familial thoracic aortic aneurysm and aortic dissection +
fasciitis +
fulminant viral hepatitis
gastritis +
gastroenteritis +
glossitis +
gonococcal cervicitis +
Hemangiopericytic Neoplasm +
hepatic tuberculosis
hepatic vascular disorder +
Hepatitis, Alcoholic
Hepatopulmonary Syndrome
hereditary arterial and articular multiple calcification syndrome
hidradenitis +
inflammation of heart layer +
ischemic colitis
ischemic disease +
keratitis +
labyrinthitis +
laryngitis +
lethal arteriopathy syndrome due to fibulin-4 deficiency
Loeys-Dietz syndrome +
lymphadenitis +
lymphatic malformation +
lymphatic vessel neoplasm +
macrovascular complications of diabetes
mastitis
mediastinitis
multiple cutaneous and mucosal venous malformations
multisystemic smooth muscle dysfunction syndrome
myositis +
nasopharyngitis +
neonatal Marfan syndrome
nephritis +
neuritis +
neurovascular disorder +
non-alcoholic steatohepatitis
ocular vascular disease +
oophoritis +
oral tuberculosis
orchitis
Otitis media +
pancreatitis +
panniculitis +
parotitis
patent ductus arteriosus 2
PDA1
Pelvic Inflammatory Disease +
pericarditis +
perinephritis
periodontitis +
periostitis
peripheral vascular disease +
pharyngitis +
pneumonitis +
posthitis +
proctitis +
prostatitis +
pulmonary venoocclusive disease +
pulpitis
pyometritis +
radiculitis
renal nutcracker syndrome
rheumatic heart disease +
rhinitis +
serositis +
sinusitis +
skin vascular disease +
small artery occlusion
spondylitis +
STING-associated vasculopathy with onset in infancy
stomatitis +
Superior Vena Cava Syndrome
Systemic capillary leak syndrome
thoracic outlet syndrome +
thromboangiitis obliterans
thrombotic disease +
thyroiditis +
tonsillitis +
tracheobronchitis +
urethritis +
uveitis +
vaginitis +
vascular anomaly +
vascular disorder of penis
vascular ectasia +
vascular hemostatic disease +
vascular insufficiency disorder +
vascular malformation +
vascular occlusion disorder +
vascular toxicity
vasculitis +
A group of disorders that destroy blood vessels by inflammation. Both arteries and veins are affected. Vasculitis represents a clinically heterogenous group of diseases of multifactorial etiology characterized by inflammation of either large-sized vessels (large-vessel vasculitis, e.g. Giant-cell arteritis and Takayasu arteritis), medium-sized vessels (medium-vessel vasculitis e.g. polyarteritis nodosa and Kawasaki disease), or small-sized vessels (small-vessel vasculitis, e.g. granulomatosis with polyangiitis, microscopic polyangiitis, immunoglobulin A vasculitis, and cutaneous leukocytoclastic angiitis). Vasculitis occurs at any age, may be acute or chronic, and manifests with general symptoms such as fever, weight loss and fatigue, as well as more specific clinical signs depending on the type of vessels and organs affected. The degree of severity is variable, ranging from life or sight threatening disease (e.g. Behcet disease) to relatively minor skin disease.