Arterial stenosis
Symptom Information:
Symptom ID: | HPO:0100545 | ||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) 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) MedDRA: 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) |
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Database Frequency: | 22 / 7739 | ||||||||
Resource: |
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) |