Human Diseases

[ Brite menu | Download htext | Download json | Help ]
Search

1st Level  2nd Level  3rd Level 

 Cancers
 
 Immune system diseases
 
 Nervous system diseases
 
 Cardiovascular diseases
   Cardiac diseases
   Vascular diseases
     H01849  Peripheral arteriovenous malformation
     H00532  Parkes Weber syndrome [PATH:hsa04010]
     H00533  Hereditary hemorrhagic telangiectasia [PATH:hsa04350]
     H00534  Cerebral cavernous malformation
     H01482  Infantile hemangioma [PATH:hsa04370]
     H01875  Infantile hepatic hemangioma
     H00536  Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) [PATH:hsa04330]
     H00579  Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps (HANAC) [PATH:hsa04510 hsa04512]
     H01757  Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
     H00771  Inherited erythromelalgia
     H00800  Loeys-Dietz syndrome [PATH:hsa04010 hsa04060 hsa04144 hsa04350 hsa04380 hsa04390 hsa04520]
     H00801  Familial thoracic aortic aneurysm and dissection [PATH:hsa04270 hsa04010 hsa04020 hsa04060 hsa04350 hsa04510 hsa04520 hsa04530 hsa04810]
     H00877  Brain small vessel disease [PATH:hsa04510 hsa04512]
     H00896  Lymphangioleiomyomatosis [PATH:hsa04115 hsa04150 hsa04910]
     H01471  Lymphangioma
     H01735  Lymphangiomatosis
     H00919  Arterial tortuosity syndrome
     H00939  Darsun syndrome
     H01002  Generalized arterial calcification of infancy [PATH:hsa00230 hsa00500 hsa00740 hsa00760 hsa00770 hsa01100]
     H01006  Hereditary angioedema [PATH:hsa04610]
     H01120  Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome
     H01382  Polyarteritis nodosa
     H00824  Calcification of joints and arteries [PATH:hsa00230 hsa00240 hsa00760 hsa01100]
     H01396  Moyamoya disease [PATH:hsa04270]
     H01433  Budd-Chiari syndrome
     H01465  Large-vessel vasculitis
     H01698  Giant cell arteritis
     H01468  Eosinophilic granulomatosis with polyangiitis
     H01625  Buerger disease
     H01626  Arteriosclerosis obliterans
     H01629  Chronic arterial occlusive disease
     H01630  Patent ductus arteriosus [PATH:hsa04270]
     H01620  Raynaud syndrome
     H01658  Microscopic polyangiitis
     H01687  Extrahepatic portal vein obstruction
     H01723  Deep vein thrombosis
     H01718  Kawasaki disease
     H01742  Coronary artery disease [PATH:hsa04022 hsa04310]
     H01788  Klippel-Trenaunay-Weber syndrome
     H01809  Sturge-Weber syndrome
     H01866  Pulmonary veno-occlusive disease and pulmonary capillary hemangiomatosis
     H02088  Primary intraosseous vascular malformation
   Hematologic diseases
   Hypertensive diseases
 
 Respiratory diseases
 
 Endocrine and metabolic diseases
 
 Digestive system diseases
 
 Urinary system diseases
 
 Reproductive system diseases
 
 Musculoskeletal diseases
 
 Skin diseases
 
 Congenital disorders of metabolism
 
 Congenital malformations
 
 Other congenital disorders
 
 Other diseases

[ DISEASE | BRITE | KEGG2 | KEGG ]
Last updated: January 15, 2021

» Japanese version