{"Name":"True unicornuate uterus","DiseaseID__c":"GARD:0020174","id":20174,"encodedName":"true-unicornuate-uterus","IsDeleted":false,"Disease_Name_Full__c":"True unicornuate uterus","Xref_IDs__c":"C5848180; MEDGEN:1863468; MONDO:0015832; ORPHA:180074","USA_Estimate__c":null,"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":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":"MONDO:0015832","Disease_Description__c":"A rare, non-syndromic uterovaginal malformation characterized by a crescent-shaped, small-sized uterus containing a single horn and fallopian tube with no rudimentary horn. Urinary tract anomalies are frequently associated.","GARD_Name__c":"True unicornuate uterus","GARD_Synonym__c":"complete unilateral aplasia of the mullerian ducts; complete unilateral aplasia of the müllerian ducts; complete unilateral mullerian aplasia; complete unilateral müllerian aplasia; unicornuate uterus without rudimentary horn","Curated_Disease_Description_Source__c":"MONDO:0015832","Curated_Disease_Description__c":"A rare, non-syndromic uterovaginal malformation characterized by a crescent-shaped, small-sized uterus containing a single horn and fallopian tube with no rudimentary horn. Urinary tract anomalies are frequently associated.","Curated_USA_Estimate_Source__c":null,"Curated_USA_Estimate__c":null,"Age_at_Onset_Snippet_Text__c":null,"SourceID__c":"ORPHA:180074","Deprecated__c":"No","Disease_Concept_Type__c":"Rare Disease Entity","MONDO_ID__c":"MONDO:0015832","ORPHANET_ID__c":"ORPHA:180074","Replaced_By_ID__c":null,"Display_Spanish_Disease_Name__c":"Útero unicorne verdadero","Spanish_Description_Source__c":"ORPHA:180074","Spanish_Description__c":"Es una malformación uterovaginal no sindrómica poco frecuente caracterizada por un útero de tamaño pequeño y en forma de media luna con un solo cuerno y trompa de Falopio, sin cuerno rudimentario. Se asocian con frecuencia anomalías en el tracto urinario.","Spanish_Disease_Name__c":"útero unicorne verdadero","Spanish_GARD_Synonym__c":"aplasia mulleriana unilateral completa; aplasia unilateral completa de los conductos de müller; útero unicorne sin cuerno rudimentario","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, non-syndromic uterovaginal malformation characterized by a crescent-shaped, small-sized uterus containing a single horn and fallopian tube with no rudimentary horn. Urinary tract anomalies are frequently associated.","Curated_Disease_Description_Source__c":"MONDO:0015832","GARD_Synonym__c":"complete unilateral aplasia of the mullerian ducts; complete unilateral aplasia of the müllerian ducts; complete unilateral mullerian aplasia; complete unilateral müllerian aplasia; unicornuate uterus without rudimentary horn","Name":"True unicornuate uterus","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":"Urogenital Disorders","Tag_Category__c":"Disease Category","category_description":"Urinary and reproductive diseases affect the kidneys, ureters, bladder, urethra, or the reproductive organs.","curated_tag_name":"Urinary and reproductive diseases"},{"Tag_Name__c":"Obstetrics / Gynecology","Tag_Category__c":"Specialist"},{"Tag_Name__c":"Urologist","Tag_Category__c":"Specialist"}],"External_Identifier_Disease__c":[{"URL__c":"https://www.orpha.net/en/disease/detail/180074","Source__c":"C5848180; MONDO:0015832; ORPHA:180074","Xref__c":"ORPHA:180074"},{"URL__c":"https://www.ncbi.nlm.nih.gov/medgen/?term=1863468","Source__c":"C5848180","Xref__c":"MEDGEN:1863468"},{"URL__c":"http://purl.obolibrary.org/obo/MONDO_0015832","Source__c":"GARD:0020174","Xref__c":"MONDO:0015832"},{"URL__c":"https://uts.nlm.nih.gov/uts/umls/concept/C5848180","Source__c":"C5848180","Xref__c":"C5848180"}],"tags":{"Cause":["Genetics"],"Disease Category":["Genetics","Congenital Abnormality","Urogenital Disorders"],"Specialist":["Genetics","Obstetrics / Gynecology","Urologist"]},"synonyms":["complete unilateral aplasia of the mullerian ducts"," complete unilateral aplasia of the müllerian ducts"," complete unilateral mullerian aplasia"," complete unilateral müllerian aplasia"," unicornuate uterus without rudimentary horn"]}