Inflammatory abnormality of the skin
Symptom Information:
Symptom ID: | HPO:0011123 | |||||||||||||||||||||||||||||||||
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) Generalized abnormality of skin(HPO:0011354) Abnormality of skin physiology(HPO:0011122) Inflammatory abnormality of the skin(HPO:0011123) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Epidermal and dermal conditions(MedDRA:10014982) Dermatitis and eczema(MedDRA:10012435) Inflammatory abnormality of the skin(HPO:0011123) |
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Database Frequency: | 10 / 7739 | |||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
CHILBLAIN LUPUS 2 | (OMIM:614415) |
Cutaneous lupus erythematosus | (Orphanet:535) |
DERMATITIS, ATOPIC | (OMIM:603165) |
Keratosis pilaris atrophicans | (Orphanet:498) |
Kerion celsi | (Orphanet:499) |
Malakoplakia | (Orphanet:556) |
Melkersson-Rosenthal syndrome | (Orphanet:2483) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
Ulerythema ophryogenesis | (Orphanet:3406) |