Inflammatory abnormality of the skin

Symptom Information:

Symptom ID: HPO:0011123
Synonyms:
Abnormal tendency to infections of the skin [HPO:0011123]
Inflammatory skin disease [HPO:0011123]
Skin inflammation [HPO:0011123]
Inflammatory skin [Orphanet:23490]
Dermatitis (disorder) [Orphanet:23490]
Dermatitis [Orphanet:23490]
Cutaneous inflammation [Orphanet:23490]
Dermatitis [MedDRA:10012431]
Acrodermatitis [MedDRA:10012431]
Dermatitic reaction of face [MedDRA:10012431]
Dermatitic reaction of neck [MedDRA:10012431]
Dermatitis autosensitization [MedDRA:10012431]
Dermatitis due to other specified substances taken internally [MedDRA:10012431]
Dermatitis due to substances taken internally [MedDRA:10012431]
Dermatitis due to unspecified substance taken internally [MedDRA:10012431]
Dermatitis flare-up [MedDRA:10012431]
Dermatitis NOS [MedDRA:10012431]
Dermatitis NOS aggravated [MedDRA:10012431]
Dermatitis perioral [MedDRA:10012431]
Dermatitis simplex erythematosa [MedDRA:10012431]
Inflammation dorsum of left foot [MedDRA:10012431]
Peri-oral dermatitis [MedDRA:10012431]
Perioral dermatitis [MedDRA:10012431]
Rash and other nonspecific skin eruption [MedDRA:10012431]
Skin inflammation NOS [MedDRA:10012431]
Dermatitis (NOS) [MedDRA:10012431]
Roughness circumoral [MedDRA:10012431]
Dermatitis autosensitisation [MedDRA:10012431]
Skin inflammation [MedDRA:10012431]
Chronic hand dermatitis [MedDRA:10012431]
Interface dermatitis [MedDRA:10012431]
Dermatitis (chronic or chronically relapsing, major feature) [OMIM:Dermatitis (chronic or chronically relapsing, major feature)]
Interface dermatitis [OMIM:Interface dermatitis]
Quality:
Cross references:
Orphanet:23490 "Cutaneous inflammation" [Orphanet:23490]
OMIM: "Dermatitis (chronic or chronically relapsing, major feature)" [OMIM:Dermatitis (chronic or chronically relapsing, major feature)]
OMIM: "Interface dermatitis" [OMIM:Interface dermatitis]
UMLS:C0011603 "Dermatitis" [Orphanet:23490]
Is a (Direct Parents):
MedDRA Dermatitis and eczema
HPO         Abnormality of skin physiology
Orphanet Abnormality of the skin
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)
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)