Skin ulcer
Symptom Information:
Symptom ID: | HPO:0200042 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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 integument(HPO:0001574) Abnormality of the skin(HPO:0000951) Localized skin lesion(HPO:0011355) Skin ulcer(HPO:0200042) MedDRA: 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) |
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Database Frequency: | 138 / 7739 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
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) |
LEG ULCERS, FAMILIAL, OF JUVENILE ONSET | (OMIM:150590) |
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) |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC | (OMIM:613640) |
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) |