Arterial stenosis

Symptom Information:

Symptom ID: HPO:0100545
Stricture of artery (disorder) [Orphanet:35360]
Stricture of artery [Orphanet:35360]
Arterial stenosis [OMIM:Arterial stenosis]
Arterial stenosis/occlusion [Orphanet:35360]
Arterial stenosis [Orphanet:35360]
Arterial stenosis [MedDRA:10060965]
Arterial stenosis NOS [MedDRA:10060965]
Stricture of artery [MedDRA:10060965]
Cross references:
Orphanet:35360 "Arterial stenosis/occlusion" [Orphanet:35360]
OMIM: "Arterial stenosis" [OMIM:Arterial stenosis]
UMLS:C0038449 "Stricture of artery" [Orphanet:35360]
Is a (Direct Parents):
Orphanet Abnormality of cardiovascular system physiology
HPO         Abnormalities of the peripheral arteries
MedDRA Non-site specific necrosis and vascular insufficiency NEC
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of the vasculature(HPO:0002597)
             Abnormality of the systemic arterial tree(HPO:0011004)
                Abnormalities of the peripheral arteries(HPO:0005114)
                   Arterial stenosis(HPO:0100545)
Vascular disorders(MedDRA:10047065)
    Arteriosclerosis, stenosis, vascular insufficiency and necrosis(MedDRA:10003216)
       Non-site specific necrosis and vascular insufficiency NEC(MedDRA:10029558)
          Arterial stenosis(HPO:0100545)
Database Frequency: 22 / 7739

All diseases associated with this symptom:

Arterial calcification, generalized, of infancy, 1 (OMIM:208000)
Arterial tortuosity syndrome (Orphanet:3342)
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy (Orphanet:1192)
Autosomal recessive cutis laxa type 1 (Orphanet:90349)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
Cutis marmorata telangiectatica congenita (Orphanet:1556)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Grange syndrome (Orphanet:79094)
Hereditary arterial and articular multiple calcification syndrome (Orphanet:289601)
Hughes-Stovin syndrome (Orphanet:228116)
Menkes disease (Orphanet:565)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism (Orphanet:280679)
Neurofibromatosis type 1 (Orphanet:636)
PHACE syndrome (Orphanet:42775)
Polyarteritis nodosa (Orphanet:767)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Pseudoxanthoma elasticum (Orphanet:758)
Sneddon syndrome (Orphanet:820)
Systemic sclerosis (Orphanet:90291)
Takayasu arteritis (Orphanet:3287)
Williams syndrome (Orphanet:904)