Venous insufficiency
Symptom Information:
Symptom ID: | HPO:0005293 | ||||||||||||||
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) Venous abnormality(HPO:0002624) Venous insufficiency(HPO:0005293) MedDRA: Vascular disorders(MedDRA:10047065) Arteriosclerosis, stenosis, vascular insufficiency and necrosis(MedDRA:10003216) Non-site specific necrosis and vascular insufficiency NEC(MedDRA:10029558) Venous insufficiency(HPO:0005293) |
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Database Frequency: | 27 / 7739 | ||||||||||||||
Resource: |
All diseases associated with this symptom:
22q11.2 deletion syndrome | (Orphanet:567) |
Angio-osteohypertrophic syndrome | (Orphanet:2346) |
CADASIL | (Orphanet:136) |
Cardiomyopathy, familial restrictive 2 | (OMIM:609578) |
Ehlers-Danlos syndrome type 1 | (Orphanet:90309) |
Ehlers-Danlos syndrome type 2 | (Orphanet:90318) |
Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Familial multiple nevi flammei | (Orphanet:624) |
Hereditary thrombophilia due to congenital protein C deficiency | (Orphanet:745) |
Hereditary thrombophilia due to congenital protein S deficiency | (Orphanet:743) |
Hypotrichosis - lymphedema - telangiectasia | (Orphanet:69735) |
Klippel-Trénaunay syndrome | (Orphanet:90308) |
Lymphedema - distichiasis | (Orphanet:33001) |
Menkes disease | (Orphanet:565) |
Microphthalmia with limb anomalies | (Orphanet:1106) |
Norrie disease | (Orphanet:649) |
Occipital horn syndrome | (Orphanet:198) |
Parkes Weber syndrome | (Orphanet:90307) |
Proteus-like syndrome | (Orphanet:2969) |
Secondary polycythemia | (Orphanet:98428) |
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus | (Orphanet:137608) |
Thoracic outlet syndrome | (Orphanet:97330) |
Torticollis - keloids - cryptorchidism - renal dysplasia | (Orphanet:3341) |
Von Willebrand disease | (Orphanet:903) |
X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome | (Orphanet:324410) |