{"Name":"Familial cervical artery dissection","DiseaseID__c":"GARD:0018823","id":18823,"encodedName":"familial-cervical-artery-dissection","IsDeleted":false,"Disease_Name_Full__c":"Familial cervical artery dissection","Xref_IDs__c":"C4755308; MEDGEN:1659372; MONDO:0018212","USA_Estimate__c":null,"No_of_Specialist_Tagsa__c":1,"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":2,"No_of_Age_at_Onset__c":0,"Description_Source__c":"MONDO:0018212","Disease_Description__c":"An instance of cervical artery dissection that is caused by an inherited modification of the individual's genome.","GARD_Name__c":"Familial cervical artery dissection","GARD_Synonym__c":"familial cad; hereditary cad; hereditary cervical artery dissection","Curated_Disease_Description_Source__c":"ORPHA:36382","Curated_Disease_Description__c":"Familial cervical artery dissection is a rare, genetic, neurological disorder characterized by dissection of the cervical artery in various members of a single family, presenting with variable manifestations which range from asymptomatic to the triad of ipsilateral pain in the head, neck, and face, Horner syndrome, and cerebral or retinal ischemic symptoms. Headache and cerebral ischemic features are most frequently observed.","Curated_USA_Estimate_Source__c":null,"Curated_USA_Estimate__c":null,"Age_at_Onset_Snippet_Text__c":null,"SourceID__c":"ORPHA:36382","Deprecated__c":"No","Disease_Concept_Type__c":"Rare Disease Entity","MONDO_ID__c":"MONDO:0018212","ORPHANET_ID__c":null,"Replaced_By_ID__c":null,"Display_Spanish_Disease_Name__c":null,"Spanish_Description_Source__c":null,"Spanish_Description__c":null,"Spanish_Disease_Name__c":null,"Spanish_GARD_Synonym__c":null,"Category_Linearization__c":null,"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":"Familial cervical artery dissection is a rare, genetic, neurological disorder characterized by dissection of the cervical artery in various members of a single family, presenting with variable manifestations which range from asymptomatic to the triad of ipsilateral pain in the head, neck, and face, Horner syndrome, and cerebral or retinal ischemic symptoms. Headache and cerebral ischemic features are most frequently observed.","Curated_Disease_Description_Source__c":"ORPHA:36382","GARD_Synonym__c":"familial cad; hereditary cad; hereditary cervical artery dissection","Name":"Familial cervical artery dissection","estimateUsa":""}],"Organization_Supported_Diseases__c":[{"Account_Name__c":"American Heart Association","Website__c":"https://www.heart.org"}],"GARD_Disease_Tag__c":[{"Tag_Name__c":"Vascular Medicine","Tag_Category__c":"Specialist","curated_tag_name":"Vascular diseases"}],"External_Identifier_Disease__c":[{"URL__c":"https://www.ncbi.nlm.nih.gov/medgen/?term=1659372","Source__c":"C4755308","Xref__c":"MEDGEN:1659372"},{"URL__c":"https://uts.nlm.nih.gov/uts/umls/concept/C4755308","Source__c":"C4755308","Xref__c":"C4755308"},{"URL__c":"http://purl.obolibrary.org/obo/MONDO_0018212","Source__c":"GARD:0018823","Xref__c":"MONDO:0018212"}],"tags":{"Specialist":["Vascular Medicine"]},"synonyms":["familial cad"," hereditary cad"," hereditary cervical artery dissection"]}