USA_Estimate__c":"1,000","No_of_Specialist_Tagsa__c":4,"No_of_ClinGen_records__c":0,"No_of_GeneReviews__c":0,"No_of_HHS_records__c":0,"World_Estimate__c":"1 to 8,000","No_of_HRSA_records__c":0,"Evidence_Based_Score__c":0,"No_of_Disease_Descriptions__c":2,"Disease_Characteristics_Score__c":5,"No_of_Age_at_Onset__c":1,"Description_Source__c":"MONDO:0011524","Disease_Description__c":"Dianzani autoimmune lymphoproliferative disease (DALD) is a very rare disorder characterized by autoimmunity, lymphadenopathy and/or splenomegaly.","GARD_Name__c":"Dianzani autoimmune lymphoproliferative disease","GARD_Synonym__c":"autoimmune lymphoproliferative syndrome without fas mutations; dald; dald - dianzani autoimmune lymphoproliferative disease; dianzani autoimmune lymphoproliferative syndrome; dianzani form of autoimmune lymphoproliferative disease","Curated_Disease_Description_Source__c":"MONDO:0011524","Curated_Disease_Description__c":"Dianzani autoimmune lymphoproliferative disease (DALD) is a very rare disorder characterized by autoimmunity, lymphadenopathy and/or splenomegaly.","Curated_USA_Estimate_Source__c":null,"Curated_USA_Estimate__c":"1,000","Age_at_Onset_Snippet_Text__c":"at any time in life","SourceID__c":"ORPHA:275523","Deprecated__c":"No","Disease_Concept_Type__c":"Rare Disease Entity","MONDO_ID__c":"MONDO:0011524","ORPHANET_ID__c":"ORPHA:275523","Replaced_By_ID__c":null,"Display_Spanish_Disease_Name__c":"Enfermedad linfoproliferativa autoinmune de dianzani","Spanish_Description_Source__c":"ORPHA:275523","Spanish_Description__c":"La enfermedad linfoproliferativa autoinmune de Dianzani (DALD, siglas en inglés) es un trastorno muy poco frecuente que se caracteriza por autoinmunidad, linfadenopatía y/o esplenomegalia.","Spanish_Disease_Name__c":"enfermedad linfoproliferativa autoinmune de dianzani","Spanish_GARD_Synonym__c":"dald","Category_Linearization__c":"ORPHA:98004","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":"Dianzani autoimmune lymphoproliferative disease (DALD) is a very rare disorder characterized by autoimmunity, lymphadenopathy and/or splenomegaly.","Curated_Disease_Description_Source__c":"MONDO:0011524","GARD_Synonym__c":"autoimmune lymphoproliferative syndrome without fas mutations; dald; dald - dianzani autoimmune lymphoproliferative disease; dianzani autoimmune lymphoproliferative syndrome; dianzani form of autoimmune lymphoproliferative disease","Name":"Dianzani autoimmune lymphoproliferative disease","Curated_USA_Estimate__c":"1,000","estimateUsa":"1,000"}],"GARD_Disease_Tag__c":[{"Tag_Name__c":"Cancer - Oncologist","Tag_Category__c":"Specialist"},{"Tag_Name__c":"Genetics","Tag_Category__c":"Cause;Disease Category;Specialist","category_description":"Genetic diseases affect the DNA, or genetic instructions, which directs how tissues, organs, and body systems function.","curated_tag_name":"Genetic diseases"},{"Tag_Name__c":"Immunology","Tag_Category__c":"Specialist"},{"Tag_Name__c":"Primary Immune Deficiencies","Tag_Category__c":"Account","curated_tag_name":"Primary immunodeficiency"},{"Tag_Name__c":"Pediatrics","Tag_Category__c":"Specialist"}],"Age_At_Onset__c":[{"Age_At_Onset__c":"All ages","Provided_By__c":"ORPHA:275523"}],"External_Identifier_Disease__c":[{"URL__c":"https://www.ncbi.nlm.nih.gov/mesh/C535950","Source__c":"MONDO:0011524","Xref__c":"C535950"},{"URL__c":"https://browser.ihtsdotools.org/?perspective=full&conceptId1=721093000","Source__c":"C2931071; MONDO:0011524","Xref__c":"721093000"},{"URL__c":"https://www.ncbi.nlm.nih.gov/medgen/?term=418980","Source__c":"C2931071","Xref__c":"MEDGEN:418980"},{"URL__c":"https://uts.nlm.nih.gov/uts/umls/concept/C2931071","Source__c":"C2931071","Xref__c":"C2931071"},{"URL__c":"https://www.orpha.net/en/disease/detail/275523","Source__c":"C2931071; MONDO:0011524; ORPHA:275523","Xref__c":"ORPHA:275523"},{"URL__c":"https://www.omim.org/entry/605233","Source__c":"C2931071; MONDO:0011524; ORPHA:275523","Xref__c":"OMIM:605233"},{"URL__c":"http://purl.obolibrary.org/obo/MONDO_0011524","Source__c":"GARD:0009797","Xref__c":"MONDO:0011524"}],"tags":{"Specialist":["Cancer - Oncologist","Genetics","Immunology","Pediatrics"],"Cause":["Genetics"],"Disease Category":["Genetics"],"Account":["Primary Immune Deficiencies"]},"synonyms":["autoimmune lymphoproliferative syndrome without fas mutations"," dald"," dald - dianzani autoimmune lymphoproliferative disease"," dianzani autoimmune lymphoproliferative syndrome"," dianzani form of autoimmune lymphoproliferative disease"]}