{"Name":"Familial partial epilepsy","DiseaseID__c":"GARD:0002173","id":2173,"encodedName":"familial-partial-epilepsy","IsDeleted":false,"Disease_Name_Full__c":"Familial partial epilepsy","Xref_IDs__c":"C5680862; MEDGEN:1826100; MONDO:0017704; ORPHA:309","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":1,"Disease_Characteristics_Score__c":5,"No_of_Age_at_Onset__c":0,"Description_Source__c":"MONDO:0017704","Disease_Description__c":"An instance of partial epilepsy that is caused by an inherited modification of the individual's genome.","GARD_Name__c":"Familial partial epilepsy","GARD_Synonym__c":"familial focal epilepsy; hereditary partial epilepsy","Curated_Disease_Description_Source__c":"MONDO:0017704","Curated_Disease_Description__c":"An instance of partial epilepsy that is caused by an inherited modification of the individual's genome.","Curated_USA_Estimate_Source__c":null,"Curated_USA_Estimate__c":null,"Age_at_Onset_Snippet_Text__c":null,"SourceID__c":"ORPHA:309","Deprecated__c":"No","Disease_Concept_Type__c":"Rare Disease Grouping","MONDO_ID__c":"MONDO:0017704","ORPHANET_ID__c":"ORPHA:309","Replaced_By_ID__c":null,"Display_Spanish_Disease_Name__c":"Epilepsia parcial familiar","Spanish_Description_Source__c":null,"Spanish_Description__c":null,"Spanish_Disease_Name__c":"epilepsia parcial familiar","Spanish_GARD_Synonym__c":null,"Category_Linearization__c":"ORPHA:98006","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":"An instance of partial epilepsy that is caused by an inherited modification of the individual's genome.","Curated_Disease_Description_Source__c":"MONDO:0017704","GARD_Synonym__c":"familial focal epilepsy; hereditary partial epilepsy","Name":"Familial partial epilepsy","estimateUsa":""}],"Organization_Supported_Diseases__c":[{"Account_Name__c":"Epilepsy Foundation","Website__c":"https://www.epilepsy.com/"}],"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":"Neurology","Tag_Category__c":"Disease Category;Specialist","category_description":"Neurological diseases affect the brain, spinal cord, cranial nerves, autonomic nerves, or other peripheral nerves.","curated_tag_name":"Neurological diseases"},{"Tag_Name__c":"Epilepsy","Tag_Category__c":"Account;Specialist","curated_tag_name":"Epilepsy"}],"External_Identifier_Disease__c":[{"URL__c":"https://www.orpha.net/en/disease/detail/309","Source__c":"C5680862; MONDO:0017704; ORPHA:309","Xref__c":"ORPHA:309"},{"URL__c":"https://uts.nlm.nih.gov/uts/umls/concept/C5680862","Source__c":"C5680862","Xref__c":"C5680862"},{"URL__c":"https://www.ncbi.nlm.nih.gov/medgen/?term=1826100","Source__c":"C5680862","Xref__c":"MEDGEN:1826100"},{"URL__c":"http://purl.obolibrary.org/obo/MONDO_0017704","Source__c":"GARD:0002173","Xref__c":"MONDO:0017704"}],"tags":{"Cause":["Genetics"],"Disease Category":["Genetics","Neurology"],"Specialist":["Genetics","Neurology","Epilepsy"],"Account":["Epilepsy"]},"synonyms":["familial focal epilepsy"," hereditary partial epilepsy"]}