Eczema

Symptom Information:

Symptom ID: HPO:0000964
Synonyms:
Dermatitis [HPO:0000964]
Eczema (disorder) [Orphanet:23230]
Eczema [Orphanet:23230]
Dermatitis [OMIM:Dermatitis]
Eczema [OMIM:Eczema]
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]
Dermatitis (chronic or chronically relapsing, major feature) [OMIM:Dermatitis (chronic or chronically relapsing, major feature)]
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:0001047 "Atopic dermatitis" [Orphanet:23230]
HPO:0000976 "Eczematoid dermatitis" [Orphanet:23230]
Orphanet:23230 "Eczema" [Orphanet:23230]
OMIM: "Dermatitis" [OMIM:Dermatitis]
OMIM: "Eczema" [OMIM:Eczema]
OMIM: "Dermatitis (chronic or chronically relapsing, major feature)" [OMIM:Dermatitis (chronic or chronically relapsing, major feature)]
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:0000964]
UMLS:C0013595 "Eczema" [Orphanet:23230]
Is a (Direct Parents):
HPO         Inflammatory abnormality of the skin
Orphanet Skin rash
MedDRA Dermatitis and eczema
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)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Epidermal and dermal conditions(MedDRA:10014982)
       Dermatitis and eczema(MedDRA:10012435)
          Eczema(HPO:0000964)
Database Frequency: 81 / 7739
Resource:

All diseases associated with this symptom:

2q37 microdeletion syndrome (Orphanet:1001)
8q21.11 microdeletion syndrome (Orphanet:284160)
ADULT syndrome (Orphanet:978)
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET (OMIM:615952)
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V (OMIM:616100)
Autoimmune lymphoproliferative syndrome with recurrent infections (Orphanet:275517)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Autosomal dominant hypocalcemia (Orphanet:428)
Autosomal dominant hypohidrotic ectodermal dysplasia (Orphanet:1810)
Autosomal recessive hyper-IgE syndrome (Orphanet:169446)
Barth syndrome (Orphanet:111)
Bazex-Dupré-Christol syndrome (Orphanet:113)
Blau syndrome (Orphanet:90340)
Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency (Orphanet:329255)
Bullous pemphigoid (Orphanet:703)
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:212750)
Cataract - deafness - hypogonadism (Orphanet:1383)
Chronic granulomatous disease (Orphanet:379)
Classical mycosis fungoides (Orphanet:2584)
Classical phenylketonuria (Orphanet:79254)
Combined immunodeficiency due to DOCK8 deficiency (Orphanet:217390)
Cranio-osteoarthropathy (Orphanet:1525)
Cutis laxa (Orphanet:209)
DERMATITIS, ATOPIC (OMIM:603165)
Dermatitis herpetiformis (Orphanet:1656)
Dubowitz syndrome (Orphanet:235)
Dystrophic epidermolysis bullosa (Orphanet:303)
Ectodermal dysplasia syndrome (Orphanet:79373)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Epidermolytic palmoplantar keratoderma (Orphanet:2199)
Erythropoietic protoporphyria (Orphanet:79278)
Fukuda-Miyanomae-Nakata syndrome (Orphanet:2060)
Grubben-de Cock-Borghgraef syndrome (Orphanet:2101)
Hereditary acrokeratotic poikiloderma, Weary type (Orphanet:2907)
Hypohidrotic ectodermal dysplasia (Orphanet:238468)
IMMUNODEFICIENCY 17 (OMIM:615607)
IMMUNODEFICIENCY 23 (OMIM:615816)
IMMUNODEFICIENCY 31C (OMIM:614162)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
IgE RESPONSIVENESS, ATOPIC (OMIM:147050)
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome (Orphanet:37042)
Immunodeficiency due to CD25 deficiency (Orphanet:169100)
Intellectual deficit - sparse hair - brachydactyly (Orphanet:3051)
Intellectual deficit, X-linked - short stature - obesity (Orphanet:3055)
Isolated sulfite oxidase deficiency (Orphanet:99731)
Jacobsen syndrome (Orphanet:2308)
Keratosis follicularis spinulosa decalvans (Orphanet:2340)
Koolen-De Vries syndrome (Orphanet:96169)
LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA (OMIM:608809)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 (OMIM:611091)
MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUALAPPEARANCE (OMIM:612947)
Maternal hyperphenylalaninemia (Orphanet:2209)
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C (OMIM:613216)
Netherton syndrome (Orphanet:634)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
PELGER-HUET ANOMALY (OMIM:169400)
POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY (OMIM:615895)
Phenylketonuria (Orphanet:716)
Pityriasis rubra pilaris (Orphanet:2897)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Polyglucosan body myopathy type 1 (ORPHA:397937)
Porphyria cutanea tarda (Orphanet:101330)
Propionic acidemia (Orphanet:35)
Roifman syndrome (Orphanet:353298)
SENER SYNDROME (OMIM:606156)
SRD5A3-CDG (Orphanet:324737)
Say-Barber-Miller syndrome (Orphanet:3132)
Shwachman-Diamond syndrome (Orphanet:811)
Smith-Lemli-Opitz syndrome (Orphanet:818)
T-B+ severe combined immunodeficiency due to CD45 deficiency (Orphanet:169157)
T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency (Orphanet:169154)
TRICHORRHEXIS NODOSA SYNDROME (OMIM:275550)
W syndrome (Orphanet:2804)
WISKOTT-ALDRICH SYNDROME (OMIM:277970)
WISKOTT-ALDRICH SYNDROME (OMIM:301000)
WISKOTT-ALDRICH SYNDROME 2 (OMIM:614493)
WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM (OMIM:600903)
Wiskott-Aldrich syndrome (Orphanet:906)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)
X-linked thrombocytopenia with normal platelets (Orphanet:852)
ZINC DEFICIENCY, TRANSIENT NEONATAL (OMIM:608118)