{"Name":"Accessory pancreas","DiseaseID__c":"GARD:0000454","id":454,"encodedName":"accessory-pancreas","IsDeleted":false,"Disease_Name_Full__c":"Accessory pancreas","Xref_IDs__c":"79037006; C0266268; C536003; MEDGEN:82737; MONDO:0019034; ORPHA:674","USA_Estimate__c":"1,000","No_of_Specialist_Tagsa__c":3,"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":4,"No_of_Age_at_Onset__c":2,"Description_Source__c":"MONDO:0019034","Disease_Description__c":"A rare asymptomatic embryopathy characterized by the presence of pancreatic tissue in other sites of the body such as the splenic pedicle, gonadic pedicles, intestinal mesentery, duodenum wall, upper jejunum, or, more rarely, the gastric wall, ileum, gallbladder or spleen.","GARD_Name__c":"Accessory pancreas","GARD_Synonym__c":"supernumerary pancreas","Curated_Disease_Description_Source__c":"MONDO:0019034","Curated_Disease_Description__c":"A rare asymptomatic embryopathy characterized by the presence of pancreatic tissue in other sites of the body such as the splenic pedicle, gonadic pedicles, intestinal mesentery, duodenum wall, upper jejunum, or, more rarely, the gastric wall, ileum, gallbladder or spleen.","Curated_USA_Estimate_Source__c":null,"Curated_USA_Estimate__c":"1,000","Age_at_Onset_Snippet_Text__c":"as a Newborn and as an Infant","SourceID__c":"ORPHA:674","Deprecated__c":"No","Disease_Concept_Type__c":"Rare Disease Entity","MONDO_ID__c":"MONDO:0019034","ORPHANET_ID__c":"ORPHA:674","Replaced_By_ID__c":null,"Display_Spanish_Disease_Name__c":"Páncreas accesorio","Spanish_Description_Source__c":"ORPHA:674","Spanish_Description__c":"Es una embriopatía asintomática caracterizada por la presencia de tejido pancreático en otros lugares del organismo, como el pedículo esplénico, los pedículos gonádicos, el mesenterio intestinal, la pared del duodeno, el yeyuno superior o, más raramente, la pared gástrica, el íleo, la vesícula biliar o el bazo.","Spanish_Disease_Name__c":"páncreas accesorio","Spanish_GARD_Synonym__c":null,"Category_Linearization__c":"ORPHA:93890","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":"A rare asymptomatic embryopathy characterized by the presence of pancreatic tissue in other sites of the body such as the splenic pedicle, gonadic pedicles, intestinal mesentery, duodenum wall, upper jejunum, or, more rarely, the gastric wall, ileum, gallbladder or spleen.","Curated_Disease_Description_Source__c":"MONDO:0019034","GARD_Synonym__c":"supernumerary pancreas","Name":"Accessory pancreas","Curated_USA_Estimate__c":"1,000","estimateUsa":"1,000"}],"GARD_Disease_Tag__c":[{"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":"Gastroenterology","Tag_Category__c":"Disease Category;Specialist","category_description":"Gastrointestinal diseases, or digestive diseases, affect the esophagus, stomach, small intestine, large intestine, liver, gallbladder, or pancreas.","curated_tag_name":"Gastrointestinal diseases"},{"Tag_Name__c":"Congenital Abnormality","Tag_Category__c":"Disease Category","category_description":"Birth defects are structural changes present at birth that can affect almost any part of the body, including how the body looks, works, or both.","curated_tag_name":"Birth defects"},{"Tag_Name__c":"Pediatrics","Tag_Category__c":"Specialist"}],"Age_At_Onset__c":[{"Age_At_Onset__c":"Infancy","Provided_By__c":"ORPHA:674"},{"Age_At_Onset__c":"Neonatal","Provided_By__c":"ORPHA:674"}],"External_Identifier_Disease__c":[{"URL__c":"https://www.ncbi.nlm.nih.gov/mesh/C536003","Source__c":"MONDO:0019034","Xref__c":"C536003"},{"URL__c":"https://www.orpha.net/en/disease/detail/674","Source__c":"C0266268; MONDO:0019034; ORPHA:674","Xref__c":"ORPHA:674"},{"URL__c":"https://browser.ihtsdotools.org/?perspective=full&conceptId1=79037006","Source__c":"C0266268; MONDO:0019034","Xref__c":"79037006"},{"URL__c":"https://uts.nlm.nih.gov/uts/umls/concept/C0266268","Source__c":"C0266268","Xref__c":"C0266268"},{"URL__c":"https://www.ncbi.nlm.nih.gov/medgen/?term=82737","Source__c":"C0266268","Xref__c":"MEDGEN:82737"},{"URL__c":"http://purl.obolibrary.org/obo/MONDO_0019034","Source__c":"GARD:0000454","Xref__c":"MONDO:0019034"}],"tags":{"Cause":["Genetics"],"Disease Category":["Genetics","Gastroenterology","Congenital Abnormality"],"Specialist":["Genetics","Gastroenterology","Pediatrics"]},"synonyms":["supernumerary pancreas"]}