Skin ulcer

Symptom Information:

Symptom ID: HPO:0200042
Sore on skin (disorder) [Orphanet:23190]
Skin ulcer (disorder) [Orphanet:23190]
Skin Ulcer [Orphanet:23190]
Chronic skin infection/ulcerations/ulcers/cancrum [Orphanet:23190]
Skin ulcer [Orphanet:23190]
Skin ulcer [MedDRA:10040943]
Chronic skin ulcer [MedDRA:10040943]
Chronic skin ulcer of other specified sites [MedDRA:10040943]
Chronic skin ulcer of unspecified site [MedDRA:10040943]
Chronic ulcer of other specified sites [MedDRA:10040943]
Chronic ulcer of skin [MedDRA:10040943]
Chronic ulcer of skin, other specified sites [MedDRA:10040943]
Chronic ulcer of skin, unspecified site [MedDRA:10040943]
Chronic ulcer of unspecified site [MedDRA:10040943]
Foot ulcer [MedDRA:10040943]
Ischaemic leg ulcer [MedDRA:10040943]
Leg ulcer (exc varicose) [MedDRA:10040943]
Lower extremities ulcers of [MedDRA:10040943]
Skin ulcer NOS [MedDRA:10040943]
Skin ulceration [MedDRA:10040943]
Stasis ulcer [MedDRA:10040943]
Ulcer foot [MedDRA:10040943]
Ulcer of lower limbs, except decubitus ulcer [MedDRA:10040943]
Ulcer skin [MedDRA:10040943]
Ulcers of extremities [MedDRA:10040943]
Venous stasis ulcer [MedDRA:10040943]
Venous ulcer NOS [MedDRA:10040943]
Venous ulceration [MedDRA:10040943]
Ankle ulcer [MedDRA:10040943]
Heel ulcer [MedDRA:10040943]
Skin sores [MedDRA:10040943]
Leg ulcer (excl varicose) [MedDRA:10040943]
Venous ulcer discharge [MedDRA:10040943]
Ischemic leg ulcer [MedDRA:10040943]
Ulcer of lower limbs, excl decubitus ulcer [MedDRA:10040943]
Venous ulcer odor [MedDRA:10040943]
Venous ulcer odour [MedDRA:10040943]
Skin trophic ulcer [MedDRA:10040943]
Ulcus cruris [MedDRA:10040943]
Chronic leg ulcer [MedDRA:10040943]
Venous ulcer recurrent [MedDRA:10040943]
Multiple skin ulcers [MedDRA:10040943]
Leg ulcer [MedDRA:10040943]
Digital ulcer [MedDRA:10040943]
Ulcer of upper extremity [MedDRA:10040943]
Digital ulcers [OMIM:Digital ulcers]
Leg ulcers [OMIM:Leg ulcers]
Skin ulceration [OMIM:Skin ulceration]
Skin ulcers [OMIM:Skin ulcers]
Venous stasis ulcer [OMIM:Venous stasis ulcer]
Cross references:
Orphanet:23190 "Chronic skin infection/ulcerations/ulcers/cancrum" [Orphanet:23190]
OMIM: "Digital ulcers" [OMIM:Digital ulcers]
OMIM: "Leg ulcers" [OMIM:Leg ulcers]
OMIM: "Skin ulceration" [OMIM:Skin ulceration]
OMIM: "Skin ulcers" [OMIM:Skin ulcers]
OMIM: "Venous stasis ulcer" [OMIM:Venous stasis ulcer]
UMLS:C0037299 "Skin Ulcer" [Orphanet:23190]
Is a (Direct Parents):
HPO         Localized skin lesion
Orphanet Abnormality of the skin
MedDRA Skin and subcutaneous tissue ulcerations
Orphanet Recurrent skin infections
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Localized skin lesion(HPO:0011355)
                Skin ulcer(HPO:0200042)
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Skin and subcutaneous tissue disorders NEC(MedDRA:10040790)
       Skin and subcutaneous tissue ulcerations(MedDRA:10040796)
          Skin ulcer(HPO:0200042)
Database Frequency: 138 / 7739

All diseases associated with this symptom:

ADULT syndrome (Orphanet:978)
Acquired ichthyosis (Orphanet:454)
Acrodermatitis enteropathica, zinc deficiency type (Orphanet:37)
Acrogeria (Orphanet:2500)
Acroosteolysis, dominant type (Orphanet:955)
Adiposis dolorosa (Orphanet:36397)
Adult polyglucosan body disease (Orphanet:206583)
Angio-osteohypertrophic syndrome (Orphanet:2346)
Aplasia cutis - myopia (Orphanet:1117)
Attenuated Chédiak-Higashi syndrome (Orphanet:352723)
Autosomal agammaglobulinemia (Orphanet:33110)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
Beta-thalassemia (Orphanet:848)
Beta-thalassemia intermedia (Orphanet:231222)
Beta-thalassemia major (Orphanet:231214)
Biotinidase deficiency (Orphanet:79241)
Blau syndrome (Orphanet:90340)
Buerger disease (Orphanet:36258)
Bullous impetigo (Orphanet:36237)
CREST syndrome (Orphanet:90290)
Cervical hypertrichosis - peripheral neuropathy (Orphanet:2218)
Chilblain lupus (Orphanet:90280)
Chronic granulomatous disease (Orphanet:379)
Chronic mucocutaneous candidiasis (Orphanet:1334)
Chédiak-Higashi syndrome (Orphanet:167)
Circumscribed cutaneous aplasia of the vertex (Orphanet:1114)
Classical mycosis fungoides (Orphanet:2584)
Cogan syndrome (Orphanet:1467)
Combined immunodeficiency due to DOCK8 deficiency (Orphanet:217390)
Cryoglobulinemic vasculitis (Orphanet:91138)
Cushing disease (Orphanet:96253)
Cutaneous leukocytoclastic angiitis (Orphanet:889)
Cutaneous lupus erythematosus (Orphanet:535)
Cutis marmorata telangiectatica congenita (Orphanet:1556)
Cyclic neutropenia (Orphanet:2686)
Dermatofibrosarcoma protuberans (Orphanet:31112)
Dermatomyositis (Orphanet:221)
Dermatoosteolysis, Kirghizian type (Orphanet:1657)
Diffuse cutaneous systemic sclerosis (Orphanet:220393)
Dissecting cellulitis of the scalp (Orphanet:345)
Dracunculiasis (Orphanet:231)
Dyskeratosis congenita (Orphanet:1775)
Dystrophic epidermolysis bullosa (Orphanet:303)
Ectodermal dysplasia - blindness (Orphanet:1806)
Ectodermal dysplasia syndrome (Orphanet:79373)
Enchondromatosis (Orphanet:296)
Epidermodysplasia verruciformis (Orphanet:302)
Epidermolysis bullosa simplex (Orphanet:304)
Epidermolysis bullosa simplex due to plakophilin deficiency (Orphanet:158668)
Epidermolysis bullosa simplex superficialis (Orphanet:89839)
Epidermolysis bullosa simplex, Dowling-Meara type (Orphanet:79396)
Epidermolytic ichthyosis (Orphanet:312)
Erosive pustular dermatosis of the scalp (Orphanet:222)
Familial benign chronic pemphigus (Orphanet:2841)
Familial keratoacanthoma (Orphanet:493)
Familial multiple nevi flammei (Orphanet:624)
Felty syndrome (Orphanet:47612)
Flynn-Aird syndrome (Orphanet:2047)
Free sialic acid storage disease (Orphanet:834)
Giant cell arteritis (Orphanet:397)
Good syndrome (Orphanet:169105)
Gorlin syndrome (Orphanet:377)
Granulomatosis with polyangiitis (Orphanet:900)
Haim-Munk syndrome (Orphanet:2342)
Hereditary acrokeratotic poikiloderma, Weary type (Orphanet:2907)
Hereditary sensory and autonomic neuropathy type 4 (Orphanet:642)
Hereditary sensory and autonomic neuropathy with spastic paraplegia (Orphanet:139578)
Hereditary thrombophilia due to congenital protein C deficiency (Orphanet:745)
Hereditary thrombophilia due to congenital protein S deficiency (Orphanet:743)
Hidrotic ectodermal dysplasia (Orphanet:189)
Hyperkeratosis lenticularis perstans (Orphanet:409)
Ichthyosis hystrix of Curth-Macklin (Orphanet:79503)
Immunodeficiency by defective expression of HLA class 1 (Orphanet:34592)
Immunoglobulin A vasculitis (Orphanet:761)
Incontinentia pigmenti (Orphanet:464)
Infantile myofibromatosis (Orphanet:2591)
Inherited epidermolysis bullosa (Orphanet:79361)
Intestinal lymphangiectasia (Orphanet:36204)
Isolated agammaglobulinemia (Orphanet:229717)
Junctional epidermolysis bullosa (Orphanet:305)
Junctional epidermolysis bullosa - pyloric atresia (Orphanet:79403)
Junctional epidermolysis bullosa, Herlitz type (Orphanet:79404)
Junctional epidermolysis bullosa, non-Herlitz type (Orphanet:89840)
Juvenile dermatomyositis (Orphanet:93672)
Juvenile hyaline fibromatosis (Orphanet:2028)
KID syndrome (Orphanet:477)
Kerion celsi (Orphanet:499)
Kindler syndrome (Orphanet:2908)
LOC syndrome (Orphanet:2407)
Lethal acantholytic epidermolysis bullosa (Orphanet:158687)
Lichen planopilaris (Orphanet:525)
Limited cutaneous systemic sclerosis (Orphanet:220402)
Limited systemic sclerosis (Orphanet:220407)
Lipedema (Orphanet:77243)
Lyell syndrome (Orphanet:537)
Lymphedema - distichiasis (Orphanet:33001)
Mal de Meleda (Orphanet:87503)
Malakoplakia (Orphanet:556)
Microcephaly - lymphedema - chorioretinopathy (Orphanet:2526)
Microscopic polyangiitis (Orphanet:727)
Mutilating palmoplantar keratoderma with periorificial keratotic plaques (Orphanet:659)
Non-epidermolytic palmoplantar keratoderma (Orphanet:2337)
Oculocerebrorenal syndrome (Orphanet:534)
Oral erosive lichen (Orphanet:31142)
Palmoplantar keratoderma, Nagashima type (Orphanet:140966)
Papillon-Lefèvre syndrome (Orphanet:678)
Polyarteritis nodosa (Orphanet:767)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Primary cutaneous anaplastic large cell lymphoma (Orphanet:300865)
Primary cutaneous lymphoma (Orphanet:542)
Prolidase deficiency (Orphanet:742)
Proliferating trichilemmal cyst (Orphanet:492)
Pseudo-pelade of Brocq (Orphanet:129)
Pyoderma gangrenosum (Orphanet:48104)
Pyogenic arthritis - pyoderma gangrenosum - acne (Orphanet:69126)
Pyogenic bacterial infections due to MyD88 deficiency (Orphanet:183713)
Quinquaud's folliculitis decalvans (Orphanet:346)
Recessive aplasia cutis congenita of limbs (Orphanet:1115)
Recessive dystrophic epidermolysis bullosa inversa (Orphanet:79409)
Relapsing polychondritis (Orphanet:728)
Reticular dysgenesis (Orphanet:33355)
Reynolds syndrome (Orphanet:779)
Rothmund-Thomson syndrome (Orphanet:2909)
SAPHO syndrome (Orphanet:793)
Scleroderma (Orphanet:801)
Scrub typhus (Orphanet:83317)
Secondary intestinal lymphangiectasia (Orphanet:90363)
Sweet syndrome (Orphanet:3243)
Systemic sclerosis (Orphanet:90291)
Takayasu arteritis (Orphanet:3287)
Werner syndrome (Orphanet:902)
Wiskott-Aldrich syndrome (Orphanet:906)
Wrinkly skin syndrome (Orphanet:2834)
X-linked agammaglobulinemia (Orphanet:47)
Zunich-Kaye syndrome (Orphanet:3474)