{"Name":"Central polydactyly of fingers","DiseaseID__c":"GARD:0021200","id":21200,"encodedName":"central-polydactyly-of-fingers","IsDeleted":false,"Disease_Name_Full__c":"Central polydactyly of fingers","Xref_IDs__c":"205130008; C0431903; MEDGEN:609220; MONDO:0017456; ORPHA:295004","USA_Estimate__c":null,"No_of_Specialist_Tagsa__c":2,"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":2,"Disease_Characteristics_Score__c":3,"No_of_Age_at_Onset__c":0,"Description_Source__c":"ORPHA:295004","Disease_Description__c":"A rare congenital limb malformation characterized by complete or partial duplication of one of the three middle digits in a hand or foot. It most commonly affects the fourth digit. The malformation may be unilateral or bilateral and can occur as an isolated defect or in association with other anomalies.","GARD_Name__c":"Central polydactyly of fingers","GARD_Synonym__c":"central polydactyly; central polydactyly of hand; insertional polydactyly; intercalary polydactyly; mesoaxial polydactyly; mesoaxial polydactyly of fingers; mirror hand","Curated_Disease_Description_Source__c":"ORPHA:295004","Curated_Disease_Description__c":"A rare congenital limb malformation characterized by complete or partial duplication of one of the three middle digits in a hand or foot. It most commonly affects the fourth digit. The malformation may be unilateral or bilateral and can occur as an isolated defect or in association with other anomalies.","Curated_USA_Estimate_Source__c":null,"Curated_USA_Estimate__c":null,"Age_at_Onset_Snippet_Text__c":null,"SourceID__c":"ORPHA:295004","Deprecated__c":"No","Disease_Concept_Type__c":"Rare Disease Grouping","MONDO_ID__c":"MONDO:0017456","ORPHANET_ID__c":"ORPHA:295004","Replaced_By_ID__c":null,"Display_Spanish_Disease_Name__c":"Polidactilia central","Spanish_Description_Source__c":null,"Spanish_Description__c":null,"Spanish_Disease_Name__c":"polidactilia central","Spanish_GARD_Synonym__c":"polidactilia en espejo; polidactilia mesoaxial","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 congenital limb malformation characterized by complete or partial duplication of one of the three middle digits in a hand or foot. It most commonly affects the fourth digit. The malformation may be unilateral or bilateral and can occur as an isolated defect or in association with other anomalies.","Curated_Disease_Description_Source__c":"ORPHA:295004","GARD_Synonym__c":"central polydactyly; central polydactyly of hand; insertional polydactyly; intercalary polydactyly; mesoaxial polydactyly; mesoaxial polydactyly of fingers; mirror hand","Name":"Central polydactyly of fingers","estimateUsa":""}],"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":"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":"Orthopedics","Tag_Category__c":"Specialist"},{"Tag_Name__c":"Congenital limb malformation","Tag_Category__c":"Account","curated_tag_name":"Limb anomalies"}],"External_Identifier_Disease__c":[{"URL__c":"https://browser.ihtsdotools.org/?perspective=full&conceptId1=205130008","Source__c":"C0431903; MONDO:0017456","Xref__c":"205130008"},{"URL__c":"https://www.ncbi.nlm.nih.gov/medgen/?term=609220","Source__c":"C0431903","Xref__c":"MEDGEN:609220"},{"URL__c":"https://uts.nlm.nih.gov/uts/umls/concept/C0431903","Source__c":"C0431903","Xref__c":"C0431903"},{"URL__c":"https://www.orpha.net/en/disease/detail/295004","Source__c":"C0431903; MONDO:0017456; ORPHA:295004","Xref__c":"ORPHA:295004"},{"URL__c":"http://purl.obolibrary.org/obo/MONDO_0017456","Source__c":"GARD:0021200","Xref__c":"MONDO:0017456"},{"URL__c":"https://hpo.jax.org/browse/term/HP:0100260","Source__c":"C0431903","Xref__c":"HP:0100260"}],"tags":{"Cause":["Genetics"],"Disease Category":["Genetics","Congenital Abnormality"],"Specialist":["Genetics","Orthopedics"],"Account":["Congenital limb malformation"]},"synonyms":["central polydactyly"," central polydactyly of hand"," insertional polydactyly"," intercalary polydactyly"," mesoaxial polydactyly"," mesoaxial polydactyly of fingers"," mirror hand"]}