Eczematoid dermatitis

Symptom Information:

Symptom ID: HPO:0000976
Synonyms:
Eczema [Orphanet:23230]
Eczema (disorder) [Orphanet:23230]
Eczema [HPO:0000976]
Eczematoid dermatitis [OMIM:Eczematoid dermatitis]
Eczema [MedDRA:10014184]
Dermatitis eczematoid [MedDRA:10014184]
Eczema (rash) in the outer ear [MedDRA:10014184]
Eczema acute [MedDRA:10014184]
Eczema aggravated [MedDRA:10014184]
Eczema exacerbated [MedDRA:10014184]
Eczema facial [MedDRA:10014184]
Eczema NOS [MedDRA:10014184]
Eczema of external auditory meatus [MedDRA:10014184]
Eczema papular [MedDRA:10014184]
Eczematous dermatitis [MedDRA:10014184]
Eczematous nipple [MedDRA:10014184]
Eczematous rash [MedDRA:10014184]
Erythematosquamous dermatosis [MedDRA:10014184]
Generalised eczematous reaction [MedDRA:10014184]
Other erythematosquamous dermatosis [MedDRA:10014184]
Reaction eczematous [MedDRA:10014184]
Scrotal eczema [MedDRA:10014184]
Generalized eczematous reaction [MedDRA:10014184]
Epiderma spongiosis [MedDRA:10014184]
Vulval eczema [MedDRA:10014184]
Chronic eczema [MedDRA:10014184]
Acute spongiotic dermatitis [MedDRA:10014184]
Subacute spongiotic dermatitis [MedDRA:10014184]
Eczema (8 of 23) [OMIM:Eczema (8 of 23)]
Eczema (face and flexural areas) [OMIM:Eczema (face and flexural areas)]
Eczema (in 1 patient) [OMIM:Eczema (in 1 patient)]
Eczema (in some patients) [OMIM:Eczema (in some patients)]
Eczema (perifollicular accentuation) [OMIM:Eczema (perifollicular accentuation)]
Eczema (rare) [OMIM:Eczema (rare)]
Eczematous dermatitis [OMIM:Eczematous dermatitis]
Quality:
Cross references:
HPO:0000964 "Eczema" [Orphanet:23230]
HPO:0001047 "Atopic dermatitis" [Orphanet:23230]
Orphanet:23230 "Eczema" [Orphanet:23230]
OMIM: "Eczematoid dermatitis" [OMIM:Eczematoid dermatitis]
OMIM: "Eczema (8 of 23)" [OMIM:Eczema (8 of 23)]
OMIM: "Eczema (face and flexural areas)" [OMIM:Eczema (face and flexural areas)]
OMIM: "Eczema (in 1 patient)" [OMIM:Eczema (in 1 patient)]
OMIM: "Eczema (in some patients)" [OMIM:Eczema (in some patients)]
OMIM: "Eczema (perifollicular accentuation)" [OMIM:Eczema (perifollicular accentuation)]
OMIM: "Eczema (rare)" [OMIM:Eczema (rare)]
OMIM: "Eczematous dermatitis" [OMIM:Eczematous dermatitis]
UMLS:C0013595 "Eczema" [HPO:0000976]
UMLS:C0013595 "Eczema" [Orphanet:23230]
Is a (Direct Parents):
MedDRA Dermatitis and eczema
HPO         Eczema
Orphanet Skin rash
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)
                      Eczema(HPO:0000964)
                         Eczematoid dermatitis(HPO:0000976)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Epidermal and dermal conditions(MedDRA:10014982)
       Dermatitis and eczema(MedDRA:10012435)
          Eczematoid dermatitis(HPO:0000976)
Database Frequency: 22 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Bazex-Dupré-Christol syndrome (Orphanet:113)
Classical mycosis fungoides (Orphanet:2584)
Classical phenylketonuria (Orphanet:79254)
Combined immunodeficiency due to ZAP70 deficiency (Orphanet:911)
Cranio-osteoarthropathy (Orphanet:1525)
DERMATITIS, ATOPIC (OMIM:603165)
Dubowitz syndrome (Orphanet:235)
EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED (OMIM:130090)
Extramammary Paget disease (Orphanet:2800)
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE (OMIM:233690)
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE,TYPE I (OMIM:233700)
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE,TYPE II (OMIM:233710)
GRANULOMATOUS DISEASE, CHRONIC, X-LINKED (OMIM:306400)
ICHTHYOSIS VULGARIS (OMIM:146700)
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome (Orphanet:37042)
Intellectual deficit - sparse hair - brachydactyly (Orphanet:3051)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 (OMIM:611091)
Maternal hyperphenylalaninemia (Orphanet:2209)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
Thymic aplasia (Orphanet:83471)