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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
AIDS Arteritis, Central Nervous System 
angioedema +   
angioma serpiginosum +  
antiphospholipid syndrome +   
autoimmune atherosclerosis 
autoimmune cardiomyopathy 
autoimmune epilepsy 
autoimmune myocarditis +   
autoimmune neuropathy 
autoimmune vasculitis 
bacillary angiomatosis 
Behcet's disease  
cerebral arteritis 
Cutis Marmorata Telangiectatica Congenita 
Demyelinating Autoimmune Diseases, CNS +   
Endarteritis 
Familial Granulomatous Arteritis with Juvenile Polyarthritis 
Gardner-Diamond Syndrome 
granulomatous angiitis 
Kawasaki disease  
Libman-Sacks endocarditis 
limbic encephalitis 
Livedo Reticularis +   
livedoid vasculitis 
Lupus Vasculitis, Central Nervous System  
Malignant Atrophic Papulosis 
Megalencephaly - Cutis Marmorata Telangiectatica Congenita  
polyarteritis nodosa +   
postinfectious encephalitis 
Primary Angiitis of the Central Nervous System 
pyoderma gangrenosum +   
rheumatic pulmonary valve disease 
Sneddon syndrome  
STING-associated vasculopathy with onset in infancy  
Takayasu's arteritis  
temporal arteritis  
A central nervous system vasculitis that is characterized by inflammation of the lining of arteries, often arteries in the head. (DO)
urticaria +   

Synonyms
Exact Synonyms: Giant Cell Aortitis ;   Giant Cell Aortitis, Horton's ;   Giant Cell Arteritis ;   Horton Disease ;   Horton Giant Cell Arteritis ;   Horton's Disease ;   Horton's Giant Cell Arteritis ;   Hortons Disease ;   Juvenile cranial arteritis ;   cranial arteritides
Primary IDs: MESH:D013700
Alternate IDs: MESH:C538533 ;   MIM:187360
Xrefs: EFO:1001209 ;   ICD9CM:446.5 ;   NCI:C35065 ;   ORDO:397
Definition Sources: https://www.mayoclinic.org/diseases-conditions/giant-cell-arteritis/symptoms-causes/syc-20372758 "DO" "DO"

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