Venous insufficiency

Symptom Information:

Symptom ID: HPO:0005293
Peripheral venous insufficiency (disorder) [Orphanet:35660]
Venous Insufficiency [Orphanet:35660]
Varices/varicous veins/venous insufficiency [Orphanet:35660]
Venous insufficiency [Orphanet:35660]
Venous insufficiency [MedDRA:10057320]
Venostasis [MedDRA:10057320]
Venous (peripheral) insufficiency, unspecified [MedDRA:10057320]
Venous stasis [MedDRA:10057320]
Venous oedema [MedDRA:10057320]
Venous edema [MedDRA:10057320]
Chronic venous insufficiency [MedDRA:10057320]
Hypostasis [MedDRA:10057320]
Venous reflux [MedDRA:10057320]
Venous valvular incompetency [MedDRA:10057320]
Cross references:
Orphanet:35660 "Varices/varicous veins/venous insufficiency" [Orphanet:35660]
UMLS:C0042485 "Venous Insufficiency" [Orphanet:35660]
Is a (Direct Parents):
Orphanet Varicose veins
HPO         Venous abnormality
MedDRA Non-site specific necrosis and vascular insufficiency NEC
Orphanet Abnormality of cardiovascular system physiology
Is a (Whole tree): HPO:
    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)
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)
Database Frequency: 27 / 7739

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)