Gangrene
Symptom Information:
Symptom ID: | HPO:0100758 | |||||||||||||||||||
Synonyms: |
|
|||||||||||||||||||
Quality: | ||||||||||||||||||||
Cross references: |
|
|||||||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Gangrene(HPO:0100758) MedDRA: Vascular disorders(MedDRA:10047065) Arteriosclerosis, stenosis, vascular insufficiency and necrosis(MedDRA:10003216) Musculoskeletal necrosis and vascular insufficiency(MedDRA:10065876) Gangrene(HPO:0100758) |
|||||||||||||||||||
Database Frequency: | 25 / 7739 | |||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Behçet disease | (Orphanet:117) |
Buerger disease | (Orphanet:36258) |
Cobb syndrome | (Orphanet:53721) |
Cryoglobulinemic vasculitis | (Orphanet:91138) |
Cutaneous leukocytoclastic angiitis | (Orphanet:889) |
Dermatomyositis | (Orphanet:221) |
Dracunculiasis | (Orphanet:231) |
Dystrophic epidermolysis bullosa | (Orphanet:303) |
Giant cell arteritis | (Orphanet:397) |
Granulomatosis with polyangiitis | (Orphanet:900) |
Hereditary thrombophilia due to congenital protein C deficiency | (Orphanet:745) |
Hereditary thrombophilia due to congenital protein S deficiency | (Orphanet:743) |
Ichthyosis hystrix of Curth-Macklin | (Orphanet:79503) |
Lamellar ichthyosis | (Orphanet:313) |
Microcephaly - lymphedema - chorioretinopathy | (Orphanet:2526) |
Microscopic polyangiitis | (Orphanet:727) |
Polyarteritis nodosa | (Orphanet:767) |
Primary hyperoxaluria | (Orphanet:416) |
Primary hyperoxaluria type 1 | (Orphanet:93598) |
Primary intestinal lymphangiectasia | (Orphanet:90362) |
Relapsing polychondritis | (Orphanet:728) |
Scleroderma | (Orphanet:801) |
Scrub typhus | (Orphanet:83317) |
Sézary syndrome | (Orphanet:3162) |
Takayasu arteritis | (Orphanet:3287) |