Gangrene

Symptom Information:

Symptom ID: HPO:0100758
Synonyms:
Gangrenous disorder (disorder) [Orphanet:35810]
Gangrene (morphologic abnormality) [Orphanet:35810]
Gangrene [Orphanet:35810]
Gangrene [OMIM:Gangrene]
Gangrena/necrosis [Orphanet:35810]
Gangrene [MedDRA:10017711]
Gangrene cutaneous [MedDRA:10017711]
Gangrene hemorrhagic [MedDRA:10017711]
Gangrene NOS [MedDRA:10017711]
Gangrene peripheral [MedDRA:10017711]
Gangrene presenile [MedDRA:10017711]
Gangrene skin [MedDRA:10017711]
Gangrene spontaneous [MedDRA:10017711]
Gangrene static [MedDRA:10017711]
Gangrene symmetrical [MedDRA:10017711]
Peripheral gangrene [MedDRA:10017711]
Gangrene toe [MedDRA:10017711]
Gangrene haemorrhagic [MedDRA:10017711]
Wet gangrene [MedDRA:10017711]
Quality:
Cross references:
Orphanet:35810 "Gangrena/necrosis" [Orphanet:35810]
OMIM: "Gangrene" [OMIM:Gangrene]
UMLS:C0017086 "Gangrene" [HPO:0100758]
UMLS:C0017086 "Gangrene" [Orphanet:35810]
Is a (Direct Parents):
Orphanet Acute ischemic syndrome
HPO         Abnormality of metabolism/homeostasis
MedDRA Musculoskeletal necrosis and vascular insufficiency
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)